ABCB11 (NM_003742) Human 3' UTR Clone

CAT#: SC208868

3' UTR clone of ATP-binding cassette sub-family B (MDR/TAP) member 11 (ABCB11) for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

Specifications

Product Data
Product Name ABCB11 (NM_003742) Human 3' UTR Clone
Vector pMirTarget
Synonyms ABC16; BRIC2; BSEP; PFIC-2; PFIC2; PGY4; SPGP
ACCN NM_003742
Insert Size 2000 bp
Sequence Data
>SC208868 3’UTR clone of NM_003742
The sequence shown below is from the reference sequence of NM_003742. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CTAGTCACCACTGGATCCCCCATCAGTTGACCCAATGCAAGAATCTCAGACACACATGACGCACCAGTT
ACAGGGGTTGTTTTTAAAGAAAAAAACAATCCCAGCAGGAGGGATTGCTGGGATTGTTTTTTCTTTAAA
GAAGAATGTTAATATTTTACTTTTACAGTCATTTTCCTACATCGGAATCCAAGCTAATTTCTAATGGCC
TTCCATAATAATTCTGCTTTAGATGTGTATACAGAAAATGAAAGAAACTAGGGTCCATATGAGGGAAAA
CCCAATGTCAAGTGGCAGCTCAGCCACCACTCAGTGCTTCTCTGTGCAGGAGCCAGTCCTGATTAATAT
GTGGGAATTAGTGAGACATCAGGGAGTAAGTGACACTTTGAACTCCTCAAGGGCAGAGAACTGTCTTTC
ATTTTTGAACCCTCGGTGTACACAGAGGCGGGTCTATAACAGGCAATCAACAAACGTTTCTTGAGCTAG
ACCAAGGTCAGATTTGAAAAGAACAGAAGGACTGAAGACCAGCTGTGTTTCTTAACTAAATTTGTCTTT
CAAGTGAAACCAGCTTCCTTCATCTCTAAGGCTAAGGATAGGGAAAGGGTGGATGCTCTCAGGCTGAGG
GAGGCAGAAAGGGAAAGTATTAGCATGAGCTTTCCAGTTAGGGCTGTTGATTTATGCTTTAACTTCAGA
GTGAGTGTAGGGGTGGTGATGCTACCATTACTGTGAGGACCTACCAGTGTGGCTGGAGCAGGGACTCTC
TCCCAGGCCTTTTACTCCTCAGCACCTCCCTGCATACTGATTGTTGTTTTTAGTTTCTGTGAAATTATA
TTCATGAAATGAAAATAGCGCATTTTACTTTGCTGTAGTTTCATAAGGTTTTATACAAAAAAGCAAGTA
AATATGGCAGAAAAGCACTCATTTGCCCCTGCTCCCTCAAAACACCACAGAATGACATAGAACTAAAGG
CGGCAGGAATCTACAAGAATGAAGAAAACACAGTGATGCCACCTGCAAAATCTTGGGAGCCAGAAAGCA
AATGGACAATTGATAATAGAGTTACAAGATGAGAGAAAACAAAAATGTAACCTGTTAGTTGGGGGAGCC
TAGAAACATCCTGTTTTGTACCACAGACCCCTAGAAAGTTTCAAGATGTAAAAACACTGGATCCTTCTG
GAAGGAGGAGACAAGGGGACAGAGGGACTGAAGACAGAAGAATGGACCAAAAGCCTGTATGGAAACAGA
ATTGCAGAGCCCCGCCTGCAGCAGGATGGCTGCCTTTCCCCAGTTCCAGCGAGAAACTGCATACTCCCT
CTCTGAGGAGGCTCACAGGGAGGTTTGCACTTAGAGACACAAGATGAAGTTGAAGGGGCAGCTAACATA
CAAGAGACAGGGGGATTGAATGTAAAGCTGTGTATGAACAGAAGAACTCCCAGCCCCTCTCTTCTGGCA
GGAGATTGAAGAATGATTTTCTGGGGAAATTGGCCAATCTTAGAAAAGAGGTCGGGCCAGGCGCTGTGG
CTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCATGAGGTCGAGAGATTGAGACC
ATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGG
GCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTG
CAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAAAAAAAAAAAAAAAGAAAAA
GAAAAAGAAAAGAGGTCAAGGACTCCGTCCTTGGAATCCTAAGAAAATTTTCCAGCCGTATTACCCTTC
TATGAAGCCCACCTGTCAACCAACAAGCACCCACTCGATCAGAGCTTCCCCAGGCTTTTTGGTGTCTCC
TCCTTGCATGGGAATTGACTTCCAAGGACCACCAGACACTGAGGAAGTATTTTAACATATAAAGCAAA
ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA
CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites SgfI-MluI     
OTI Disclaimer Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq NM_003742.4
Synonyms ABC16; BRIC2; BSEP; PFIC-2; PFIC2; PGY4; SPGP
Summary The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is the major canalicular bile salt export pump in man. Mutations in this gene cause a form of progressive familial intrahepatic cholestases which are a group of inherited disorders with severe cholestatic liver disease from early infancy. [provided by RefSeq, Jul 2008]
Locus ID 8647
MW 75.5
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