UGT1A5 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	UGT1A5
Entrez Gene ID	54579
Full Name	UDP glucuronosyltransferase family 1 member A5
Synonyms	UDPGT,UDPGT 1-5,UGT1E
General protein information	Preferred Names UDP glucuronosyltransferase family 1 member A5 Names UDP-glucuronosyltransferase 1-5 UDP glucuronosyltransferase 1 family, polypeptide A5 UDP glycosyltransferase 1 family, polypeptide A5 UDP-glucuronosyltransferase 1 family polypeptide A5s UDP-glucuronosyltransferase 1-E UDP-glucuronosyltransferase 1A5 UGT-1E UGT1*5
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 2 Map Location: 2q37.1
Summary	This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. [provided by RefSeq, Jul 2008].
Disorder MIM:	606430

mRNA and Protein(s)

mRNA	Protein	Name
NM_019078.1	NP_061951.1	UDP-glucuronosyltransferase 1-5 precursor

Pathways from BioSystems

Homologies

Homo sapiens (human)	UGT1A5	NP_061951.1
Rattus norvegicus (Norway rat)	Ugt1a3	NP_958827.1

Gene Ontology
Bibliography

Related articles in PubMed

Genome-wide analysis of hepatic lipid content in extreme obesity.
DiStefano JK, Kingsley C, Craig Wood G, Chu X, Argyropoulos G, Still CD, Don? SC, Legendre C, Tembe W, Gerhard GS
Acta diabetologica52(2)373-82(2015 Apr)

An atlas of genetic influences on human blood metabolites.
Shin SY, Fauman EB, Petersen AK, Krumsiek J, Santos R, Huang J, Arnold M, Erte I, Forgetta V, Yang TP, Walter K, Menni C, Chen L, Vasquez L, Valdes AM, Hyde CL, Wang V, Ziemek D, Roberts P, Xi L, Grundberg E, , Waldenberger M, Richards JB, Mohney RP, Milburn MV, John SL, Trimmer J, Theis FJ, Overington JP, Suhre K, Brosnan MJ, Gieger C, Kastenm?ller G, Spector TD, Soranzo N
Nature genetics46(6)543-550(2014 Jun)

Genetic determinants influencing human serum metabolome among African Americans.
Yu B, Zheng Y, Alexander D, Morrison AC, Coresh J, Boerwinkle E
PLoS genetics10(3)e1004212(2014 Mar)

