WNT8B cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	WNT8B
Entrez Gene ID	7479
Full Name	Wnt family member 8B
General protein information	Preferred Names Wnt family member 8B Names protein Wnt-8b wingless-type MMTV integration site family, member 8B
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 10 Map Location: 10q24.31
Summary	The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 95%, 86% and 71% amino acid identity to the mouse, zebrafish and Xenopus Wnt8B proteins, respectively. The expression patterns of the human and mouse genes appear identical and are restricted to the developing brain. The chromosomal location of this gene to 10q24 suggests it as a candidate gene for partial epilepsy. [provided by RefSeq, Jul 2008].
Disorder MIM:	601396

mRNA and Protein(s)

mRNA	Protein	Name
NM_003393.3	NP_003384.2	protein Wnt-8b precursor
NM_003393.4	NP_003384.2	protein Wnt-8b precursor

Pathways from BioSystems

Homologies

Rattus norvegicus (Norway rat)	Wnt8b	NP_001099829.1
Gallus gallus (chicken)	WNT8B	XP_426508.3
Homo sapiens (human)	WNT8B	NP_003384.2
Canis lupus familiaris (dog)	WNT8B	XP_005637677.1
Pan troglodytes (chimpanzee)	WNT8B	XP_521584.2
	WNT8B	XP_001108075.1
Mus musculus (house mouse)	Wnt8b	NP_035850.2
Danio rerio (zebrafish)	wnt8b	NP_571034.1
Xenopus tropicalis (tropical clawed frog)	wnt8b	XP_004915998.1
Bos taurus (cattle)	WNT8B	XP_002698537.2

Gene Ontology
Bibliography

Related articles in PubMed

Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families.
Voloshanenko O, Gmach P, Winter J, Kranz D, Boutros M
FASEB journal : official publication of the Federation of American Societies for Experimental Biology31(11)4832-4844(2017 Nov)

Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Wu JH, Lemaitre RN, Manichaikul A, Guan W, Tanaka T, Foy M, Kabagambe EK, Djousse L, Siscovick D, Fretts AM, Johnson C, King IB, Psaty BM, McKnight B, Rich SS, Chen YD, Nettleton JA, Tang W, Bandinelli S, Jacobs DR Jr, Browning BL, Laurie CC, Gu X, Tsai MY, Steffen LM, Ferrucci L, Fornage M, Mozaffarian D
Circulation. Cardiovascular genetics6(2)171-83(2013 Apr)

[Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease].
Gao H, Zhang ZB, Jiang ZJ, Wang DJ, Huang Y, Wang WL
Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery13(10)758-61(2010 Oct)

Conserved POU/OCT- and GATA-binding sites in 5'-flanking promoter region of mammalian WNT8B orthologs.
Katoh M, Katoh M
International journal of oncology30(5)1273-7(2007 May)

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
Grupe A, Li Y, Rowland C, Nowotny P, Hinrichs AL, Smemo S, Kauwe JS, Maxwell TJ, Cherny S, Doil L, Tacey K, van Luchene R, Myers A, Wavrant-De Vri?ze F, Kaleem M, Hollingworth P, Jehu L, Foy C, Archer N, Hamilton G, Holmans P, Morris CM, Catanese J, Sninsky J, White TJ, Powell J, Hardy J, O'Donovan M, Lovestone S, Jones L, Morris JC, Thal L, Owen M, Williams J, Goate A
American journal of human genetics78(1)78-88(2006 Jan)

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

WNT8b and SHH mutations and abnormal expressions are present in the peripheral blood of children with sporadic Hirschsprung disease.
Title: [Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease].

WNT8B expression in hepatocyte progenitors derived from human ES cells is due to POU5F1 (OCT3/OCT4) and GATA3, and WNT8B expression in diffuse-type gastric cancer is due to POU5F1 and GATA6
Title: Conserved POU/OCT- and GATA-binding sites in 5'-flanking promoter region of mammalian WNT8B orthologs.

