SLC26A1 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	SLC26A1
Entrez Gene ID	10861
Full Name	solute carrier family 26 member 1
Synonyms	CAON,EDM4,SAT-1,SAT1
General protein information	Preferred Names solute carrier family 26 member 1 Names sulfate anion transporter 1 solute carrier family 26 (anion exchanger), member 1 solute carrier family 26 (sulfate transporter), member 1 sulfate anion tranporter AT1 sulfate/anion transporter SAT-1 protein
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 4 Map Location: 4p16.3
Summary	This gene is a member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures, but have markedly different tissue expression patterns. This gene is primarily expressed in the liver, pancreas, and brain. Three splice variants that encode different isoforms have been identified. [provided by RefSeq, Jul 2008].
Disorder MIM:	610130
Disorder Html:	?Nephrolithiasis, calcium oxalate, 167030 (3)

mRNA and Protein(s)

mRNA	Protein	Name
NM_134425.2	NP_602297.1	sulfate anion transporter 1 isoform b
NM_134425.3	NP_602297.1	sulfate anion transporter 1 isoform b
NM_213613.3	NP_998778.1	sulfate anion transporter 1 isoform a
NM_022042.3	NP_071325.2	sulfate anion transporter 1 isoform a
NM_213613.4	NP_998778.1	sulfate anion transporter 1 isoform a
NM_022042.4	NP_071325.2	sulfate anion transporter 1 isoform a

Pathways from BioSystems

Homologies

Pan troglodytes (chimpanzee)	SLC26A1	XP_003310259.1
Mus musculus (house mouse)	Slc26a1	NP_777359.3
Rattus norvegicus (Norway rat)	Slc26a1	NP_071623.2
Caenorhabditis elegans (roundworm)	sulp-2	NP_508944.1
Homo sapiens (human)	SLC26A1	NP_071325.2
Canis lupus familiaris (dog)	SLC26A1	XP_545984.3
Bos taurus (cattle)	SLC26A1	XP_005208341.1
	SLC26A1	XP_001093208.2

Gene Ontology
Bibliography

Related articles in PubMed

From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.
Tise CG, Perry JA, Anforth LE, Pavlovich MA, Backman JD, Ryan KA, Lewis JP, O'Connell JR, Yerges-Armstrong LM, Shuldiner AR
G3 (Bethesda, Md.)6(9)2909-18(2016 09)

Extracellular Cl(-) regulates human SO4 (2-)/anion exchanger SLC26A1 by altering pH sensitivity of anion transport.
Wu M, Heneghan JF, Vandorpe DH, Escobar LI, Wu BL, Alper SL
Pflugers Archiv : European journal of physiology468(8)1311-32(2016 Aug)

Mutations in SLC26A1 Cause Nephrolithiasis.
Gee HY, Jun I, Braun DA, Lawson JA, Halbritter J, Shril S, Nelson CP, Tan W, Stein D, Wassner AJ, Ferguson MA, Gucev Z, Sayer JA, Milosevic D, Baum M, Tasic V, Lee MG, Hildebrandt F
American journal of human genetics98(6)1228-1234(2016 Jun)

N-glycosylation and topology of the human SLC26 family of anion transport membrane proteins.
Li J, Xia F, Reithmeier RA
American journal of physiology. Cell physiology306(10)C943-60(2014 May)

Human SLC26A1 gene variants: a pilot study.
Dawson PA, Sim P, Mudge DW, Cowley D
TheScientificWorldJournal2013541710(2013)

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

SLC26A1 L348P was associated with lower whole-body bone mineral density (BMD) and higher serum calcium, consistent with the osteochondrodysplasia exhibited by dogs and sheep with naturally occurring, homozygous, loss-of-function mutations in Slc13a1
Title: From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.

Human SLC26A1 resembles SLC26 paralogs in its inhibition.
Title: Extracellular Cl(-) regulates human SO4 (2-)/anion exchanger SLC26A1 by altering pH sensitivity of anion transport.