Discovery and refinement of loci associated with lipid levels.
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S, Beckmann JS, Bragg-Gresham JL, Chang HY, Demirkan A, Den Hertog HM, Do R, Donnelly LA, Ehret GB, Esko T, Feitosa MF, Ferreira T, Fischer K, Fontanillas P, Fraser RM, Freitag DF, Gurdasani D, Heikkil? K, Hypp?nen E, Isaacs A, Jackson AU, Johansson ?, Johnson T, Kaakinen M, Kettunen J, Kleber ME, Li X, Luan J, Lyytik?inen LP, Magnusson PKE, Mangino M, Mihailov E, Montasser ME, M?ller-Nurasyid M, Nolte IM, O'Connell JR, Palmer CD, Perola M, Petersen AK, Sanna S, Saxena R, Service SK, Shah S, Shungin D, Sidore C, Song C, Strawbridge RJ, Surakka I, Tanaka T, Teslovich TM, Thorleifsson G, Van den Herik EG, Voight BF, Volcik KA, Waite LL, Wong A, Wu Y, Zhang W, Absher D, Asiki G, Barroso I, Been LF, Bolton JL, Bonnycastle LL, Brambilla P, Burnett MS, Cesana G, Dimitriou M, Doney ASF, D?ring A, Elliott P, Epstein SE, Ingi Eyjolfsson G, Gigante B, Goodarzi MO, Grallert H, Gravito ML, Groves CJ, Hallmans G, Hartikainen AL, Hayward C, Hernandez D, Hicks AA, Holm H, Hung YJ, Illig T, Jones MR, Kaleebu P, Kastelein JJP, Khaw KT, Kim E, Klopp N, Komulainen P, Kumari M, Langenberg C, Lehtim?ki T, Lin SY, Lindstr?m J, Loos RJF, Mach F, McArdle WL, Meisinger C, Mitchell BD, M?ller G, Nagaraja R, Narisu N, Nieminen TVM, Nsubuga RN, Olafsson I, Ong KK, Palotie A, Papamarkou T, Pomilla C, Pouta A, Rader DJ, Reilly MP, Ridker PM, Rivadeneira F, Rudan I, Ruokonen A, Samani N, Scharnagl H, Seeley J, Silander K, Stan??kov? A, Stirrups K, Swift AJ, Tiret L, Uitterlinden AG, van Pelt LJ, Vedantam S, Wainwright N, Wijmenga C, Wild SH, Willemsen G, Wilsgaard T, Wilson JF, Young EH, Zhao JH, Adair LS, Arveiler D, Assimes TL, Bandinelli S, Bennett F, Bochud M, Boehm BO, Boomsma DI, Borecki IB, Bornstein SR, Bovet P, Burnier M, Campbell H, Chakravarti A, Chambers JC, Chen YI, Collins FS, Cooper RS, Danesh J, Dedoussis G, de Faire U, Feranil AB, Ferri?res J, Ferrucci L, Freimer NB, Gieger C, Groop LC, Gudnason V, Gyllensten U, Hamsten A, Harris TB, Hingorani A, Hirschhorn JN, Hofman A, Hovingh GK, Hsiung CA, Humphries SE, Hunt SC, Hveem K, Iribarren C, J?rvelin MR, Jula A, K?h?nen M, Kaprio J, Kes?niemi A, Kivimaki M, Kooner JS, Koudstaal PJ, Krauss RM, Kuh D, Kuusisto J, Kyvik KO, Laakso M, Lakka TA, Lind L, Lindgren CM, Martin NG, M?rz W, McCarthy MI, McKenzie CA, Meneton P, Metspalu A, Moilanen L, Morris AD, Munroe PB, Nj?lstad I, Pedersen NL, Power C, Pramstaller PP, Price JF, Psaty BM, Quertermous T, Rauramaa R, Saleheen D, Salomaa V, Sanghera DK, Saramies J, Schwarz PEH, Sheu WH, Shuldiner AR, Siegbahn A, Spector TD, Stefansson K, Strachan DP, Tayo BO, Tremoli E, Tuomilehto J, Uusitupa M, van Duijn CM, Vollenweider P, Wallentin L, Wareham NJ, Whitfield JB, Wolffenbuttel BHR, Ordovas JM, Boerwinkle E, Palmer CNA, Thorsteinsdottir U, Chasman DI, Rotter JI, Franks PW, Ripatti S, Cupples LA, Sandhu MS, Rich SS, Boehnke M, Deloukas P, Kathiresan S, Mohlke KL, Ingelsson E, Abecasis GR,
Nature genetics45(11)1274-1283(2013 Nov)

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

Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
Title: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Observational study of gene-disease association. (HuGE Navigator)
Title: Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy.

Observational study of gene-disease association. (HuGE Navigator)
Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

Observational study of genotype prevalence. (HuGE Navigator)
Title: Genetic variations and haplotypes of UDP-glucuronosyltransferase 1A locus in a Korean population.

The following UGT1A5 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the UGT1A5 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)	Select
OHu24854	NM_019078.1 Latest version!	Homo sapiens UDP glucuronosyltransferase family 1 member A5 (UGT1A5), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$307.30 $439.00

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)

UGT1A5 ( NM_019078.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_061951.1 Homo sapiens UDP glucuronosyltransferase family 1 member A5 (UGT1A5), mRNA.

