WBSCR17 (NM_022479) Human 3' UTR Clone

CAT#: SC214938

3`UTR clone of Williams-Beuren syndrome chromosome region 17 (WBSCR17) for miRNA target validation


Reconstitution Protocol

USD 670.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol WBSCR17
Synonyms GalNAc-T5L; GalNAc-T17; GalNAc-T19; GALNACT17; GALNT16; GALNT20; GALNTL3; WBSCR17
ACCN NM_022479
Insert Size 1491
Sequence Data
>SC214938 3'UTR clone of NM_022479
The sequence shown below is from the reference sequence of NM_022479. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

GTCAGAGGTGGACCATTAAGAACTCCATCAAGTAGAGGGAGGGAGCTGGGGCACTGGAGCCTGGCCCCCA
GGACATGGCTGCTCCCCCCAACATCTGGACCAGCTGCCCTGGCGGAGAGACAGCAAGGGGCCGGCAGGTG
CTCGATGGGCCCCCCAGGGCTTCTCCAGGGCAGCACAGGGACCCCGGATGAAGACTCTGTCCCCCCTCAG
GCATTCAGCTGCCCACAAGTTTCCTGCACCCTGGAAAAGCCCCCCACCCTTCCTCTGGGAAACTGACAGC
TGTCTTCCACAGCCTCTGATGTGGACCTGGTACTGAGGAGCAAGACTGTCCAGTTCTCCTCCACATCTCC
CATCCCAGAATCAGGATCTGGGACTGGCAGGGTCCCCTCCTGTGTCTCATCTCTTGCAGCAGCAGCTGCT
GAACTCCAGCCATCAACACGGTGGGAGGCAGCGGGGGCTTCAGCCATGTCCTAGCTCCCCGCCCTAAAAG
GAGGCAGTGAGGACCAGGCACTATTTCCTCCGAGGTTACTTCTACCCAGATGACACCTGCCTGTTCACGC
CCCAAGGCAGCTACTGCCCCTAACCCTTCCCACCAGGGTAGCTTTGGGCACTGCAGCTCTGGACTTTTCT
GGCCCCTCCTGAGATGACCTGATGGAGCTGATGCTTTCTCTCCTAATCCCTGGGCACTAGGCTCTTATCA
GTGTGCTTGGGCCAGCTCTCCTGCCTGTGTCTAGAGGAAGCCAGAGACAGAAATAGGCTAAGCCTGCAGT
AGGATCTCAGCCACAAGGGCCCCGCAGGATGGAGCTGGGTCAAGGACCAGGGAGCCCTGACTCCCAGAGG
CTGCCACCGGGGAGAAGCAGCGGTCCTCCATCCAGAACCTAAGGGCTGAAGCAAAGGCTGCCAGGACCCT
TGAAGATGCTTTTGGCTCACCTCATTTCACCCCACGCTCTGCTGGCTGGCAGAGGAGAAGGCAGTCGTTT
CCTCTCTGAAGAGTATTTTTTTCGATTGCCCTCTGGTTAGGGTGCACATATAAATCAGAGTTAATATATG
AACGCGTGTGCATGCACAAGTGTGTGTGTGCCTGCGTGCTGTGCGTGGCAGGGTGTGTGTGTGTGTGTCT
GGCTGTGCGTTCCGGAGTGTGTGACGATGCTGACCTAGCTGTGTGGCCTTGGGCTTGCTGCTTCATTACT
CACCTGGATGGGGACGAGGGATGAGAAGGGTGTGGGTTTGGCCCCATGTCACTGGCCGGAAGGATGTGTC
TCAGCCCTGCCCTGTGGGGTGCCCCCGATGGGAGGCTGTCCCATCTCCCAGTCCCCATCTCTTTTTCCCC
ACACTGTCCCTGGCCAAGCCCTGCCCAGAGCTGAACCCTGTAGCTGCCCCCTTGCCCTGTGTGGGATTCG
CAGTGTCTCATTTGGTGACGTCTTACTGGTGATCATCTCCTCACCCCATCTCCCACCTTGTGGAATAAAT
ACATGTTAGCACTTCCCAAAA

CGGACCGTTACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
Restriction Sites SgfI-RsrII     
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_022479.1
Summary This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]
Locus ID 64409

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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.