Mutations in SLC26A1 gene is associated with Nephrolithiasis.
Title: Mutations in SLC26A1 Cause Nephrolithiasis.

SLC26A1 protein,point mutation is highly responsible for the hearing loss of newborns.
Title: Newborn genetic screening for high risk deafness-associated mutations with a new Tetra-primer ARMS PCR kit.

Screened the SLC26A1 gene in a cohort of 13 individuals with recurrent calcium oxalate urolithiasis, which is the commonest type. DNA sequence analyses showed missense mutations in seven patients.
Title: Human SLC26A1 gene variants: a pilot study.

The following SLC26A1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the SLC26A1 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)
OHu27594	NM_134425.3 Latest version!	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$134.50-$188.30 $269.00
OHu27619	NM_213613.4 Latest version!	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	12-14	$391.30 $559.00
OHu27619	NM_022042.4 Latest version!	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	12-14	$391.30 $559.00
View Old Accession Versions >>
OHu27594	NM_134425.2	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$134.50-$188.30 $269.00
OHu27619	NM_213613.3	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	12-14	$391.30 $559.00
OHu27619	NM_022042.3	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	12-14	$391.30 $559.00
Hide Old Accession Versions >>

ORF Online Only Promotion

Next-day Shipping ORF Clones ( in default vector with tag)
1 Clone	30% OFF
2-4 Clone	40% OFF
5 or more Clone	50% OFF
All Other ORF Clones
30% OFF

*Business Day

** You may select a custom vector to replace pcDNA3.1+/C-(K)DYK after clone is added to cart.

** GenScript guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories. In addition, please pay attention to the signal peptide, propeptide and transit peptide in target ORF, which may affect the choice of vector (N/C terminal tag vector).

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

Reference Sequences (Refseq)

SLC26A1 ( NM_134425.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_602297.1 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu27594
Clone ID Related Accession (Same CDS sequence)	NM_134425.2 , NM_134425.3
Accession Version	NM_134425.2	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 675bp) 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	sulfate anion transporter 1 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292747.1 and BC015517.2. This sequence is a reference standard in the RefSeqGene project. On Jun 28, 2013 this sequence version replaced NM_134425.1. Transcript Variant: This variant (2) lacks an exon in the 5' UTR and has an alternate 3' terminal exon, as compared to variant 3. It encodes isoform b which has a shorter and different C-terminus compared to isoform a. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC015517.2, BE787840.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN04284274 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGACGT CCTGGGGTAG AAACAGCTTC 
CAGCAACACC CATGGCAATT AACACAGAGG AGTGACTCGC AGGAACTTCT GGAAGAGGAG 
GAAAGATCTT GCTGA

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

RefSeq	NP_602297.1
CDS	168..842
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQTSWGRNSFQQHPWQLTQRSDSQELLEEEERSC

Target ORF information:

RefSeq Version	NM_134425.2
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.

Target ORF information:

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

NM_134425.2

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGACGT CCTGGGGTAG AAACAGCTTC 
CAGCAACACC CATGGCAATT AACACAGAGG AGTGACTCGC AGGAACTTCT GGAAGAGGAG 
GAAAGATCTT GCTGA

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

SLC26A1 ( NM_134425.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_602297.1 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu27594
Clone ID Related Accession (Same CDS sequence)	NM_134425.2 , NM_134425.3
Accession Version	NM_134425.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 675bp) 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	2019-08-21
Organism	Homo sapiens(human)
Product	sulfate anion transporter 1 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292747.1 and BC015517.2. This sequence is a reference standard in the RefSeqGene project. On May 31, 2019 this sequence version replaced NM_134425.2. Transcript Variant: This variant (2) lacks an exon in the 5' UTR and has an alternate 3' terminal exon, as compared to variant 3. It encodes isoform b which has a shorter and different C-terminus compared to isoform a. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: BC015517.2, BE787840.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMN04284274 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGACGT CCTGGGGTAG AAACAGCTTC 
CAGCAACACC CATGGCAATT AACACAGAGG AGTGACTCGC AGGAACTTCT GGAAGAGGAG 
GAAAGATCTT GCTGA

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

RefSeq	NP_602297.1
CDS	132..806
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQTSWGRNSFQQHPWQLTQRSDSQELLEEEERSC

Target ORF information:

RefSeq Version	NM_134425.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 2, mRNA.