Price & Availability↑

CloneID	OHu24854
Clone ID Related Accession (Same CDS sequence)	NM_019078.1
Accession Version	NM_019078.1 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1605bp) 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	2019-05-03
Organism	Homo sapiens(human)
Product	UDP-glucuronosyltransferase 1-5 precursor
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AY435140.1. This sequence is a reference standard in the RefSeqGene project. 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 :: AY435140.1 [ECO:0000332] ##Evidence-Data-END## ##RefSeq-Attributes-START## RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGCCACAG GACTCCAGGT TCCCCTGCCG CAGCTGGCCA CAGGACTGCT GCTTCTCCTC 
AGTGTCCAGC CCTGGGCTGA GAGTGGGAAG GTGCTGGTGG TGCCCACTGA TGGCAGCCAC 
TGGCTCAGCA TGCGGGAGGC CTTGCGGGAC CTCCATGCGA GAGGCCACCA GGTGGTGGTC 
CTCACCCTGG AGGTGAATAT GTACATCAAA GAAGAGAACT TTTTCACCCT GACAACGTAT 
GCCATTTCAT GGACCCAGGA CGAATTTGAT CGCCTTTTGC TGGGTCACAC TCAATCGTTC 
TTTGAAACAG AACATCTTCT GATGAAATTT TCTAGAAGAA TGGCAATTAT GAACAATATG 
TCTTTGATCA TACATAGGTC TTGTGTGGAG CTACTGCATA ATGAGGCCCT GATCAGGCAC 
CTGCATGCTA CTTCCTTTGA TGTGGTTCTA ACAGACCCCT TTCACCTCTG CGCGGCGGTG 
CTGGCTAAGT ACCTGTCGAT TCCTGCTGTG TTTTTCTTGA GGAACATTCC ATGTGATTTA 
GACTTTAAGG GCACACAGTG TCCAAACCCT TCCTCCTATA TTCCTAGATT ACTAACGACC 
AATTCAGACC ACATGACATT CCTGCAAAGG GTCAAGAACA TGCTCTACCC TCTGGCCCTG 
TCCTACCTTT GCCATGCTGT TTCTGCTCCT TATGCAAGCC TTGCCTCTGA GCTTTTTCAG 
AGAGAGGTGT CAGTGGTGGA TCTTGTCAGC CATGCATCTG TGTGGCTGTT CCGAGGGGAC 
TTTGTGATGG ATTACCCCAG GCCGATCATG CCCAACATGG TCTTCATTGG GGGCATCAAC 
TGTGCCAACG GGAAGCCACT ATCTCAGGAA TTTGAAGCCT ACATTAATGC TTCTGGAGAA 
CATGGAATTG TGGTTTTCTC TTTGGGATCA ATGGTCTCAG AAATTCCAGA GAAGAAAGCT 
ATGGCAATTG CTGATGCTTT GGGCAAAATC CCTCAGACAG TCCTGTGGCG GTACACTGGA 
ACCCGACCAT CGAATCTTGC GAACAACACG ATACTTGTTA AGTGGCTACC CCAAAACGAT 
CTGCTTGGTC ACCCGATGAC CCGTGCCTTT ATCACCCATG CTGGTTCCCA TGGTGTTTAT 
GAAAGCATAT GCAATGGCGT TCCCATGGTG ATGATGCCCT TGTTTGGTGA TCAGATGGAC 
AATGCAAAGC GCATGGAGAC TAAGGGAGCT GGAGTGACCC TGAATGTTCT GGAAATGACT 
TCTGAAGATT TAGAAAATGC TCTAAAAGCA GTCATCAATG ACAAAAGTTA CAAGGAGAAC 
ATCATGCGCC TCTCCAGCCT TCACAAGGAC CGCCCGGTGG AGCCGCTGGA CCTGGCCGTG 
TTCTGGGTGG AGTTTGTGAT GAGGCACAAG GGCGCGCCAC ACCTGCGCCC CGCAGCCCAC 
GACCTCACCT GGTACCAGTA CCATTCCTTG GACGTGATTG GTTTCCTCTT GGCCGTCGTG 
CTGACAGTGG CCTTCATCAC CTTTAAATGT TGTGCTTATG GCTACCGGAA ATGCTTGGGG 
AAAAAAGGGC GAGTTAAGAA AGCCCACAAA TCCAAGACCC ATTGA

