SLC2A11 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	SLC2A11
Entrez Gene ID	66035
Full Name	solute carrier family 2 member 11
Synonyms	GLUT10,GLUT11
General protein information	Preferred Names solute carrier family 2 member 11 Names solute carrier family 2, facilitated glucose transporter member 11 facilitative glucose transporter GLUT11 glucose transporter protein 10 glucose transporter protein 11 glucose transporter type 10 glucose transporter type 11 glucose transporter-like protein XI solute carrier family 2 (facilitated glucose transporter), member 11
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 22 Map Location: 22q11.23
Summary	This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013].
Disorder MIM:	610367

mRNA and Protein(s)

mRNA	Protein	Name
NM_001024938.4	NP_001020109.1	solute carrier family 2, facilitated glucose transporter member 11 isoform c
NM_001024938.3	NP_001020109.1	solute carrier family 2, facilitated glucose transporter member 11 isoform c
NM_001024939.3	NP_001020110.1	solute carrier family 2, facilitated glucose transporter member 11 isoform b
NM_001282864.1	NP_001269793.1	solute carrier family 2, facilitated glucose transporter member 11 isoform d
NM_030807.4	NP_110434.3	solute carrier family 2, facilitated glucose transporter member 11 isoform a
NM_001024939.4	NP_001020110.1	solute carrier family 2, facilitated glucose transporter member 11 isoform b
NM_030807.5	NP_110434.3	solute carrier family 2, facilitated glucose transporter member 11 isoform a

Pathways from BioSystems

Homologies

Xenopus tropicalis (tropical clawed frog)	slc2a11	XP_004910639.1
Homo sapiens (human)	SLC2A11	NP_110434.3
	SLC2A11	XP_001086712.1
Bos taurus (cattle)	SLC2A11	NP_001180026.1
Gallus gallus (chicken)	SLC2A11	XP_425279.2
Pan troglodytes (chimpanzee)	SLC2A11	XP_003317186.1
Canis lupus familiaris (dog)	SLC2A11	XP_543531.4
Danio rerio (zebrafish)	LOC560358	XP_688856.2

Gene Ontology
Bibliography

Related articles in PubMed

Multiple myeloma exhibits novel dependence on GLUT4, GLUT8, and GLUT11: implications for glucose transporter-directed therapy.
McBrayer SK, Cheng JC, Singhal S, Krett NL, Rosen ST, Shanmugam M
Blood119(20)4686-97(2012 May)

A highly conserved hydrophobic motif in the exofacial vestibule of fructose transporting SLC2A proteins acts as a critical determinant of their substrate selectivity.
Manolescu AR, Augustin R, Moley K, Cheeseman C
Molecular membrane biology24(5-6)455-63(2007 Sep-Dec)

Characterization of the human SLC2A11 (GLUT11) gene: alternative promoter usage, function, expression, and subcellular distribution of three isoforms, and lack of mouse orthologue.
Scheepers A, Schmidt S, Manolescu A, Cheeseman CI, Bell A, Zahn C, Joost HG, Sch?rmann A
Molecular membrane biology22(4)339-51(2005 Jul-Aug)

GLUT11, but not GLUT8 or GLUT12, is expressed in human skeletal muscle in a fibre type-specific pattern.
Gaster M, Handberg A, Sch?rmann A, Joost HG, Beck-Nielsen H, Schr?der HD
Pflugers Archiv : European journal of physiology448(1)105-13(2004 Apr)

Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues.
Wu X, Li W, Sharma V, Godzik A, Freeze HH
Molecular genetics and metabolism76(1)37-45(2002 May)

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Critical roles for novel GLUT family members highlight a therapeutic strategy entailing selective GLUT inhibition to specifically target aberrant glucose metabolism in cancer.
Title: Multiple myeloma exhibits novel dependence on GLUT4, GLUT8, and GLUT11: implications for glucose transporter-directed therapy.

Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)
Title: Polymorphisms in innate immunity genes and risk of childhood leukemia.

Observational study of gene-disease association. (HuGE Navigator)
Title: Risk of meningioma and common variation in genes related to innate immunity.

Observational study of gene-disease association. (HuGE Navigator)
Title: Common variation in genes related to innate immunity and risk of adult glioma.

GLUT11 can also transport fructose, but it has the motif DSV at the same position, which appears to function in the same manner as NXI and when all three residues are replaced with NAV fructose transport lost.
Title: A highly conserved hydrophobic motif in the exofacial vestibule of fructose transporting SLC2A proteins acts as a critical determinant of their substrate selectivity.

The following SLC2A11 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the SLC2A11 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1⁺/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

***CloneID	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu00721	NM_001024939.4 Latest version!	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
OHu07871	NM_030807.5 Latest version!	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$307.30 $439.00
OHu08461	NM_001282864.1 Latest version!	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 4, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$307.30 $439.00
OHu08722	NM_001024938.4 Latest version!	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
View Old Accession Versions >>
OHu08722	NM_001024938.3	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
OHu00721	NM_001024939.3	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
OHu07871	NM_030807.4	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$307.30 $439.00
Hide Old Accession Versions >>

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***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.

Reference Sequences (Refseq)

SLC2A11 ( NM_001024939.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020110.1 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu00721
Clone ID Related Accession (Same CDS sequence)	NM_001024939.3 , NM_001024939.4
Accession Version	NM_001024939.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1500bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2018-06-29
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC303452.1, AP000350.1 and AK092466.1. On Sep 20, 2013 this sequence version replaced NM_001024939.2. Transcript Variant: This variant (2, also known as SLC2A11-c) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (b) is shorter and has a distinct N-terminus, compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: SRR1803613.120305.1, SRR1803612.91305.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968968 [ECO:0000348] ##Evidence-Data-END##

