VAMP1 (NM_016830) Human 3' UTR Clone

Specifications

Product Data
Product Name	VAMP1 (NM_016830) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CMS25; SPAX1; SYB1; VAMP-1
ACCN	NM_016830
Insert Size	625 bp
Sequence Data	Insert Sequence (showhide) >SC208016 3’UTR clone of NM_016830 The sequence shown below is from the reference sequence of NM_016830. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATCGTGGTAGTTATTGTAAGGCGGGACTGAAGAGCTGGAAGAAAGCAGTCAGTACCCTCCCAACGGCCC CCCTCGAAGGTCTCCACTCTCCTCTGGGCTCCTCCTTGCCTAATGCAGGGGGTCACCGCTGGAGAAGAA CCACCACTGTCCTCGATGTGTCCCAAGCCTGGAGCGAATCCGTCCTCTTGGCTCTCCCAGCCCTATCAC AGGAATCATTCCTGGGTTTCTGTCCCTCTGAGGCTCACCAGGTGTAGTTGGCCTTGTTCTTTGGGGGTA TTAGCCCTTCTACTTTCTTTCTCACCCACCCTGTACCCTCTTCTGTGTGTCTCTGCTATCCCCCTTTCC TCCCACCACCCATGTGCATGAGCAAATGTGCAACAAAACCCTGGGACTTTGCAGTCAAATGAAGCTGAG CTTCCCACATCCCGTTCTTCGGTTTGCCATGAGACGATGTGGGGTTTCCACTGTGTGTCTGTCATCACC TCTTTGTCTTTTTTTCCTAACCCTGATCTCATACTTGTATAGAGTAATAACAACAGTTGTACTTCCACC AAAGGCATGTGGCATATTTACCAATGTCATGTATTCTGAACAAAGGCAAAAAATACAAATTCCTACCAT TAAA 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_016830.4
Synonyms	CMS25; SPAX1; SYB1; VAMP-1
Summary	Synapotobrevins, syntaxins, and the synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane. The protein encoded by this gene is a member of the vesicle-associated membrane protein (VAMP)/synaptobrevin family. Mutations in this gene are associated with autosomal dominant spastic ataxia 1. Multiple alternative splice variants have been described, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2014]
Locus ID	6843
MW	22.8

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