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

RefSeq	NP_061951.1
CDS	1..1605
Translation	MATGLQVPLPQLATGLLLLLSVQPWAESGKVLVVPTDGSHWLSMREALRDLHARGHQVVVLTLEVNMYIKEENFFTLTTYAISWTQDEFDRLLLGHTQSFFETEHLLMKFSRRMAIMNNMSLIIHRSCVELLHNEALIRHLHATSFDVVLTDPFHLCAAVLAKYLSIPAVFFLRNIPCDLDFKGTQCPNPSSYIPRLLTTNSDHMTFLQRVKNMLYPLALSYLCHAVSAPYASLASELFQREVSVVDLVSHASVWLFRGDFVMDYPRPIMPNMVFIGGINCANGKPLSQEFEAYINASGEHGIVVFSLGSMVSEIPEKKAMAIADALGKIPQTVLWRYTGTRPSNLANNTILVKWLPQNDLLGHPMTRAFITHAGSHGVYESICNGVPMVMMPLFGDQMDNAKRMETKGAGVTLNVLEMTSEDLENALKAVINDKSYKENIMRLSSLHKDRPVEPLDLAVFWVEFVMRHKGAPHLRPAAHDLTWYQYHSLDVIGFLLAVVLTVAFITFKCCAYGYRKCLGKKGRVKKAHKSKTH

Target ORF information:

RefSeq Version	NM_019078.1
Organism	Homo sapiens(human)
Definition	Homo sapiens UDP glucuronosyltransferase family 1 member A5 (UGT1A5), mRNA.

Target ORF information:

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

NM_019078.1

ORF Insert Sequence:

ATGGCCACAG GACTCCAGGT TCCCCTGCCG CAGCTGGCCA CAGGACTGCT GCTTCTCCTC 
AGTGTCCAGC CCTGGGCTGA GAGTGGGAAG GTGCTGGTGG TGCCCACTGA TGGCAGCCAC 
TGGCTCAGCA TGCGGGAGGC CTTGCGGGAC CTCCATGCGA GAGGCCACCA GGTGGTGGTC 
CTCACCCTGG AGGTGAATAT GTACATCAAA GAAGAGAACT TTTTCACCCT GACAACGTAT 
GCCATTTCAT GGACCCAGGA CGAATTTGAT CGCCTTTTGC TGGGTCACAC TCAATCGTTC 
TTTGAAACAG AACATCTTCT GATGAAATTT TCTAGAAGAA TGGCAATTAT GAACAATATG 
TCTTTGATCA TACATAGGTC TTGTGTGGAG CTACTGCATA ATGAGGCCCT GATCAGGCAC 
CTGCATGCTA CTTCCTTTGA TGTGGTTCTA ACAGACCCCT TTCACCTCTG CGCGGCGGTG 
CTGGCTAAGT ACCTGTCGAT TCCTGCTGTG TTTTTCTTGA GGAACATTCC ATGTGATTTA 
GACTTTAAGG GCACACAGTG TCCAAACCCT TCCTCCTATA TTCCTAGATT ACTAACGACC 
AATTCAGACC ACATGACATT CCTGCAAAGG GTCAAGAACA TGCTCTACCC TCTGGCCCTG 
TCCTACCTTT GCCATGCTGT TTCTGCTCCT TATGCAAGCC TTGCCTCTGA GCTTTTTCAG 
AGAGAGGTGT CAGTGGTGGA TCTTGTCAGC CATGCATCTG TGTGGCTGTT CCGAGGGGAC 
TTTGTGATGG ATTACCCCAG GCCGATCATG CCCAACATGG TCTTCATTGG GGGCATCAAC 
TGTGCCAACG GGAAGCCACT ATCTCAGGAA TTTGAAGCCT ACATTAATGC TTCTGGAGAA 
CATGGAATTG TGGTTTTCTC TTTGGGATCA ATGGTCTCAG AAATTCCAGA GAAGAAAGCT 
ATGGCAATTG CTGATGCTTT GGGCAAAATC CCTCAGACAG TCCTGTGGCG GTACACTGGA 
ACCCGACCAT CGAATCTTGC GAACAACACG ATACTTGTTA AGTGGCTACC CCAAAACGAT 
CTGCTTGGTC ACCCGATGAC CCGTGCCTTT ATCACCCATG CTGGTTCCCA TGGTGTTTAT 
GAAAGCATAT GCAATGGCGT TCCCATGGTG ATGATGCCCT TGTTTGGTGA TCAGATGGAC 
AATGCAAAGC GCATGGAGAC TAAGGGAGCT GGAGTGACCC TGAATGTTCT GGAAATGACT 
TCTGAAGATT TAGAAAATGC TCTAAAAGCA GTCATCAATG ACAAAAGTTA CAAGGAGAAC 
ATCATGCGCC TCTCCAGCCT TCACAAGGAC CGCCCGGTGG AGCCGCTGGA CCTGGCCGTG 
TTCTGGGTGG AGTTTGTGAT GAGGCACAAG GGCGCGCCAC ACCTGCGCCC CGCAGCCCAC 
GACCTCACCT GGTACCAGTA CCATTCCTTG GACGTGATTG GTTTCCTCTT GGCCGTCGTG 
CTGACAGTGG CCTTCATCAC CTTTAAATGT TGTGCTTATG GCTACCGGAA ATGCTTGGGG 
AAAAAAGGGC GAGTTAAGAA AGCCCACAAA TCCAAGACCC ATTGA