Observational study of gene-disease association. (HuGE Navigator)
Title: A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

Expression and regulation of WNT8B mRNA in human tumor cell lines
Title: Expression and regulation of WNT8A and WNT8B mRNAs in human tumor cell lines: up-regulation of WNT8B mRNA by beta-estradiol in MCF-7 cells, and down-regulation of WNT8A and WNT8B mRNAs by retinoic acid in NT2 cells.

significantly up-regulated in gastric cancer cell lines KATO-III (signet-ring cell carcinoma) and MKN45 (poorly differentiated adenocarcinoma), and also in 5 out of 10 cases of primary gastric cancer
Title: Up-regulation of WNT8B mRNA in human gastric cancer.

The following WNT8B gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the WNT8B 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)
OHu17417	NM_003393.4 Latest version!	Homo sapiens Wnt family member 8B (WNT8B), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$202.30 $289.00
View Old Accession Versions >>
OHu17417	NM_003393.3	Homo sapiens Wnt family member 8B (WNT8B), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$202.30 $289.00
Hide Old Accession Versions >>

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** 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)

WNT8B ( NM_003393.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_003384.2 Homo sapiens Wnt family member 8B (WNT8B), mRNA.

Price & Availability↑

CloneID	OHu17417
Clone ID Related Accession (Same CDS sequence)	NM_003393.3 , NM_003393.4
Accession Version	NM_003393.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1056bp) 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	2019-02-16
Organism	Homo sapiens(human)
Product	protein Wnt-8b precursor
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from CN276452.1 and AB073637.1. On Jul 26, 2006 this sequence version replaced NM_003393.2. 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 :: AB073637.1, Y11094.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA2148874 [ECO:0000350] ##Evidence-Data-END##

ATGTTTCTTT CAAAGCCTTC TGTGTACATC TGTCTTTTCA CCTGTGTCCT CCAACTCAGC 
CACAGCTGGT CGGTGAACAA TTTCCTGATG ACTGGTCCAA AGGCTTACCT GATTTACTCC 
AGCAGTGTGG CAGCTGGTGC CCAGAGTGGT ATTGAAGAAT GCAAGTATCA GTTTGCCTGG 
GACCGCTGGA ACTGCCCTGA GAGAGCCCTG CAGCTGTCCA GCCATGGTGG GCTTCGCAGT 
GCCAATCGGG AGACAGCATT TGTGCATGCC ATCAGTTCTG CTGGAGTCAT GTACACCCTG 
ACTAGAAACT GCAGCCTTGG AGATTTTGAT AACTGTGGCT GTGATGACTC CCGCAACGGG 
CAACTGGGGG GACAAGGCTG GCTGTGGGGA GGCTGCAGTG ACAATGTGGG CTTCGGAGAG 
GCGATTTCCA AGCAGTTTGT CGATGCCCTG GAAACAGGAC AGGATGCACG GGCAGCCATG 
AACCTGCACA ACAACGAGGC TGGCCGCAAG GCGGTGAAGG GCACCATGAA ACGCACGTGC 
AAGTGCCACG GCGTGTCTGG CAGCTGCACC ACGCAGACCT GTTGGCTGCA GCTGCCCGAG 
TTCCGCGAGG TGGGCGCGCA CCTGAAGGAG AAGTACCACG CAGCACTCAA GGTGGACCTG 
CTGCAGGGTG CTGGCAACAG CGCGGCCGGC CGCGGCGCCA TCGCCGACAC CTTTCGCTCC 
ATCTCTACCC GGGAGCTGGT GCACCTGGAG GACTCCCCGG ACTACTGCCT GGAGAACAAA 
ACGCTAGGGC TGCTGGGCAC CGAAGGCCGA GAGTGCCTAA GGCGCGGGCG GGCCCTGGGT 
CGCTGGGAAC GCCGCAGCTG CCGCCGGCTC TGCGGGGACT GCGGGCTGGC GGTGGAGGAG 
CGCCGGGCCG AGACCGTGTC CAGCTGCAAC TGCAAGTTCC ACTGGTGCTG CGCAGTCCGC 
TGCGAGCAGT GCCGCCGGAG GGTCACCAAG TACTTCTGTA GCCGCGCAGA GCGGCCGCGG 
GGGGGCGCTG CGCACAAACC CGGGAGAAAA CCCTAA

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

RefSeq	NP_003384.2
CDS	115..1170
Translation	MFLSKPSVYICLFTCVLQLSHSWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP

Target ORF information:

RefSeq Version	NM_003393.3
Organism	Homo sapiens(human)
Definition	Homo sapiens Wnt family member 8B (WNT8B), mRNA.