ATGCTCCACG CCCTCCTGCG ATCTAGAATG ATTCAGGGCA GGATCCTGCT CCTGACCATC 
TGCGCTGCCG GCATTGGTGG GACTTTTCAG TTTGGCTATA ACCTCTCTAT CATCAATGCC 
CCGACCTTGC ACATTCAGGA ATTCACCAAT GAGACATGGC AGGCGCGTAC TGGAGAGCCA 
CTGCCCGATC ACCTAGTCCT GCTTATGTGG TCCCTCATCG TGTCTCTGTA TCCCCTGGGA 
GGCCTCTTTG GAGCACTGCT TGCAGGTCCC TTGGCCATCA CGCTGGGAAG GAAGAAGTCC 
CTCCTGGTGA ATAACATCTT TGTGGTGTCA GCAGCAATCC TGTTTGGATT CAGCCGCAAA 
GCAGGCTCCT TTGAGATGAT CATGCTGGGA AGACTGCTCG TGGGAGTCAA TGCAGGTGTG 
AGCATGAACA TCCAGCCCAT GTACCTGGGG GAGAGCGCCC CTAAGGAGCT CCGAGGAGCT 
GTGGCCATGA GCTCAGCCAT CTTTACGGCT CTGGGGATCG TGATGGGACA GGTGGTCGGA 
CTCAGGGAGC TCCTAGGTGG CCCTCAGGCC TGGCCCCTGC TGCTGGCCAG CTGCCTGGTG 
CCCGGGGCGC TCCAGCTCGC CTCCCTGCCT CTGCTCCCTG AAAGCCCGCG CTACCTCCTC 
ATTGACTGTG GAGACACCGA GGCCTGCCTG GCAGCACTAC GGCGGCTCCG GGGCTCCGGG 
GACTTGGCAG GGGAGCTGGA GGAGCTGGAG GAGGAGCGCG CTGCCTGCCA GGGCTGCCGT 
GCCCGGCGCC CATGGGAGCT GTTCCAGCAT CGGGCCCTGA GGAGACAGGT GACAAGCCTC 
GTGGTTCTGG GCAGTGCCAT GGAGCTCTGC GGGAATGACT CGGTGTACGC CTACGCCTCC 
TCCGTGTTCC GGAAGGCAGG AGTGCCGGAA GCGAAGATCC AGTACGCGAT CATCGGGACT 
GGGAGCTGCG AGCTGCTCAC GGCGGTTGTT AGTTGTGTGG TAATCGAGAG GGTGGGTCGG 
CGCGTGCTGC TCATCGGTGG GTACAGCCTG ATGACCTGCT GGGGGAGCAT CTTCACTGTG 
GCCCTGTGCC TGCAGAGCTC CTTCCCCTGG ACACTCTACC TGGCCATGGC CTGCATCTTT 
GCCTTCATCC TCAGCTTTGG CATTGGCCCT GCCGGAGTGA CGGGGATCCT GGCCACAGAG 
CTGTTTGACC AGATGGCCAG GCCTGCTGCC TGCATGGTCT GCGGGGCGCT CATGTGGATC 
ATGCTCATCC TGGTCGGCCT GGGATTTCCC TTTATCATGG AGGCCTTGTC CCACTTCCTC 
TATGTCCCTT TCCTTGGTGT CTGTGTCTGT GGGGCCATCT ACACTGGCCT GTTCCTTCCT 
GAGACCAAAG GCAAGACCTT CCAAGAGATC TCCAAGGAAT TACACAGACT CAACTTCCCC 
AGGCGGGCCC AGGGCCCCAC GTGGAGGAGC CTGGAGGTTA TCCAGTCAAC AGAACTCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001020110.1
CDS	148..1647
Translation	MLHALLRSRMIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_001024939.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001024939.3

ORF Insert Sequence:

ATGCTCCACG CCCTCCTGCG ATCTAGAATG ATTCAGGGCA GGATCCTGCT CCTGACCATC 
TGCGCTGCCG GCATTGGTGG GACTTTTCAG TTTGGCTATA ACCTCTCTAT CATCAATGCC 
CCGACCTTGC ACATTCAGGA ATTCACCAAT GAGACATGGC AGGCGCGTAC TGGAGAGCCA 
CTGCCCGATC ACCTAGTCCT GCTTATGTGG TCCCTCATCG TGTCTCTGTA TCCCCTGGGA 
GGCCTCTTTG GAGCACTGCT TGCAGGTCCC TTGGCCATCA CGCTGGGAAG GAAGAAGTCC 
CTCCTGGTGA ATAACATCTT TGTGGTGTCA GCAGCAATCC TGTTTGGATT CAGCCGCAAA 
GCAGGCTCCT TTGAGATGAT CATGCTGGGA AGACTGCTCG TGGGAGTCAA TGCAGGTGTG 
AGCATGAACA TCCAGCCCAT GTACCTGGGG GAGAGCGCCC CTAAGGAGCT CCGAGGAGCT 
GTGGCCATGA GCTCAGCCAT CTTTACGGCT CTGGGGATCG TGATGGGACA GGTGGTCGGA 
CTCAGGGAGC TCCTAGGTGG CCCTCAGGCC TGGCCCCTGC TGCTGGCCAG CTGCCTGGTG 
CCCGGGGCGC TCCAGCTCGC CTCCCTGCCT CTGCTCCCTG AAAGCCCGCG CTACCTCCTC 
ATTGACTGTG GAGACACCGA GGCCTGCCTG GCAGCACTAC GGCGGCTCCG GGGCTCCGGG 
GACTTGGCAG GGGAGCTGGA GGAGCTGGAG GAGGAGCGCG CTGCCTGCCA GGGCTGCCGT 
GCCCGGCGCC CATGGGAGCT GTTCCAGCAT CGGGCCCTGA GGAGACAGGT GACAAGCCTC 
GTGGTTCTGG GCAGTGCCAT GGAGCTCTGC GGGAATGACT CGGTGTACGC CTACGCCTCC 
TCCGTGTTCC GGAAGGCAGG AGTGCCGGAA GCGAAGATCC AGTACGCGAT CATCGGGACT 
GGGAGCTGCG AGCTGCTCAC GGCGGTTGTT AGTTGTGTGG TAATCGAGAG GGTGGGTCGG 
CGCGTGCTGC TCATCGGTGG GTACAGCCTG ATGACCTGCT GGGGGAGCAT CTTCACTGTG 
GCCCTGTGCC TGCAGAGCTC CTTCCCCTGG ACACTCTACC TGGCCATGGC CTGCATCTTT 
GCCTTCATCC TCAGCTTTGG CATTGGCCCT GCCGGAGTGA CGGGGATCCT GGCCACAGAG 
CTGTTTGACC AGATGGCCAG GCCTGCTGCC TGCATGGTCT GCGGGGCGCT CATGTGGATC 
ATGCTCATCC TGGTCGGCCT GGGATTTCCC TTTATCATGG AGGCCTTGTC CCACTTCCTC 
TATGTCCCTT TCCTTGGTGT CTGTGTCTGT GGGGCCATCT ACACTGGCCT GTTCCTTCCT 
GAGACCAAAG GCAAGACCTT CCAAGAGATC TCCAAGGAAT TACACAGACT CAACTTCCCC 
AGGCGGGCCC AGGGCCCCAC GTGGAGGAGC CTGGAGGTTA TCCAGTCAAC AGAACTCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_001024939.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020110.1 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu00721
Clone ID Related Accession (Same CDS sequence)	NM_001024939.3 , NM_001024939.4
Accession Version	NM_001024939.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1500bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-18
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC303452.1, AP000350.1 and AK092466.1. On Jun 2, 2019 this sequence version replaced NM_001024939.3. Transcript Variant: This variant (2, also known as SLC2A11-c) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (b) is shorter and has a distinct N-terminus, compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: SRR1803613.120305.1, SRR1803612.91305.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968968 [ECO:0000348] ##Evidence-Data-END##

