beta Synuclein (SNCB) (NM_003085) Human 3' UTR Clone

Specifications

Product Data
Product Name	beta Synuclein (SNCB) (NM_003085) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_003085
Insert Size	759 bp
Sequence Data	Insert Sequence (showhide) >SC208192 3’UTR clone of NM_003085 The sequence shown below is from the reference sequence of NM_003085. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAATATCAGGAGTATGAGCCAGAGGCGTAGGGGCCCAGGAGAGCCCCCACCAGCAGCACAATTCTGTCC CTGTCCCTGCCCCGCCCCCCAGAGCCAGGGCTGTCCTTAGACTCCTTCTCCCCAATCACGAGATCTTCC TTCCGCTCTGAGGCAACCCCCTCGGAGCCTGTGTTAGTGTCTGTCCATCTGTCTGTCCTACCCGCCCGC GTCCAACCCCGGGGCATGGACAGGGCCAGGGTTGCGGTCGCGGCTGGGAGCCTCGCCCCTCCAGTGTTG CCTCCTCCCATCCAGCGTCTGCGCGGATGTAGCATGTTCTATGTGTTTTTAAACGAAGATCCGAGCGAC GGCTCCTCCCCGATCCCCGACAGTGGCTCTCCAAGCGGCCCCCGGGCAGCCCCAGAGCACCCCGCCCGA CTCCCATTAACCTCGAGAACCTTTTTTTTTTTAACCAAAACCAGGAGCCAGGCTGTGCCATGTCCCCCG CCCCCCATCCCAGCCGGCCCGGTCCGAACGCGGGCGTCGTGTGTTGTGATTGTGGCATGGAGAGTCCCC ATCCCCCCCATGTGAGCGTGTCCCGGGCGGGTGGGCCCGGCCGCCCCCGAGAGTCCATGAATAAAGCTA ATCTGTCTGTAGCCAGAGCCGCACCGGCAGGGCTGGGCTGGGCGCCGGGTGGGGGCGACACGTGGCGGC GAGTCTTCCAGGTCCCAGCCTACCCCTCTGTGCTCTTTGGGGTCTGGCACACACAGCCCAGGTACAAGA 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_003085.5
Summary	This gene encodes a member of a small family of proteins that inhibit phospholipase D2 and may function in neuronal plasticity. The encoded protein is abundant in lesions of patients with Alzheimer disease. A mutation in this gene was found in individuals with dementia with Lewy bodies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Locus ID	6620
MW	26.8

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