Target ORF information:

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

NM_003393.3

ORF Insert Sequence:

ATGTTTCTTT CAAAGCCTTC TGTGTACATC TGTCTTTTCA CCTGTGTCCT CCAACTCAGC 
CACAGCTGGT CGGTGAACAA TTTCCTGATG ACTGGTCCAA AGGCTTACCT GATTTACTCC 
AGCAGTGTGG CAGCTGGTGC CCAGAGTGGT ATTGAAGAAT GCAAGTATCA GTTTGCCTGG 
GACCGCTGGA ACTGCCCTGA GAGAGCCCTG CAGCTGTCCA GCCATGGTGG GCTTCGCAGT 
GCCAATCGGG AGACAGCATT TGTGCATGCC ATCAGTTCTG CTGGAGTCAT GTACACCCTG 
ACTAGAAACT GCAGCCTTGG AGATTTTGAT AACTGTGGCT GTGATGACTC CCGCAACGGG 
CAACTGGGGG GACAAGGCTG GCTGTGGGGA GGCTGCAGTG ACAATGTGGG CTTCGGAGAG 
GCGATTTCCA AGCAGTTTGT CGATGCCCTG GAAACAGGAC AGGATGCACG GGCAGCCATG 
AACCTGCACA ACAACGAGGC TGGCCGCAAG GCGGTGAAGG GCACCATGAA ACGCACGTGC 
AAGTGCCACG GCGTGTCTGG CAGCTGCACC ACGCAGACCT GTTGGCTGCA GCTGCCCGAG 
TTCCGCGAGG TGGGCGCGCA CCTGAAGGAG AAGTACCACG CAGCACTCAA GGTGGACCTG 
CTGCAGGGTG CTGGCAACAG CGCGGCCGGC CGCGGCGCCA TCGCCGACAC CTTTCGCTCC 
ATCTCTACCC GGGAGCTGGT GCACCTGGAG GACTCCCCGG ACTACTGCCT GGAGAACAAA 
ACGCTAGGGC TGCTGGGCAC CGAAGGCCGA GAGTGCCTAA GGCGCGGGCG GGCCCTGGGT 
CGCTGGGAAC GCCGCAGCTG CCGCCGGCTC TGCGGGGACT GCGGGCTGGC GGTGGAGGAG 
CGCCGGGCCG AGACCGTGTC CAGCTGCAAC TGCAAGTTCC ACTGGTGCTG CGCAGTCCGC 
TGCGAGCAGT GCCGCCGGAG GGTCACCAAG TACTTCTGTA GCCGCGCAGA GCGGCCGCGG 
GGGGGCGCTG CGCACAAACC CGGGAGAAAA CCCTAA

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

WNT8B ( NM_003393.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_003384.2 Homo sapiens Wnt family member 8B (WNT8B), mRNA.

Price & Availability↑

CloneID	OHu17417
Clone ID Related Accession (Same CDS sequence)	NM_003393.3 , NM_003393.4
Accession Version	NM_003393.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1056bp) 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	2019-10-24
Organism	Homo sapiens(human)
Product	protein Wnt-8b precursor
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AL359759.19, CN276452.1, AB073637.1 and AL133352.12. On May 17, 2019 this sequence version replaced NM_003393.3. 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 :: Y11094.1, GQ891471.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA2148874 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000343737.6/ ENSP00000340677.5 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END##

