BBS4 (NM_033028) Human 3' UTR Clone

Specifications

Product Data
Product Name	BBS4 (NM_033028) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_033028
Insert Size	916 bp
Sequence Data	Insert Sequence (showhide) >SC210996 3’UTR clone of NM_033028 The sequence shown below is from the reference sequence of NM_033028. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAAACATCAGAACAAATAAGAGAGAAATAAGAATAGAATGAATGACCCCAAAATAGGGTTTTCTTGGGC GAGGATGTGCTGGATTAGGAAAGGTGACATGACACAGGCAGAGCAGAGTGGCACCCACCACAGAATACA GTGTGTGTTATTACGAGGAGCCAGCAGTTGAGCCTAAGGTCCTTCTACCTACCTGGTATTGGCATTTGA GGTCGGAAACCCTCTACTGCCCCATAAGCCAGGAAAAGTGAAAAGAGAACACAGTTCCTTTAAGAACTG GCAGCAAGGCTTGAGGCCTTATGTATGTAGCTGAGTCAGCAAGGTACATGATGCTGTCTGCTTTCAAAA GGACTTTTCTCTCCTAGCTGACTGACTCCTTCCTTAGTTCAAGGAACAGCTGAGACAGACCTCTGCTGA GTAGCTCTGTGATGACAAAGCCTTGGTTTAACTGAGGTGATCCTCAGGTTGTGAGGTTTATTAGTCCCC AAGGCAAACACAAATATTAGATTAATAATCCAACTTTAATAGTATACATTTAAAAGAAAAAAAACAAAA GCCCTGGAAGTTGAGGCCAAGCCTGCTGAGTATTGCAGCTGCATTTGCCCAAAGGGAATCCAGAACAAG TCCCTCCCTGTATTTTGTTCTTGAGAGGGGTCAGTCTAGAAGCTAGATCCTATCAGGATGAGGAGCAGC AGCCCAGGGCTTGTCTGGATCAGCACCAACGATTTTAAAGAAAAAAGGAAGAGTTTCTTAGATGAGTAA TTGTTATTGAAGATAGTCAGTGATAACCACTGACCAGATGCTATCAATACACTATGTGTCCTTTTTAGA ATAAAGATTACATATCATCATTCCTTTGGGGAAAATTGTTATTCAGGTATAAAAACAAGAGATCATAAT AAAAACCTAAAAGAACCTA 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_033028.5
Summary	This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse. The similar phenotypes exhibited by mutations in BBS gene family members are likely due to the protein's shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene has sequence similarity to O-linked N-acetylglucosamine (O-GlcNAc) transferases in plants and archaebacteria and in human forms a multi-protein "BBSome" complex with seven other BBS proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
Locus ID	585
MW	34.4

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