ATGCTCCACG CCCTCCTGCG ATCTAGAATG ATTCAGGGCA GGATCCTGCT CCTGACCATC 
TGCGCTGCCG GCATTGGTGG GACTTTTCAG TTTGGCTATA ACCTCTCTAT CATCAATGCC 
CCGACCTTGC ACATTCAGGA ATTCACCAAT GAGACATGGC AGGCGCGTAC TGGAGAGCCA 
CTGCCCGATC ACCTAGTCCT GCTTATGTGG TCCCTCATCG TGTCTCTGTA TCCCCTGGGA 
GGCCTCTTTG GAGCACTGCT TGCAGGTCCC TTGGCCATCA CGCTGGGAAG GAAGAAGTCC 
CTCCTGGTGA ATAACATCTT TGTGGTGTCA GCAGCAATCC TGTTTGGATT CAGCCGCAAA 
GCAGGCTCCT TTGAGATGAT CATGCTGGGA AGACTGCTCG TGGGAGTCAA TGCAGGTGTG 
AGCATGAACA TCCAGCCCAT GTACCTGGGG GAGAGCGCCC CTAAGGAGCT CCGAGGAGCT 
GTGGCCATGA GCTCAGCCAT CTTTACGGCT CTGGGGATCG TGATGGGACA GGTGGTCGGA 
CTCAGGGAGC TCCTAGGTGG CCCTCAGGCC TGGCCCCTGC TGCTGGCCAG CTGCCTGGTG 
CCCGGGGCGC TCCAGCTCGC CTCCCTGCCT CTGCTCCCTG AAAGCCCGCG CTACCTCCTC 
ATTGACTGTG GAGACACCGA GGCCTGCCTG GCAGCACTAC GGCGGCTCCG GGGCTCCGGG 
GACTTGGCAG GGGAGCTGGA GGAGCTGGAG GAGGAGCGCG CTGCCTGCCA GGGCTGCCGT 
GCCCGGCGCC CATGGGAGCT GTTCCAGCAT CGGGCCCTGA GGAGACAGGT GACAAGCCTC 
GTGGTTCTGG GCAGTGCCAT GGAGCTCTGC GGGAATGACT CGGTGTACGC CTACGCCTCC 
TCCGTGTTCC GGAAGGCAGG AGTGCCGGAA GCGAAGATCC AGTACGCGAT CATCGGGACT 
GGGAGCTGCG AGCTGCTCAC GGCGGTTGTT AGTTGTGTGG TAATCGAGAG GGTGGGTCGG 
CGCGTGCTGC TCATCGGTGG GTACAGCCTG ATGACCTGCT GGGGGAGCAT CTTCACTGTG 
GCCCTGTGCC TGCAGAGCTC CTTCCCCTGG ACACTCTACC TGGCCATGGC CTGCATCTTT 
GCCTTCATCC TCAGCTTTGG CATTGGCCCT GCCGGAGTGA CGGGGATCCT GGCCACAGAG 
CTGTTTGACC AGATGGCCAG GCCTGCTGCC TGCATGGTCT GCGGGGCGCT CATGTGGATC 
ATGCTCATCC TGGTCGGCCT GGGATTTCCC TTTATCATGG AGGCCTTGTC CCACTTCCTC 
TATGTCCCTT TCCTTGGTGT CTGTGTCTGT GGGGCCATCT ACACTGGCCT GTTCCTTCCT 
GAGACCAAAG GCAAGACCTT CCAAGAGATC TCCAAGGAAT TACACAGACT CAACTTCCCC 
AGGCGGGCCC AGGGCCCCAC GTGGAGGAGC CTGGAGGTTA TCCAGTCAAC AGAACTCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001020110.1
CDS	126..1625
Translation	MLHALLRSRMIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_001024939.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001024939.4

ORF Insert Sequence:

ATGCTCCACG CCCTCCTGCG ATCTAGAATG ATTCAGGGCA GGATCCTGCT CCTGACCATC 
TGCGCTGCCG GCATTGGTGG GACTTTTCAG TTTGGCTATA ACCTCTCTAT CATCAATGCC 
CCGACCTTGC ACATTCAGGA ATTCACCAAT GAGACATGGC AGGCGCGTAC TGGAGAGCCA 
CTGCCCGATC ACCTAGTCCT GCTTATGTGG TCCCTCATCG TGTCTCTGTA TCCCCTGGGA 
GGCCTCTTTG GAGCACTGCT TGCAGGTCCC TTGGCCATCA CGCTGGGAAG GAAGAAGTCC 
CTCCTGGTGA ATAACATCTT TGTGGTGTCA GCAGCAATCC TGTTTGGATT CAGCCGCAAA 
GCAGGCTCCT TTGAGATGAT CATGCTGGGA AGACTGCTCG TGGGAGTCAA TGCAGGTGTG 
AGCATGAACA TCCAGCCCAT GTACCTGGGG GAGAGCGCCC CTAAGGAGCT CCGAGGAGCT 
GTGGCCATGA GCTCAGCCAT CTTTACGGCT CTGGGGATCG TGATGGGACA GGTGGTCGGA 
CTCAGGGAGC TCCTAGGTGG CCCTCAGGCC TGGCCCCTGC TGCTGGCCAG CTGCCTGGTG 
CCCGGGGCGC TCCAGCTCGC CTCCCTGCCT CTGCTCCCTG AAAGCCCGCG CTACCTCCTC 
ATTGACTGTG GAGACACCGA GGCCTGCCTG GCAGCACTAC GGCGGCTCCG GGGCTCCGGG 
GACTTGGCAG GGGAGCTGGA GGAGCTGGAG GAGGAGCGCG CTGCCTGCCA GGGCTGCCGT 
GCCCGGCGCC CATGGGAGCT GTTCCAGCAT CGGGCCCTGA GGAGACAGGT GACAAGCCTC 
GTGGTTCTGG GCAGTGCCAT GGAGCTCTGC GGGAATGACT CGGTGTACGC CTACGCCTCC 
TCCGTGTTCC GGAAGGCAGG AGTGCCGGAA GCGAAGATCC AGTACGCGAT CATCGGGACT 
GGGAGCTGCG AGCTGCTCAC GGCGGTTGTT AGTTGTGTGG TAATCGAGAG GGTGGGTCGG 
CGCGTGCTGC TCATCGGTGG GTACAGCCTG ATGACCTGCT GGGGGAGCAT CTTCACTGTG 
GCCCTGTGCC TGCAGAGCTC CTTCCCCTGG ACACTCTACC TGGCCATGGC CTGCATCTTT 
GCCTTCATCC TCAGCTTTGG CATTGGCCCT GCCGGAGTGA CGGGGATCCT GGCCACAGAG 
CTGTTTGACC AGATGGCCAG GCCTGCTGCC TGCATGGTCT GCGGGGCGCT CATGTGGATC 
ATGCTCATCC TGGTCGGCCT GGGATTTCCC TTTATCATGG AGGCCTTGTC CCACTTCCTC 
TATGTCCCTT TCCTTGGTGT CTGTGTCTGT GGGGCCATCT ACACTGGCCT GTTCCTTCCT 
GAGACCAAAG GCAAGACCTT CCAAGAGATC TCCAAGGAAT TACACAGACT CAACTTCCCC 
AGGCGGGCCC AGGGCCCCAC GTGGAGGAGC CTGGAGGTTA TCCAGTCAAC AGAACTCTAG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_030807.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_110434.3 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu07871
Clone ID Related Accession (Same CDS sequence)	NM_030807.4 , NM_030807.5
Accession Version	NM_030807.4	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1512bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2018-06-29
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA084206.1, AK314502.1, AJ271290.1, AK092466.1 and AP000350.1. On Sep 20, 2013 this sequence version replaced NM_030807.3. Transcript Variant: This variant (1, also known as SLC2A11-b) encodes isoform a (also known as GLUT11-L). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AF443201.1, AK314502.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2149398 [ECO:0000348] ##Evidence-Data-END##

