SEZ6L2 (NM_001114100) Human 3' UTR Clone

Specifications

Product Data
Product Name	SEZ6L2 (NM_001114100) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	BSRPA; PSK-1
ACCN	NM_001114100
Insert Size	570 bp
Sequence Data	Insert Sequence (showhide) >SC207467 3’UTR clone of NM_001114100 The sequence shown below is from the reference sequence of NM_001114100. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GATACGCGGGAGTATGAAGTTTCCATCTGAACCCCAAGACTACAGCTGCAGGACCCAGGACGCCCCTCC CCTCCTCATTCGGGCAGAGGGAAATACGGGACCCGGTCTCTGCCTCCTGGCTGCCCTCCTCCCTGGCTG TGTAAATAGTCTCCCTATCCCACGAGGGGGCTTTGATGGCCCTGGAGATCCTACAGTAAATAAACCAGC ATCCTGCCGCCCAAAGCCGCCTCTTCTCAGTTGCCAAACGAGGGGCCTGCCCCCCGCCCTACCGGCTTT TGGATTCTGGGAGGGGAACTCTGCCTCCCTGCAAATCTTGCAGCCCCTCCTGCCCAGGGCACCCCTCAA GGACTGCCCCCGATAGCTCTACTGTTCCCTTGGCCACGAAGGTGCCCCCCTCCCAGATGCCCTGGCCCT AGGCCTGACTCCGGCCAGGAGGGTCAGAAGAAGGACAAAGGGGAGAGCTGGGACAAGGCCTTGCCCCCT TCCTGCCATCTCCCCAACCCACAGTCTCTCCACCTTTGCTTCTGAATTCTTGTTTTTGAGCAATAAACA GAAAATCGCCACTTGTAA 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_001114100.3
Synonyms	BSRPA; PSK-1
Summary	This gene encodes a seizure-related protein that is localized on the cell surface. The gene is located in a region of chromosome 16p11.2 that is thought to contain candidate genes for autism spectrum disorders (ASD), though there is no evidence directly implicating this gene in ASD. Increased expression of this gene has been found in lung cancers, and the protein is therefore considered to be a novel prognostic marker for lung cancer. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]
Locus ID	26470
MW	20.8

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