ATGTTTCTTT CAAAGCCTTC TGTGTACATC TGTCTTTTCA CCTGTGTCCT CCAACTCAGC 
CACAGCTGGT CGGTGAACAA TTTCCTGATG ACTGGTCCAA AGGCTTACCT GATTTACTCC 
AGCAGTGTGG CAGCTGGTGC CCAGAGTGGT ATTGAAGAAT GCAAGTATCA GTTTGCCTGG 
GACCGCTGGA ACTGCCCTGA GAGAGCCCTG CAGCTGTCCA GCCATGGTGG GCTTCGCAGT 
GCCAATCGGG AGACAGCATT TGTGCATGCC ATCAGTTCTG CTGGAGTCAT GTACACCCTG 
ACTAGAAACT GCAGCCTTGG AGATTTTGAT AACTGTGGCT GTGATGACTC CCGCAACGGG 
CAACTGGGGG GACAAGGCTG GCTGTGGGGA GGCTGCAGTG ACAATGTGGG CTTCGGAGAG 
GCGATTTCCA AGCAGTTTGT CGATGCCCTG GAAACAGGAC AGGATGCACG GGCAGCCATG 
AACCTGCACA ACAACGAGGC TGGCCGCAAG GCGGTGAAGG GCACCATGAA ACGCACGTGC 
AAGTGCCACG GCGTGTCTGG CAGCTGCACC ACGCAGACCT GTTGGCTGCA GCTGCCCGAG 
TTCCGCGAGG TGGGCGCGCA CCTGAAGGAG AAGTACCACG CAGCACTCAA GGTGGACCTG 
CTGCAGGGTG CTGGCAACAG CGCGGCCGGC CGCGGCGCCA TCGCCGACAC CTTTCGCTCC 
ATCTCTACCC GGGAGCTGGT GCACCTGGAG GACTCCCCGG ACTACTGCCT GGAGAACAAA 
ACGCTAGGGC TGCTGGGCAC CGAAGGCCGA GAGTGCCTAA GGCGCGGGCG GGCCCTGGGT 
CGCTGGGAAC GCCGCAGCTG CCGCCGGCTC TGCGGGGACT GCGGGCTGGC GGTGGAGGAG 
CGCCGGGCCG AGACCGTGTC CAGCTGCAAC TGCAAGTTCC ACTGGTGCTG CGCAGTCCGC 
TGCGAGCAGT GCCGCCGGAG GGTCACCAAG TACTTCTGTA GCCGCGCAGA GCGGCCGCGG 
GGGGGCGCTG CGCACAAACC CGGGAGAAAA CCCTAA

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

RefSeq	NP_003384.2
CDS	161..1216
Translation	MFLSKPSVYICLFTCVLQLSHSWSVNNFLMTGPKAYLIYSSSVAAGAQSGIEECKYQFAWDRWNCPERALQLSSHGGLRSANRETAFVHAISSAGVMYTLTRNCSLGDFDNCGCDDSRNGQLGGQGWLWGGCSDNVGFGEAISKQFVDALETGQDARAAMNLHNNEAGRKAVKGTMKRTCKCHGVSGSCTTQTCWLQLPEFREVGAHLKEKYHAALKVDLLQGAGNSAAGRGAIADTFRSISTRELVHLEDSPDYCLENKTLGLLGTEGRECLRRGRALGRWERRSCRRLCGDCGLAVEERRAETVSSCNCKFHWCCAVRCEQCRRRVTKYFCSRAERPRGGAAHKPGRKP

Target ORF information:

RefSeq Version	NM_003393.4
Organism	Homo sapiens(human)
Definition	Homo sapiens Wnt family member 8B (WNT8B), mRNA.