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTTGTGT GGTAATCGAG 
AGGGTGGGTC GGCGCGTGCT GCTCATCGGT GGGTACAGCC TGATGACCTG CTGGGGGAGC 
ATCTTCACTG TGGCCCTGTG CCTGCAGAGC TCCTTCCCCT GGACACTCTA CCTGGCCATG 
GCCTGCATCT TTGCCTTCAT CCTCAGCTTT GGCATTGGCC CTGCCGGAGT GACGGGGATC 
CTGGCCACAG AGCTGTTTGA CCAGATGGCC AGGCCTGCTG CCTGCATGGT CTGCGGGGCG 
CTCATGTGGA TCATGCTCAT CCTGGTCGGC CTGGGATTTC CCTTTATCAT GGAGGCCTTG 
TCCCACTTCC TCTATGTCCC TTTCCTTGGT GTCTGTGTCT GTGGGGCCAT CTACACTGGC 
CTGTTCCTTC CTGAGACCAA AGGCAAGACC TTCCAAGAGA TCTCCAAGGA ATTACACAGA 
CTCAACTTCC CCAGGCGGGC CCAGGGCCCC ACGTGGAGGA GCCTGGAGGT TATCCAGTCA 
ACAGAACTCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_110434.3
CDS	359..1870
Translation	MEDELEPSLRPRTQIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_030807.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_030807.4

ORF Insert Sequence:

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTTGTGT GGTAATCGAG 
AGGGTGGGTC GGCGCGTGCT GCTCATCGGT GGGTACAGCC TGATGACCTG CTGGGGGAGC 
ATCTTCACTG TGGCCCTGTG CCTGCAGAGC TCCTTCCCCT GGACACTCTA CCTGGCCATG 
GCCTGCATCT TTGCCTTCAT CCTCAGCTTT GGCATTGGCC CTGCCGGAGT GACGGGGATC 
CTGGCCACAG AGCTGTTTGA CCAGATGGCC AGGCCTGCTG CCTGCATGGT CTGCGGGGCG 
CTCATGTGGA TCATGCTCAT CCTGGTCGGC CTGGGATTTC CCTTTATCAT GGAGGCCTTG 
TCCCACTTCC TCTATGTCCC TTTCCTTGGT GTCTGTGTCT GTGGGGCCAT CTACACTGGC 
CTGTTCCTTC CTGAGACCAA AGGCAAGACC TTCCAAGAGA TCTCCAAGGA ATTACACAGA 
CTCAACTTCC CCAGGCGGGC CCAGGGCCCC ACGTGGAGGA GCCTGGAGGT TATCCAGTCA 
ACAGAACTCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_030807.5 ) cDNA ORF clone, Homo sapiens(human) -> NP_110434.3 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.

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CloneID	OHu07871
Clone ID Related Accession (Same CDS sequence)	NM_030807.4 , NM_030807.5
Accession Version	NM_030807.5 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1512bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-19
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK314502.1, AJ271290.1, AK092466.1 and AP000350.1. On Jun 2, 2019 this sequence version replaced NM_030807.4. Transcript Variant: This variant (1, also known as SLC2A11-b) encodes isoform a (also known as GLUT11-L). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AF443201.1, AK314502.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2149398 [ECO:0000348] ##Evidence-Data-END##

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTTGTGT GGTAATCGAG 
AGGGTGGGTC GGCGCGTGCT GCTCATCGGT GGGTACAGCC TGATGACCTG CTGGGGGAGC 
ATCTTCACTG TGGCCCTGTG CCTGCAGAGC TCCTTCCCCT GGACACTCTA CCTGGCCATG 
GCCTGCATCT TTGCCTTCAT CCTCAGCTTT GGCATTGGCC CTGCCGGAGT GACGGGGATC 
CTGGCCACAG AGCTGTTTGA CCAGATGGCC AGGCCTGCTG CCTGCATGGT CTGCGGGGCG 
CTCATGTGGA TCATGCTCAT CCTGGTCGGC CTGGGATTTC CCTTTATCAT GGAGGCCTTG 
TCCCACTTCC TCTATGTCCC TTTCCTTGGT GTCTGTGTCT GTGGGGCCAT CTACACTGGC 
CTGTTCCTTC CTGAGACCAA AGGCAAGACC TTCCAAGAGA TCTCCAAGGA ATTACACAGA 
CTCAACTTCC CCAGGCGGGC CCAGGGCCCC ACGTGGAGGA GCCTGGAGGT TATCCAGTCA 
ACAGAACTCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_110434.3
CDS	128..1639
Translation	MEDELEPSLRPRTQIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_030807.5
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_030807.5