Target ORF information:

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

NM_134425.3

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGACGT CCTGGGGTAG AAACAGCTTC 
CAGCAACACC CATGGCAATT AACACAGAGG AGTGACTCGC AGGAACTTCT GGAAGAGGAG 
GAAAGATCTT GCTGA

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

SLC26A1 ( NM_213613.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_998778.1 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu27619
Clone ID Related Accession (Same CDS sequence)	NM_213613.3 , NM_022042.3 , NM_213613.4 , NM_022042.4
Accession Version	NM_213613.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 2106bp) 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	sulfate anion transporter 1 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292747.1 and AY124771.1. On Jun 28, 2013 this sequence version replaced NM_213613.2. Transcript Variant: This variant (3) represents the longest transcript and encodes the longer isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AY124771.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA2144835, SAMEA2152474 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

RefSeq	NP_998778.1
CDS	383..2488
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQVLMGVLRLGFVSAYLSQPLLDGFAMGASVTILTSQLKHLLGVRIPRHQGPGMVVLTWLSLLRGAGQANVCDVVTSTVCLAVLLAAKELSDRYRHRLRVPLPTELLVIVVATLVSHFGQLHKRFGSSVAGDIPTGFMPPQVPEPRLMQRVALDAVALALVAAAFSISLAEMFARSHGYSVRANQELLAVGCCNVLPAFLHCFATSAALAKSLVKTATGCRTQLSSVVSATVVLLVLLALAPLFHDLQRSVLACVIVVSLRGALRKVWDLPRLWRMSPADALVWAGTAATCMLVSTEAGLLAGVILSLLSLAGRTQRPRTALLARIGDTAFYEDATEFEGLVPEPGVRVFRFGGPLYYANKDFFLQSLYSLTGLDAGCMAARRKEGGSETGVGEGGPAQGEDLGPVSTRAALVPAAAGFHTVVIDCAPLLFLDAAGVSTLQDLRRDYGALGISLLLACCSPPVRDILSRGGFLGEGPGDTAEEEQLFLSVHDAVQTARARHRELEATDAHL

Target ORF information:

RefSeq Version	NM_213613.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.

Target ORF information:

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

NM_213613.3

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

SLC26A1 ( NM_022042.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_071325.2 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu27619
Clone ID Related Accession (Same CDS sequence)	NM_213613.3 , NM_022042.3 , NM_213613.4 , NM_022042.4
Accession Version	NM_022042.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 2106bp) 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	2017-12-05
Organism	Homo sapiens(human)
Product	sulfate anion transporter 1 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292747.1 and AY124771.1. On Jun 28, 2013 this sequence version replaced NM_022042.2. Transcript Variant: This variant (1) lacks an exon in the 5' UTR, as compared to variant 3. Both variants 1 and 3 encode the same isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AK292747.1, AF297659.2 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2144835 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

RefSeq	NP_071325.2
CDS	168..2273
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQVLMGVLRLGFVSAYLSQPLLDGFAMGASVTILTSQLKHLLGVRIPRHQGPGMVVLTWLSLLRGAGQANVCDVVTSTVCLAVLLAAKELSDRYRHRLRVPLPTELLVIVVATLVSHFGQLHKRFGSSVAGDIPTGFMPPQVPEPRLMQRVALDAVALALVAAAFSISLAEMFARSHGYSVRANQELLAVGCCNVLPAFLHCFATSAALAKSLVKTATGCRTQLSSVVSATVVLLVLLALAPLFHDLQRSVLACVIVVSLRGALRKVWDLPRLWRMSPADALVWAGTAATCMLVSTEAGLLAGVILSLLSLAGRTQRPRTALLARIGDTAFYEDATEFEGLVPEPGVRVFRFGGPLYYANKDFFLQSLYSLTGLDAGCMAARRKEGGSETGVGEGGPAQGEDLGPVSTRAALVPAAAGFHTVVIDCAPLLFLDAAGVSTLQDLRRDYGALGISLLLACCSPPVRDILSRGGFLGEGPGDTAEEEQLFLSVHDAVQTARARHRELEATDAHL

Target ORF information:

RefSeq Version	NM_022042.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.

