BBS7 (NM_018190) Human 3' UTR Clone

Specifications

Product Data
Product Name	BBS7 (NM_018190) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BBS2L1
ACCN	NM_018190
Insert Size	444 bp
Sequence Data	Insert Sequence (showhide) >SC205553 3’UTR clone of NM_018190 The sequence shown below is from the reference sequence of NM_018190. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCTGCACATCTTGAAAGACTCTATGGTTAGTGGACCATTCTAGAATACCTTGCCATATTTCTTTTCAAC TGGCTATTTCCCAAGGATCATGTAAGAGAAGCTGGGCAGAAAGATAAAAAGATTACATCAGTCATGATT CATGAACCAGTCATGAATCAGTTGACAACAAATTTATTGCACAGAATATTTCTGTATTTTGTCAAGCTA CTTTTAATATTTAATTCTTTTACTTGATAAAATGCAAGTATATTAAGAAATAAGTATACTGTGATGAAT TAATCTATATATATGAACAAACCTGGTATAAAATGAATGTAATCTATGAACCTTTAGAGCTTAGACTGT ATTTCACACAAATAATTGTCATGTTTTGTTGCTATTGTGAATTATAAAAATGCAGCATTTAAAATTTTT AAGGCAAAATTTAATAAAGGATATACAGTA 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_018190.4
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	17.4

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