ORF Insert Sequence:

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTTGTGT GGTAATCGAG 
AGGGTGGGTC GGCGCGTGCT GCTCATCGGT GGGTACAGCC TGATGACCTG CTGGGGGAGC 
ATCTTCACTG TGGCCCTGTG CCTGCAGAGC TCCTTCCCCT GGACACTCTA CCTGGCCATG 
GCCTGCATCT TTGCCTTCAT CCTCAGCTTT GGCATTGGCC CTGCCGGAGT GACGGGGATC 
CTGGCCACAG AGCTGTTTGA CCAGATGGCC AGGCCTGCTG CCTGCATGGT CTGCGGGGCG 
CTCATGTGGA TCATGCTCAT CCTGGTCGGC CTGGGATTTC CCTTTATCAT GGAGGCCTTG 
TCCCACTTCC TCTATGTCCC TTTCCTTGGT GTCTGTGTCT GTGGGGCCAT CTACACTGGC 
CTGTTCCTTC CTGAGACCAA AGGCAAGACC TTCCAAGAGA TCTCCAAGGA ATTACACAGA 
CTCAACTTCC CCAGGCGGGC CCAGGGCCCC ACGTGGAGGA GCCTGGAGGT TATCCAGTCA 
ACAGAACTCT AG

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_001282864.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001269793.1 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 4, mRNA.

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CloneID	OHu08461
Clone ID Related Accession (Same CDS sequence)	NM_001282864.1
Accession Version	NM_001282864.1 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1608bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-15
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform d
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AP000350.1, AK300196.1 and AK092466.1. Transcript Variant: This variant (4) differs in the 5' UTR and contains multiple differences in the coding region, compared to variant 1, one of which results in a frameshift. The encoded isoform (d) is longer and has a distinct C- terminus, compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AK300196.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN04284274 [ECO:0000348] ##Evidence-Data-END##

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTGTAGC TGGGGTGGAT 
GAGGGCTGGG GGGTCCAGGC CGGGCTGACT TCCACCTCAC CCCCGCCCCG TCCACGGCAG 
AGCTCCTTCC CCTGGACACT CTACCTGGCC ATGGCCTGCA TCTTTGCCTT CATCCTCAGC 
TTTGGCATTG GCCCTGCCGG AGTGACGGGG ATCCTGGCCA CAGAGCTGTT TGACCAGATG 
GCCAGGCCTG CTGCCTGCAT GGTCTGCGGG GCGCTCATGT GGATCATGCT CATCCTGGTC 
GGCCTGGGAT TTCCCTTTAT CATGGTCTTG GGGTCTTTTT TAATCCGCAG GAGGCCTTGT 
CCCACTTCCT CTATGTCCCT TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC 
TGTTCCTTCC TGAGACCAAA GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC 
TCAACTTCCC CAGGCGGGCC CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA 
CAGAACTCTA GTCCCAAAGG GGTGGCCAGA GCCAAAGCCA GCTACTGTCC TGTCCTCTGC 
TTCCTGCCAG GGCCCTGGTC CTCACTCCCT CCTGCATTCC TCATTTAA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001269793.1
CDS	491..2098
Translation	MEDELEPSLRPRTQIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSVAGVDEGWGVQAGLTSTSPPPRPRQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMVLGSFLIRRRPCPTSSMSLSLVSVSVGPSTLACSFLRPKARPSKRSPRNYTDSTSPGGPRAPRGGAWRLSSQQNSSPKGVARAKASYCPVLCFLPGPWSSLPPAFLI

Target ORF information:

RefSeq Version	NM_001282864.1
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 4, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001282864.1

ORF Insert Sequence:

ATGGAGGATG AACTGGAGCC GTCCTTACGG CCTCGGACGC AGATTCAGGG CAGGATCCTG 
CTCCTGACCA TCTGCGCTGC CGGCATTGGT GGGACTTTTC AGTTTGGCTA TAACCTCTCT 
ATCATCAATG CCCCGACCTT GCACATTCAG GAATTCACCA ATGAGACATG GCAGGCGCGT 
ACTGGAGAGC CACTGCCCGA TCACCTAGTC CTGCTTATGT GGTCCCTCAT CGTGTCTCTG 
TATCCCCTGG GAGGCCTCTT TGGAGCACTG CTTGCAGGTC CCTTGGCCAT CACGCTGGGA 
AGGAAGAAGT CCCTCCTGGT GAATAACATC TTTGTGGTGT CAGCAGCAAT CCTGTTTGGA 
TTCAGCCGCA AAGCAGGCTC CTTTGAGATG ATCATGCTGG GAAGACTGCT CGTGGGAGTC 
AATGCAGGTG TGAGCATGAA CATCCAGCCC ATGTACCTGG GGGAGAGCGC CCCTAAGGAG 
CTCCGAGGAG CTGTGGCCAT GAGCTCAGCC ATCTTTACGG CTCTGGGGAT CGTGATGGGA 
CAGGTGGTCG GACTCAGGGA GCTCCTAGGT GGCCCTCAGG CCTGGCCCCT GCTGCTGGCC 
AGCTGCCTGG TGCCCGGGGC GCTCCAGCTC GCCTCCCTGC CTCTGCTCCC TGAAAGCCCG 
CGCTACCTCC TCATTGACTG TGGAGACACC GAGGCCTGCC TGGCAGCACT ACGGCGGCTC 
CGGGGCTCCG GGGACTTGGC AGGGGAGCTG GAGGAGCTGG AGGAGGAGCG CGCTGCCTGC 
CAGGGCTGCC GTGCCCGGCG CCCATGGGAG CTGTTCCAGC ATCGGGCCCT GAGGAGACAG 
GTGACAAGCC TCGTGGTTCT GGGCAGTGCC ATGGAGCTCT GCGGGAATGA CTCGGTGTAC 
GCCTACGCCT CCTCCGTGTT CCGGAAGGCA GGAGTGCCGG AAGCGAAGAT CCAGTACGCG 
ATCATCGGGA CTGGGAGCTG CGAGCTGCTC ACGGCGGTTG TTAGTGTAGC TGGGGTGGAT 
GAGGGCTGGG GGGTCCAGGC CGGGCTGACT TCCACCTCAC CCCCGCCCCG TCCACGGCAG 
AGCTCCTTCC CCTGGACACT CTACCTGGCC ATGGCCTGCA TCTTTGCCTT CATCCTCAGC 
TTTGGCATTG GCCCTGCCGG AGTGACGGGG ATCCTGGCCA CAGAGCTGTT TGACCAGATG 
GCCAGGCCTG CTGCCTGCAT GGTCTGCGGG GCGCTCATGT GGATCATGCT CATCCTGGTC 
GGCCTGGGAT TTCCCTTTAT CATGGTCTTG GGGTCTTTTT TAATCCGCAG GAGGCCTTGT 
CCCACTTCCT CTATGTCCCT TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC 
TGTTCCTTCC TGAGACCAAA GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC 
TCAACTTCCC CAGGCGGGCC CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA 
CAGAACTCTA GTCCCAAAGG GGTGGCCAGA GCCAAAGCCA GCTACTGTCC TGTCCTCTGC 
TTCCTGCCAG GGCCCTGGTC CTCACTCCCT CCTGCATTCC TCATTTAA

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_001024938.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020109.1 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.