Target ORF information:

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

NM_022042.3

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

SLC26A1 ( NM_213613.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_998778.1 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu27619
Clone ID Related Accession (Same CDS sequence)	NM_213613.3 , NM_022042.3 , NM_213613.4 , NM_022042.4
Accession Version	NM_213613.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 2106bp) 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	2019-05-30
Organism	Homo sapiens(human)
Product	sulfate anion transporter 1 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AY124771.1. On May 31, 2019 this sequence version replaced NM_213613.3. Transcript Variant: This variant (3) represents the longest transcript and encodes the longer isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AY124771.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA2144835, SAMEA2152474 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

RefSeq	NP_998778.1
CDS	347..2452
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQVLMGVLRLGFVSAYLSQPLLDGFAMGASVTILTSQLKHLLGVRIPRHQGPGMVVLTWLSLLRGAGQANVCDVVTSTVCLAVLLAAKELSDRYRHRLRVPLPTELLVIVVATLVSHFGQLHKRFGSSVAGDIPTGFMPPQVPEPRLMQRVALDAVALALVAAAFSISLAEMFARSHGYSVRANQELLAVGCCNVLPAFLHCFATSAALAKSLVKTATGCRTQLSSVVSATVVLLVLLALAPLFHDLQRSVLACVIVVSLRGALRKVWDLPRLWRMSPADALVWAGTAATCMLVSTEAGLLAGVILSLLSLAGRTQRPRTALLARIGDTAFYEDATEFEGLVPEPGVRVFRFGGPLYYANKDFFLQSLYSLTGLDAGCMAARRKEGGSETGVGEGGPAQGEDLGPVSTRAALVPAAAGFHTVVIDCAPLLFLDAAGVSTLQDLRRDYGALGISLLLACCSPPVRDILSRGGFLGEGPGDTAEEEQLFLSVHDAVQTARARHRELEATDAHL

Target ORF information:

RefSeq Version	NM_213613.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 3, mRNA.

Target ORF information:

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

NM_213613.4

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

SLC26A1 ( NM_022042.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_071325.2 Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu27619
Clone ID Related Accession (Same CDS sequence)	NM_213613.3 , NM_022042.3 , NM_213613.4 , NM_022042.4
Accession Version	NM_022042.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 2106bp) 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	2019-05-01
Organism	Homo sapiens(human)
Product	sulfate anion transporter 1 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK292747.1 and AY124771.1. On Nov 24, 2018 this sequence version replaced NM_022042.3. Transcript Variant: This variant (1) lacks an exon in the 5' UTR, as compared to variant 3. Both variants 1 and 3 encode the same isoform (a). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AF297659.2, AK292747.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1970526, SAMEA2144835 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000398516.3/ ENSP00000381528.2 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

RefSeq	NP_071325.2
CDS	132..2237
Translation	MDESPEPLQQGRGPVPVRRQRPAPRGLREMLKARLWCSCSCSVLCVRALVQDLLPATRWLRQYRPREYLAGDVMSGLVIGIILVPQAIAYSLLAGLQPIYSLYTSFFANLIYFLMGTSRHVSVGIFSLLCLMVGQVVDRELQLAGFDPSQDGLQPGANSSTLNGSAAMLDCGRDCYAIRVATALTLMTGLYQVLMGVLRLGFVSAYLSQPLLDGFAMGASVTILTSQLKHLLGVRIPRHQGPGMVVLTWLSLLRGAGQANVCDVVTSTVCLAVLLAAKELSDRYRHRLRVPLPTELLVIVVATLVSHFGQLHKRFGSSVAGDIPTGFMPPQVPEPRLMQRVALDAVALALVAAAFSISLAEMFARSHGYSVRANQELLAVGCCNVLPAFLHCFATSAALAKSLVKTATGCRTQLSSVVSATVVLLVLLALAPLFHDLQRSVLACVIVVSLRGALRKVWDLPRLWRMSPADALVWAGTAATCMLVSTEAGLLAGVILSLLSLAGRTQRPRTALLARIGDTAFYEDATEFEGLVPEPGVRVFRFGGPLYYANKDFFLQSLYSLTGLDAGCMAARRKEGGSETGVGEGGPAQGEDLGPVSTRAALVPAAAGFHTVVIDCAPLLFLDAAGVSTLQDLRRDYGALGISLLLACCSPPVRDILSRGGFLGEGPGDTAEEEQLFLSVHDAVQTARARHRELEATDAHL