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

PubMed

Genome-wide analysis of hepatic lipid content in extreme obesity.
Acta diabetologica52(2)373-82(2015 Apr)
DiStefano JK,Kingsley C,Craig Wood G,Chu X,Argyropoulos G,Still CD,Don? SC,Legendre C,Tembe W,Gerhard GS

An atlas of genetic influences on human blood metabolites.
Nature genetics46(6)543-550(2014 Jun)
Shin SY,Fauman EB,Petersen AK,Krumsiek J,Santos R,Huang J,Arnold M,Erte I,Forgetta V,Yang TP,Walter K,Menni C,Chen L,Vasquez L,Valdes AM,Hyde CL,Wang V,Ziemek D,Roberts P,Xi L,Grundberg E,,Waldenberger M,Richards JB,Mohney RP,Milburn MV,John SL,Trimmer J,Theis FJ,Overington JP,Suhre K,Brosnan MJ,Gieger C,Kastenm?ller G,Spector TD,Soranzo N

Genetic determinants influencing human serum metabolome among African Americans.
PLoS genetics10(3)e1004212(2014 Mar)
Yu B,Zheng Y,Alexander D,Morrison AC,Coresh J,Boerwinkle E

Discovery and refinement of loci associated with lipid levels.
Nature genetics45(11)1274-1283(2013 Nov)
Willer CJ,Schmidt EM,Sengupta S,Peloso GM,Gustafsson S,Kanoni S,Ganna A,Chen J,Buchkovich ML,Mora S,Beckmann JS,Bragg-Gresham JL,Chang HY,Demirkan A,Den Hertog HM,Do R,Donnelly LA,Ehret GB,Esko T,Feitosa MF,Ferreira T,Fischer K,Fontanillas P,Fraser RM,Freitag DF,Gurdasani D,Heikkil? K,Hypp?nen E,Isaacs A,Jackson AU,Johansson ?,Johnson T,Kaakinen M,Kettunen J,Kleber ME,Li X,Luan J,Lyytik?inen LP,Magnusson PKE,Mangino M,Mihailov E,Montasser ME,M?ller-Nurasyid M,Nolte IM,O'Connell JR,Palmer CD,Perola M,Petersen AK,Sanna S,Saxena R,Service SK,Shah S,Shungin D,Sidore C,Song C,Strawbridge RJ,Surakka I,Tanaka T,Teslovich TM,Thorleifsson G,Van den Herik EG,Voight BF,Volcik KA,Waite LL,Wong A,Wu Y,Zhang W,Absher D,Asiki G,Barroso I,Been LF,Bolton JL,Bonnycastle LL,Brambilla P,Burnett MS,Cesana G,Dimitriou M,Doney ASF,D?ring A,Elliott P,Epstein SE,Ingi Eyjolfsson G,Gigante B,Goodarzi MO,Grallert H,Gravito ML,Groves CJ,Hallmans G,Hartikainen AL,Hayward C,Hernandez