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CloneID	OHu08722
Clone ID Related Accession (Same CDS sequence)	NM_001024938.4 , NM_001024938.3
Accession Version	NM_001024938.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1491bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-11-18
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform c
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK075467.1, BC018967.2 and AP000350.1. On Jun 2, 2019 this sequence version replaced NM_001024938.3. Transcript Variant: This variant (3, also known as SLC2A11-a) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate upstream start codon, compared to variant 1. The encoded isoform (c, also known as GLUT11-S) is shorter and has a distinct N-terminus, compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AK075467.1, SRR1803617.157290.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968968 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## RefSeq Select criteria :: based on conservation, expression ##RefSeq-Attributes-END##

ATGAGAGCGC TCCGAAGACT GATTCAGGGC AGGATCCTGC TCCTGACCAT CTGCGCTGCC 
GGCATTGGTG GGACTTTTCA GTTTGGCTAT AACCTCTCTA TCATCAATGC CCCGACCTTG 
CACATTCAGG AATTCACCAA TGAGACATGG CAGGCGCGTA CTGGAGAGCC ACTGCCCGAT 
CACCTAGTCC TGCTTATGTG GTCCCTCATC GTGTCTCTGT ATCCCCTGGG AGGCCTCTTT 
GGAGCACTGC TTGCAGGTCC CTTGGCCATC ACGCTGGGAA GGAAGAAGTC CCTCCTGGTG 
AATAACATCT TTGTGGTGTC AGCAGCAATC CTGTTTGGAT TCAGCCGCAA AGCAGGCTCC 
TTTGAGATGA TCATGCTGGG AAGACTGCTC GTGGGAGTCA ATGCAGGTGT GAGCATGAAC 
ATCCAGCCCA TGTACCTGGG GGAGAGCGCC CCTAAGGAGC TCCGAGGAGC TGTGGCCATG 
AGCTCAGCCA TCTTTACGGC TCTGGGGATC GTGATGGGAC AGGTGGTCGG ACTCAGGGAG 
CTCCTAGGTG GCCCTCAGGC CTGGCCCCTG CTGCTGGCCA GCTGCCTGGT GCCCGGGGCG 
CTCCAGCTCG CCTCCCTGCC TCTGCTCCCT GAAAGCCCGC GCTACCTCCT CATTGACTGT 
GGAGACACCG AGGCCTGCCT GGCAGCACTA CGGCGGCTCC GGGGCTCCGG GGACTTGGCA 
GGGGAGCTGG AGGAGCTGGA GGAGGAGCGC GCTGCCTGCC AGGGCTGCCG TGCCCGGCGC 
CCATGGGAGC TGTTCCAGCA TCGGGCCCTG AGGAGACAGG TGACAAGCCT CGTGGTTCTG 
GGCAGTGCCA TGGAGCTCTG CGGGAATGAC TCGGTGTACG CCTACGCCTC CTCCGTGTTC 
CGGAAGGCAG GAGTGCCGGA AGCGAAGATC CAGTACGCGA TCATCGGGAC TGGGAGCTGC 
GAGCTGCTCA CGGCGGTTGT TAGTTGTGTG GTAATCGAGA GGGTGGGTCG GCGCGTGCTG 
CTCATCGGTG GGTACAGCCT GATGACCTGC TGGGGGAGCA TCTTCACTGT GGCCCTGTGC 
CTGCAGAGCT CCTTCCCCTG GACACTCTAC CTGGCCATGG CCTGCATCTT TGCCTTCATC 
CTCAGCTTTG GCATTGGCCC TGCCGGAGTG ACGGGGATCC TGGCCACAGA GCTGTTTGAC 
CAGATGGCCA GGCCTGCTGC CTGCATGGTC TGCGGGGCGC TCATGTGGAT CATGCTCATC 
CTGGTCGGCC TGGGATTTCC CTTTATCATG GAGGCCTTGT CCCACTTCCT CTATGTCCCT 
TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC TGTTCCTTCC TGAGACCAAA 
GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC TCAACTTCCC CAGGCGGGCC 
CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA CAGAACTCTA G

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001020109.1
CDS	38..1528
Translation	MRALRRLIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_001024938.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001024938.4

ORF Insert Sequence:

ATGAGAGCGC TCCGAAGACT GATTCAGGGC AGGATCCTGC TCCTGACCAT CTGCGCTGCC 
GGCATTGGTG GGACTTTTCA GTTTGGCTAT AACCTCTCTA TCATCAATGC CCCGACCTTG 
CACATTCAGG AATTCACCAA TGAGACATGG CAGGCGCGTA CTGGAGAGCC ACTGCCCGAT 
CACCTAGTCC TGCTTATGTG GTCCCTCATC GTGTCTCTGT ATCCCCTGGG AGGCCTCTTT 
GGAGCACTGC TTGCAGGTCC CTTGGCCATC ACGCTGGGAA GGAAGAAGTC CCTCCTGGTG 
AATAACATCT TTGTGGTGTC AGCAGCAATC CTGTTTGGAT TCAGCCGCAA AGCAGGCTCC 
TTTGAGATGA TCATGCTGGG AAGACTGCTC GTGGGAGTCA ATGCAGGTGT GAGCATGAAC 
ATCCAGCCCA TGTACCTGGG GGAGAGCGCC CCTAAGGAGC TCCGAGGAGC TGTGGCCATG 
AGCTCAGCCA TCTTTACGGC TCTGGGGATC GTGATGGGAC AGGTGGTCGG ACTCAGGGAG 
CTCCTAGGTG GCCCTCAGGC CTGGCCCCTG CTGCTGGCCA GCTGCCTGGT GCCCGGGGCG 
CTCCAGCTCG CCTCCCTGCC TCTGCTCCCT GAAAGCCCGC GCTACCTCCT CATTGACTGT 
GGAGACACCG AGGCCTGCCT GGCAGCACTA CGGCGGCTCC GGGGCTCCGG GGACTTGGCA 
GGGGAGCTGG AGGAGCTGGA GGAGGAGCGC GCTGCCTGCC AGGGCTGCCG TGCCCGGCGC 
CCATGGGAGC TGTTCCAGCA TCGGGCCCTG AGGAGACAGG TGACAAGCCT CGTGGTTCTG 
GGCAGTGCCA TGGAGCTCTG CGGGAATGAC TCGGTGTACG CCTACGCCTC CTCCGTGTTC 
CGGAAGGCAG GAGTGCCGGA AGCGAAGATC CAGTACGCGA TCATCGGGAC TGGGAGCTGC 
GAGCTGCTCA CGGCGGTTGT TAGTTGTGTG GTAATCGAGA GGGTGGGTCG GCGCGTGCTG 
CTCATCGGTG GGTACAGCCT GATGACCTGC TGGGGGAGCA TCTTCACTGT GGCCCTGTGC 
CTGCAGAGCT CCTTCCCCTG GACACTCTAC CTGGCCATGG CCTGCATCTT TGCCTTCATC 
CTCAGCTTTG GCATTGGCCC TGCCGGAGTG ACGGGGATCC TGGCCACAGA GCTGTTTGAC 
CAGATGGCCA GGCCTGCTGC CTGCATGGTC TGCGGGGCGC TCATGTGGAT CATGCTCATC 
CTGGTCGGCC TGGGATTTCC CTTTATCATG GAGGCCTTGT CCCACTTCCT CTATGTCCCT 
TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC TGTTCCTTCC TGAGACCAAA 
GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC TCAACTTCCC CAGGCGGGCC 
CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA CAGAACTCTA G

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

SLC2A11 ( NM_001024938.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_001020109.1 Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.

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CloneID	OHu08722
Clone ID Related Accession (Same CDS sequence)	NM_001024938.4 , NM_001024938.3
Accession Version	NM_001024938.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1491bp) Protein sequence SNP
Vector	pcDNA3.1-C-(k)DYK or customized vector	User Manual
Clone information	Clone Map	MSDS
Tag on pcDNA3.1⁺/C-(K)DYK	C terminal DYKDDDDK tags
ORF Insert Method	CloneEZ™ Seamless cloning technology
Insert Structure	linear
Update Date	2019-02-23
Organism	Homo sapiens(human)
Product	solute carrier family 2, facilitated glucose transporter member 11 isoform c
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DA084206.1, AK075467.1, BC018967.2 and AP000350.1. On Sep 20, 2013 this sequence version replaced NM_001024938.2. Transcript Variant: This variant (3, also known as SLC2A11-a) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate upstream start codon, compared to variant 1. The encoded isoform (c, also known as GLUT11-S) is shorter and has a distinct N-terminus, compared to isoform a. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AK075467.1, SRR1803617.157290.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968540, SAMEA1968968 [ECO:0000348] ##Evidence-Data-END##

ATGAGAGCGC TCCGAAGACT GATTCAGGGC AGGATCCTGC TCCTGACCAT CTGCGCTGCC 
GGCATTGGTG GGACTTTTCA GTTTGGCTAT AACCTCTCTA TCATCAATGC CCCGACCTTG 
CACATTCAGG AATTCACCAA TGAGACATGG CAGGCGCGTA CTGGAGAGCC ACTGCCCGAT 
CACCTAGTCC TGCTTATGTG GTCCCTCATC GTGTCTCTGT ATCCCCTGGG AGGCCTCTTT 
GGAGCACTGC TTGCAGGTCC CTTGGCCATC ACGCTGGGAA GGAAGAAGTC CCTCCTGGTG 
AATAACATCT TTGTGGTGTC AGCAGCAATC CTGTTTGGAT TCAGCCGCAA AGCAGGCTCC 
TTTGAGATGA TCATGCTGGG AAGACTGCTC GTGGGAGTCA ATGCAGGTGT GAGCATGAAC 
ATCCAGCCCA TGTACCTGGG GGAGAGCGCC CCTAAGGAGC TCCGAGGAGC TGTGGCCATG 
AGCTCAGCCA TCTTTACGGC TCTGGGGATC GTGATGGGAC AGGTGGTCGG ACTCAGGGAG 
CTCCTAGGTG GCCCTCAGGC CTGGCCCCTG CTGCTGGCCA GCTGCCTGGT GCCCGGGGCG 
CTCCAGCTCG CCTCCCTGCC TCTGCTCCCT GAAAGCCCGC GCTACCTCCT CATTGACTGT 
GGAGACACCG AGGCCTGCCT GGCAGCACTA CGGCGGCTCC GGGGCTCCGG GGACTTGGCA 
GGGGAGCTGG AGGAGCTGGA GGAGGAGCGC GCTGCCTGCC AGGGCTGCCG TGCCCGGCGC 
CCATGGGAGC TGTTCCAGCA TCGGGCCCTG AGGAGACAGG TGACAAGCCT CGTGGTTCTG 
GGCAGTGCCA TGGAGCTCTG CGGGAATGAC TCGGTGTACG CCTACGCCTC CTCCGTGTTC 
CGGAAGGCAG GAGTGCCGGA AGCGAAGATC CAGTACGCGA TCATCGGGAC TGGGAGCTGC 
GAGCTGCTCA CGGCGGTTGT TAGTTGTGTG GTAATCGAGA GGGTGGGTCG GCGCGTGCTG 
CTCATCGGTG GGTACAGCCT GATGACCTGC TGGGGGAGCA TCTTCACTGT GGCCCTGTGC 
CTGCAGAGCT CCTTCCCCTG GACACTCTAC CTGGCCATGG CCTGCATCTT TGCCTTCATC 
CTCAGCTTTG GCATTGGCCC TGCCGGAGTG ACGGGGATCC TGGCCACAGA GCTGTTTGAC 
CAGATGGCCA GGCCTGCTGC CTGCATGGTC TGCGGGGCGC TCATGTGGAT CATGCTCATC 
CTGGTCGGCC TGGGATTTCC CTTTATCATG GAGGCCTTGT CCCACTTCCT CTATGTCCCT 
TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC TGTTCCTTCC TGAGACCAAA 
GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC TCAACTTCCC CAGGCGGGCC 
CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA CAGAACTCTA G