Target ORF information:

RefSeq Version	NM_022042.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 26 member 1 (SLC26A1), transcript variant 1, mRNA.

Target ORF information:

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

NM_022042.4

ORF Insert Sequence:

ATGGACGAGT CCCCTGAGCC TCTGCAGCAG GGCAGAGGGC CGGTGCCGGT CCGACGGCAG 
CGCCCAGCAC CCCGGGGTCT GCGTGAGATG CTGAAGGCCA GGCTGTGGTG CAGCTGCTCG 
TGCAGTGTGC TGTGCGTCCG GGCGCTGGTG CAGGACCTGC TCCCCGCCAC GCGCTGGCTG 
CGTCAGTACC GCCCGCGGGA GTACCTGGCA GGCGACGTCA TGTCTGGGCT GGTCATCGGC 
ATCATCCTGG TGCCGCAGGC CATCGCCTAC TCATTGCTGG CCGGGCTGCA GCCCATCTAC 
AGCCTCTATA CGTCCTTCTT CGCCAACCTC ATCTACTTCC TCATGGGCAC CTCACGGCAT 
GTCTCCGTGG GCATCTTCAG CCTGCTTTGC CTCATGGTGG GGCAGGTGGT GGACCGGGAG 
CTCCAGCTGG CCGGCTTTGA CCCCTCCCAG GACGGCCTGC AGCCCGGAGC CAACAGCAGC 
ACCCTCAACG GCTCGGCTGC CATGCTGGAC TGCGGGCGTG ACTGCTACGC CATCCGTGTC 
GCCACCGCCC TCACGCTGAT GACCGGGCTT TACCAGGTCC TCATGGGCGT CCTCCGGCTG 
GGCTTCGTGT CCGCCTACCT CTCACAGCCA CTGCTCGATG GCTTTGCCAT GGGGGCCTCC 
GTGACCATCC TGACCTCGCA GCTCAAACAC CTGCTGGGCG TGCGGATCCC GCGGCACCAG 
GGGCCCGGCA TGGTGGTCCT CACATGGCTG AGCCTGCTGC GCGGCGCCGG GCAGGCCAAC 
GTGTGCGACG TGGTCACCAG CACGGTGTGC CTGGCGGTGC TGCTAGCCGC GAAGGAGCTC 
TCAGACCGCT ACCGACACCG CCTGAGGGTG CCGCTGCCCA CGGAGCTGCT GGTCATCGTG 
GTGGCCACAC TCGTGTCGCA CTTCGGGCAG CTCCACAAGC GCTTTGGCTC GAGCGTGGCT 
GGCGACATCC CCACGGGTTT CATGCCCCCT CAGGTCCCAG AGCCCAGGCT GATGCAGCGT 
GTGGCTTTGG ATGCCGTGGC CCTGGCCCTC GTGGCTGCCG CCTTCTCCAT CTCGCTGGCG 
GAGATGTTCG CCCGCAGTCA CGGCTACTCT GTGCGTGCCA ACCAGGAGCT GCTGGCTGTG 
GGCTGCTGCA ACGTGCTACC CGCCTTCCTC CACTGCTTCG CCACCAGCGC CGCCCTGGCC 
AAGAGCCTGG TGAAGACAGC CACTGGCTGC CGGACACAGC TGTCCAGCGT GGTCAGCGCC 
ACCGTGGTGC TGCTGGTGCT GCTGGCGCTG GCACCGCTGT TCCACGACCT ACAGCGAAGC 
GTGCTGGCCT GCGTCATCGT GGTCAGCCTG CGGGGGGCCC TGCGCAAGGT GTGGGACCTC 
CCGCGGCTGT GGCGGATGAG CCCGGCTGAC GCGCTGGTCT GGGCAGGCAC CGCGGCCACC 
TGTATGCTGG TCAGCACAGA GGCCGGGCTG CTGGCTGGCG TCATCCTCTC GCTGCTCAGC 
CTGGCCGGCC GCACCCAACG CCCACGCACC GCCCTGCTGG CCCGCATCGG GGACACGGCC 
TTCTACGAGG ATGCCACAGA GTTCGAGGGC CTCGTCCCTG AGCCCGGCGT GCGGGTGTTC 
CGCTTTGGGG GGCCGCTGTA CTATGCCAAC AAGGACTTCT TCCTGCAGTC ACTCTACAGC 
CTCACGGGGC TGGACGCAGG GTGCATGGCT GCCAGGAGGA AGGAGGGGGG CTCAGAGACG 
GGGGTCGGTG AGGGAGGCCC TGCCCAGGGC GAGGACCTGG GCCCGGTTAG CACCAGGGCT 
GCGCTGGTGC CCGCAGCGGC CGGCTTCCAC ACAGTGGTCA TCGACTGCGC CCCGCTGCTG 
TTCCTAGACG CAGCCGGTGT GAGCACGCTG CAGGACCTGC GCCGAGACTA CGGGGCCCTG 
GGCATCAGCC TGCTGCTAGC CTGCTGCAGC CCGCCTGTGA GAGACATTCT GAGCAGAGGA 
GGCTTCCTCG GGGAGGGCCC CGGGGACACG GCTGAGGAGG AGCAGCTGTT CCTCAGTGTG 
CACGATGCCG TGCAGACAGC ACGAGCCCGC CACAGGGAGC TGGAGGCCAC CGATGCCCAT 
CTGTAG

