BBS7 (NM_176824) Human 3' UTR Clone
CAT#: SC214364
3' UTR clone of Bardet-Biedl syndrome 7 (BBS7) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | BBS7 (NM_176824) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BBS2L1 |
ACCN | NM_176824 |
Insert Size | 1561 bp |
Sequence Data |
>SC214364 3’UTR clone of NM_176824
The sequence shown below is from the reference sequence of NM_176824. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCATTGATTTCATTCTTCGATGCAGCATGACATACAAATAAGGTAAAGTCCCAAAGAAGTGGTCTGTTT AAATGAAAAATGTTAAAAGAGAATTAGAAGTTAACTGTGTATGTACTTTAATTTCAAATGCTTTTTTAT ATCTAAAAATATTTGAGATATAATGGCTTTTTAAAGTAATGCTTCTATTTCTTTTGACAAATTGAACTT TCTAAAACTAAAAGAGTCTTTTTATTTTTAAAACACAAGTAGAATGATTTAAATAGGATTTTAATGAAT TTTTGGCAAGTGGCTGTTTTAATTTTTAAATTGAGAAGTAATATGTGGAAAATTAAAATATATTCAAAT GTATTACAAGGTACATAAACACATAAACATGTAGACCGCTTTATAGGCTTCAAAATGTATTTTTATATA TTACCTTATTTGATCTTCACAACTGTTGTAAAATTTGTCAAATCATATAAGAAAACTGATTCTCAGTGA AATTTTGTGATTAAGAGGACATGCTAATATTTTGTAAAGCTGGGACCAGAACCCAAGTACTGGTACTTG CTTTGTGTCCTGGTTACTATGTATGTTGCCAGCTAGTGGAAATAACCTACCAATTGTTTTTTCTAGGAG ATAGGATTGATTTGCAACTGATATTCCTTTTGCTTGGTAGTGTTTTATGACTCTGCTGCAGTTTGTGGA AATGCTGGACTTGGCTCAGTGCTATAAATTGTAGCCAGGAAATAAGAAGAGCTTACACAGAGTCGGGGG ATCTTAATTAGACATGCTGTAACCAGTGGAGCTATTCAGCGTGCTTCAAGTGAAGAGTGCAGAAATAGT GATGCCATCTTAGATTTTCCTACACTAGTATCTTCTAGATCTCTTTTTATCATATATGACATTAAGGCT ACAGAAGTTTTGTGCATTAATCTTAATTCATATTTATTAATTTCAAGGGAATATTGAAAGGTTTTAAAA TGGCATACAGATAATGGAAAATAAGCTTTATGTTTCAAGAAGGGCAGACTCACGAATTTTTTAGAAAAC AGTGCTTCTTAATGATATGCTATTATACTTATTAGTTATGTGCAAGCTTTGTATATTCTTATATTTATA TATAAATATAAAAATTTGTTAAAGGCACGTATAGTTAAGAGAGTTTTATTTTAATAAGGTCATATTGTT TTTACTATGTTTAAAAAACTTTACTTCTGAAAGGAACATAATTATATCTAGGTCACTAGAACGTCATTG TGTTTTTTGTTGGTTGCCACAGCTTGGGGAAAAATAGAAAAAAATTAATGACTGTATTTGAATATTTTG TAATGCACTGCTATTTATTATATATATCAACAGTAGTTCAAGGTGCCATCTTAAATTAATTGCATCTTC ATTAGGAAAAATAAAAAGCATAAAACACAATTTCTGGTTACTATGAATAAACGCCTAAATGTTAAGATG ACATTACAGTCTTGACACTTGAGTACTGTATTACTATGTGAGCTCCGTGTTAAATAATTTATGCACATT ATTTAATCCTAACAACCATATGACTGTAGTTATTAGTCCCTAT 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_176824.3 |
Synonyms | BBS2L1 |
Summary | This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy; however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014] |
Locus ID | 55212 |
MW | 61.3 |
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