WBSCR17 (NM_022479) Human 3' UTR Clone
CAT#: SC214938
3`UTR clone of Williams-Beuren syndrome chromosome region 17 (WBSCR17) for miRNA target validation
Product Images
![](https://cdn.origene.com/img/defaults-img.jpg)
Other products for "WBSCR17"
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 |
Documents
Product Manuals |
FAQs |
SDS |
Resources
{0} Product Review(s)
0 Product Review(s)
Submit review
Be the first one to submit a review
Product Citations
*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.