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

RefSeq	NP_001020109.1
CDS	269..1759
Translation	MRALRRLIQGRILLLTICAAGIGGTFQFGYNLSIINAPTLHIQEFTNETWQARTGEPLPDHLVLLMWSLIVSLYPLGGLFGALLAGPLAITLGRKKSLLVNNIFVVSAAILFGFSRKAGSFEMIMLGRLLVGVNAGVSMNIQPMYLGESAPKELRGAVAMSSAIFTALGIVMGQVVGLRELLGGPQAWPLLLASCLVPGALQLASLPLLPESPRYLLIDCGDTEACLAALRRLRGSGDLAGELEELEEERAACQGCRARRPWELFQHRALRRQVTSLVVLGSAMELCGNDSVYAYASSVFRKAGVPEAKIQYAIIGTGSCELLTAVVSCVVIERVGRRVLLIGGYSLMTCWGSIFTVALCLQSSFPWTLYLAMACIFAFILSFGIGPAGVTGILATELFDQMARPAACMVCGALMWIMLILVGLGFPFIMEALSHFLYVPFLGVCVCGAIYTGLFLPETKGKTFQEISKELHRLNFPRRAQGPTWRSLEVIQSTEL

Target ORF information:

RefSeq Version	NM_001024938.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 2 member 11 (SLC2A11), transcript variant 3, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001024938.3

ORF Insert Sequence:

ATGAGAGCGC TCCGAAGACT GATTCAGGGC AGGATCCTGC TCCTGACCAT CTGCGCTGCC 
GGCATTGGTG GGACTTTTCA GTTTGGCTAT AACCTCTCTA TCATCAATGC CCCGACCTTG 
CACATTCAGG AATTCACCAA TGAGACATGG CAGGCGCGTA CTGGAGAGCC ACTGCCCGAT 
CACCTAGTCC TGCTTATGTG GTCCCTCATC GTGTCTCTGT ATCCCCTGGG AGGCCTCTTT 
GGAGCACTGC TTGCAGGTCC CTTGGCCATC ACGCTGGGAA GGAAGAAGTC CCTCCTGGTG 
AATAACATCT TTGTGGTGTC AGCAGCAATC CTGTTTGGAT TCAGCCGCAA AGCAGGCTCC 
TTTGAGATGA TCATGCTGGG AAGACTGCTC GTGGGAGTCA ATGCAGGTGT GAGCATGAAC 
ATCCAGCCCA TGTACCTGGG GGAGAGCGCC CCTAAGGAGC TCCGAGGAGC TGTGGCCATG 
AGCTCAGCCA TCTTTACGGC TCTGGGGATC GTGATGGGAC AGGTGGTCGG ACTCAGGGAG 
CTCCTAGGTG GCCCTCAGGC CTGGCCCCTG CTGCTGGCCA GCTGCCTGGT GCCCGGGGCG 
CTCCAGCTCG CCTCCCTGCC TCTGCTCCCT GAAAGCCCGC GCTACCTCCT CATTGACTGT 
GGAGACACCG AGGCCTGCCT GGCAGCACTA CGGCGGCTCC GGGGCTCCGG GGACTTGGCA 
GGGGAGCTGG AGGAGCTGGA GGAGGAGCGC GCTGCCTGCC AGGGCTGCCG TGCCCGGCGC 
CCATGGGAGC TGTTCCAGCA TCGGGCCCTG AGGAGACAGG TGACAAGCCT CGTGGTTCTG 
GGCAGTGCCA TGGAGCTCTG CGGGAATGAC TCGGTGTACG CCTACGCCTC CTCCGTGTTC 
CGGAAGGCAG GAGTGCCGGA AGCGAAGATC CAGTACGCGA TCATCGGGAC TGGGAGCTGC 
GAGCTGCTCA CGGCGGTTGT TAGTTGTGTG GTAATCGAGA GGGTGGGTCG GCGCGTGCTG 
CTCATCGGTG GGTACAGCCT GATGACCTGC TGGGGGAGCA TCTTCACTGT GGCCCTGTGC 
CTGCAGAGCT CCTTCCCCTG GACACTCTAC CTGGCCATGG CCTGCATCTT TGCCTTCATC 
CTCAGCTTTG GCATTGGCCC TGCCGGAGTG ACGGGGATCC TGGCCACAGA GCTGTTTGAC 
CAGATGGCCA GGCCTGCTGC CTGCATGGTC TGCGGGGCGC TCATGTGGAT CATGCTCATC 
CTGGTCGGCC TGGGATTTCC CTTTATCATG GAGGCCTTGT CCCACTTCCT CTATGTCCCT 
TTCCTTGGTG TCTGTGTCTG TGGGGCCATC TACACTGGCC TGTTCCTTCC TGAGACCAAA 
GGCAAGACCT TCCAAGAGAT CTCCAAGGAA TTACACAGAC TCAACTTCCC CAGGCGGGCC 
CAGGGCCCCA CGTGGAGGAG CCTGGAGGTT ATCCAGTCAA CAGAACTCTA G

The stop codons will be deleted if pcDNA3.1⁺/C-(K)DYK vector is selected.

PubMed

Multiple myeloma exhibits novel dependence on GLUT4, GLUT8, and GLUT11: implications for glucose transporter-directed therapy.
Blood119(20)4686-97(2012 May)
McBrayer SK,Cheng JC,Singhal S,Krett NL,Rosen ST,Shanmugam M

A highly conserved hydrophobic motif in the exofacial vestibule of fructose transporting SLC2A proteins acts as a critical determinant of their substrate selectivity.
Molecular membrane biology24(5-6)455-63(2007 Sep-Dec)
Manolescu AR,Augustin R,Moley K,Cheeseman C

Characterization of the human SLC2A11 (GLUT11) gene: alternative promoter usage, function, expression, and subcellular distribution of three isoforms, and lack of mouse orthologue.
Molecular membrane biology22(4)339-51(2005 Jul-Aug)
Scheepers A,Schmidt S,Manolescu A,Cheeseman CI,Bell A,Zahn C,Joost HG,Sch?rmann A

GLUT11, but not GLUT8 or GLUT12, is expressed in human skeletal muscle in a fibre type-specific pattern.
Pflugers Archiv : European journal of physiology448(1)105-13(2004 Apr)
Gaster M,Handberg A,Sch?rmann A,Joost HG,Beck-Nielsen H,Schr?der HD

Cloning and characterization of glucose transporter 11, a novel sugar transporter that is alternatively spliced in various tissues.
Molecular genetics and metabolism76(1)37-45(2002 May)
Wu X,Li W,Sharma V,Godzik A,Freeze HH

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SLC2A11 cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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