D,Hicks AA,Holm H,Hung YJ,Illig T,Jones MR,Kaleebu P,Kastelein JJP,Khaw KT,Kim E,Klopp N,Komulainen P,Kumari M,Langenberg C,Lehtim?ki T,Lin SY,Lindstr?m J,Loos RJF,Mach F,McArdle WL,Meisinger C,Mitchell BD,M?ller G,Nagaraja R,Narisu N,Nieminen TVM,Nsubuga RN,Olafsson I,Ong KK,Palotie A,Papamarkou T,Pomilla C,Pouta A,Rader DJ,Reilly MP,Ridker PM,Rivadeneira F,Rudan I,Ruokonen A,Samani N,Scharnagl H,Seeley J,Silander K,Stan??kov? A,Stirrups K,Swift AJ,Tiret L,Uitterlinden AG,van Pelt LJ,Vedantam S,Wainwright N,Wijmenga C,Wild SH,Willemsen G,Wilsgaard T,Wilson JF,Young EH,Zhao JH,Adair LS,Arveiler D,Assimes TL,Bandinelli S,Bennett F,Bochud M,Boehm BO,Boomsma DI,Borecki IB,Bornstein SR,Bovet P,Burnier M,Campbell H,Chakravarti A,Chambers JC,Chen YI,Collins FS,Cooper RS,Danesh J,Dedoussis G,de Faire U,Feranil AB,Ferri?res J,Ferrucci L,Freimer NB,Gieger C,Groop LC,Gudnason V,Gyllensten U,Hamsten A,Harris TB,Hingorani A,Hirschhorn JN,Hofman A,Hovingh GK,Hsiung CA,Humphries SE,Hunt SC,Hveem K,Iribarren C,J?rvelin MR,Jula A,K?h?nen M,Kaprio J,Kes?niemi A,Kivimaki M,Kooner JS,Koudstaal PJ,Krauss RM,Kuh D,Kuusisto J,Kyvik KO,Laakso M,Lakka TA,Lind L,Lindgren CM,Martin NG,M?rz W,McCarthy MI,McKenzie CA,Meneton P,Metspalu A,Moilanen L,Morris AD,Munroe PB,Nj?lstad I,Pedersen NL,Power C,Pramstaller PP,Price JF,Psaty BM,Quertermous T,Rauramaa R,Saleheen D,Salomaa V,Sanghera DK,Saramies J,Schwarz PEH,Sheu WH,Shuldiner AR,Siegbahn A,Spector TD,Stefansson K,Strachan DP,Tayo BO,Tremoli E,Tuomilehto J,Uusitupa M,van Duijn CM,Vollenweider P,Wallentin L,Wareham NJ,Whitfield JB,Wolffenbuttel BHR,Ordovas JM,Boerwinkle E,Palmer CNA,Thorsteinsdottir U,Chasman DI,Rotter JI,Franks PW,Ripatti S,Cupples LA,Sandhu MS,Rich SS,Boehnke M,Deloukas P,Kathiresan S,Mohlke KL,Ingelsson E,Abecasis GR,

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

UGT1A5 cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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