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

PubMed

From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.
G3 (Bethesda, Md.)6(9)2909-18(2016 09)
Tise CG,Perry JA,Anforth LE,Pavlovich MA,Backman JD,Ryan KA,Lewis JP,O'Connell JR,Yerges-Armstrong LM,Shuldiner AR

Extracellular Cl(-) regulates human SO4 (2-)/anion exchanger SLC26A1 by altering pH sensitivity of anion transport.
Pflugers Archiv : European journal of physiology468(8)1311-32(2016 Aug)
Wu M,Heneghan JF,Vandorpe DH,Escobar LI,Wu BL,Alper SL

Mutations in SLC26A1 Cause Nephrolithiasis.
American journal of human genetics98(6)1228-1234(2016 Jun)
Gee HY,Jun I,Braun DA,Lawson JA,Halbritter J,Shril S,Nelson CP,Tan W,Stein D,Wassner AJ,Ferguson MA,Gucev Z,Sayer JA,Milosevic D,Baum M,Tasic V,Lee MG,Hildebrandt F

N-glycosylation and topology of the human SLC26 family of anion transport membrane proteins.
American journal of physiology. Cell physiology306(10)C943-60(2014 May)
Li J,Xia F,Reithmeier RA

Human SLC26A1 gene variants: a pilot study.
TheScientificWorldJournal2013541710(2013)
Dawson PA,Sim P,Mudge DW,Cowley D

- Most Popular Services
  - 人工遺伝子合成& DNA合成-納期保証
- Services & Products

見積依頼

Eメール

japanmarket@genscript.com

電話

03-6811-6572

FAX

03-6811-6573
050-3174-7589(受注専用)

オンラインフォーム

オンライン注文

SLC26A1 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:

Most Popular Services

Services & Products

見積依頼

Eメール

電話

FAX

オンラインフォーム

サポート

会社情報

サポート

会社情報