Nesprin 1 (SYNE1) (NM_133650) Human 3' UTR Clone

Specifications

Product Data
Product Name	Nesprin 1 (SYNE1) (NM_133650) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	8B; ARCA1; C6orf98; CPG2; dJ45H2.2; DKFZp781J13156; EDMD4; FLJ30878; FLJ41140; KIAA0796
ACCN	NM_133650
Insert Size	779 bp
Sequence Data	Insert Sequence (showhide) >SC209521 3’UTR clone of NM_133650 The sequence shown below is from the reference sequence of NM_133650. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AGATACACGAATGGCCCTCCTCCACTCTGAACTAAGCAGATGCCATCTGCAGAAGTGCTGGTAGCATAA GGAGGATCGGGTCATAAGCAATCCCAAACTACCAACAAGAGGACCTTGATCTTGGCGAAAGCCCTCGGT GTGGCAGCTTTAGCCCTCCTCCAGATCACATGTGTGCAAATTATGGCTTCAGAGGTGGAAGATAAACAG TGACGGGGGAACAAACAGACAACAAGAAGGTTTGGAAGAAATCTGGTTTGAGACTCTGAACCTTAGCAC TAAGGAGATTGAGTAAGGACCTCCAAAGTTCCCCGGACTCATGAATTCTGGGCCCTTGGCCCATTCTGT GCACAGCCAAGGACTTCAGTAGACCATCTGGGCAGCTTTCCCATGGTGCTGCTCCAACCATCAGATAAA TGACCCTCCCAAGCACCATGTCAGTGTCGTACAATCTACCAACCAACCAGTGCTGAAGAGATTTTAGAA CCTTGTAACATACAATTTTTAAGAGCTTATATGGCAGCTTCCTTTTTACCTTGTTTTCCTTTGGGGCAT GATGTTTTAACCTTTGCTTTAGAAGCACAAGCTGTAAATCTAAAAGGCACTTTTTTTTAGAGGTATAAA GAAAAACTAGATGTAATAAATAAGATCATGGAAGGCTTTATGTGAAAAAAGTTGAATGTTATAGTAAAA AAAAAAAGATATTTATGTATGTACAGTTTGCTAAAGCCAAGTTTTGTTTGTATTGATTTCTTTGCATTT ATTATAGATATTATAAAATA 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_133650.2
Synonyms	8B; ARCA1; C6orf98; CPG2; dJ45H2.2; DKFZp781J13156; EDMD4; FLJ30878; FLJ41140; KIAA0796
Summary	This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Locus ID	23345
MW	29.1

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