Target ORF information:

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

NM_003393.4

ORF Insert Sequence:

ATGTTTCTTT CAAAGCCTTC TGTGTACATC TGTCTTTTCA CCTGTGTCCT CCAACTCAGC 
CACAGCTGGT CGGTGAACAA TTTCCTGATG ACTGGTCCAA AGGCTTACCT GATTTACTCC 
AGCAGTGTGG CAGCTGGTGC CCAGAGTGGT ATTGAAGAAT GCAAGTATCA GTTTGCCTGG 
GACCGCTGGA ACTGCCCTGA GAGAGCCCTG CAGCTGTCCA GCCATGGTGG GCTTCGCAGT 
GCCAATCGGG AGACAGCATT TGTGCATGCC ATCAGTTCTG CTGGAGTCAT GTACACCCTG 
ACTAGAAACT GCAGCCTTGG AGATTTTGAT AACTGTGGCT GTGATGACTC CCGCAACGGG 
CAACTGGGGG GACAAGGCTG GCTGTGGGGA GGCTGCAGTG ACAATGTGGG CTTCGGAGAG 
GCGATTTCCA AGCAGTTTGT CGATGCCCTG GAAACAGGAC AGGATGCACG GGCAGCCATG 
AACCTGCACA ACAACGAGGC TGGCCGCAAG GCGGTGAAGG GCACCATGAA ACGCACGTGC 
AAGTGCCACG GCGTGTCTGG CAGCTGCACC ACGCAGACCT GTTGGCTGCA GCTGCCCGAG 
TTCCGCGAGG TGGGCGCGCA CCTGAAGGAG AAGTACCACG CAGCACTCAA GGTGGACCTG 
CTGCAGGGTG CTGGCAACAG CGCGGCCGGC CGCGGCGCCA TCGCCGACAC CTTTCGCTCC 
ATCTCTACCC GGGAGCTGGT GCACCTGGAG GACTCCCCGG ACTACTGCCT GGAGAACAAA 
ACGCTAGGGC TGCTGGGCAC CGAAGGCCGA GAGTGCCTAA GGCGCGGGCG GGCCCTGGGT 
CGCTGGGAAC GCCGCAGCTG CCGCCGGCTC TGCGGGGACT GCGGGCTGGC GGTGGAGGAG 
CGCCGGGCCG AGACCGTGTC CAGCTGCAAC TGCAAGTTCC ACTGGTGCTG CGCAGTCCGC 
TGCGAGCAGT GCCGCCGGAG GGTCACCAAG TACTTCTGTA GCCGCGCAGA GCGGCCGCGG 
GGGGGCGCTG CGCACAAACC CGGGAGAAAA CCCTAA

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

PubMed

Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology31(11)4832-4844(2017 Nov)
Voloshanenko O,Gmach P,Winter J,Kranz D,Boutros M

Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.
Circulation. Cardiovascular genetics6(2)171-83(2013 Apr)
Wu JH,Lemaitre RN,Manichaikul A,Guan W,Tanaka T,Foy M,Kabagambe EK,Djousse L,Siscovick D,Fretts AM,Johnson C,King IB,Psaty BM,McKnight B,Rich SS,Chen YD,Nettleton JA,Tang W,Bandinelli S,Jacobs DR Jr,Browning BL,Laurie CC,Gu X,Tsai MY,Steffen LM,Ferrucci L,Fornage M,Mozaffarian D

[Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease].
Zhonghua wei chang wai ke za zhi = Chinese journal of gastrointestinal surgery13(10)758-61(2010 Oct)
Gao H,Zhang ZB,Jiang ZJ,Wang DJ,Huang Y,Wang WL

Conserved POU/OCT- and GATA-binding sites in 5'-flanking promoter region of mammalian WNT8B orthologs.
International journal of oncology30(5)1273-7(2007 May)
Katoh M,Katoh M

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
American journal of human genetics78(1)78-88(2006 Jan)
Grupe A,Li Y,Rowland C,Nowotny P,Hinrichs AL,Smemo S,Kauwe JS,Maxwell TJ,Cherny S,Doil L,Tacey K,van Luchene R,Myers A,Wavrant-De Vri?ze F,Kaleem M,Hollingworth P,Jehu L,Foy C,Archer N,Hamilton G,Holmans P,Morris CM,Catanese J,Sninsky J,White TJ,Powell J,Hardy J,O'Donovan M,Lovestone S,Jones L,Morris JC,Thal L,Owen M,Williams J,Goate A

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WNT8B 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:

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