LRSAM1 (NM_001005374) Human 3' UTR Clone

Specifications

Product Data
Product Name	LRSAM1 (NM_001005374) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CMT2P; RIFLE; TAL
ACCN	NM_001005374
Insert Size	630 bp
Sequence Data	Insert Sequence (showhide) >SC208325 3’UTR clone of NM_001005374 The sequence shown below is from the reference sequence of NM_001005374. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCGCCTCCGCATCTACCACAGCAGCTGAGTGCTGCCCGCCCACCTGGGCCTGGTCCTAGCCCTGCCT CGGCCACTGTGAGCCCCGGGCTCCTGCTCAGCCTTGTGCCAGCCAGACTCGTATGAGGCTCCCCCCTGC CCTGGGCCCCTTCCCCACTGCCCAGGAGCCCCCATCCTAAGCTCCAAGCATGTCTGGGCCAGGCAGAGG TGCTCCTCATCCATGACACCACCAGTCTGAATGGTCCTGGGGGCTGGGGCTGGAGAGGCCGCTGCACCA CCACCCGAGCCTGGGAGCCAGCGTCCCAGCCTAATCACGGATCTGCTGCCTCCCAGCTGTCTTGACTGA AGGCCACCGCCCCTGCAGGAGCTTGGGTCCTCATCTGGGGGCCATGCACAGGCCCGTCCCACCCTGCAT GTGGGAAGGGAGCAGGAGGGCCTGGCTGGGTGAGGGGAGGCCTTCCTGGGAAGGCGTGTGGTGCAGGCC TGTGCTCACAGTGGCACCAGCAACCCTGGGTCTCCCTCTCTGCTGCTCCCCAGAACCCCGGGGCCCTCC TGCTCTCCACAACTGTCCCTCCTTACCCCATGTAGCTCGATCCGAAGCAGGAGTGTCAATAAACCTGTC TTCAGTGCG 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_001005374.4
Synonyms	CMT2P; RIFLE; TAL
Summary	This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways and cell adhesion, mediation of self-ubiquitylation, and involvement in cargo sorting during receptor endocytosis. Mutations in this gene have been associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jan 2012]
Locus ID	90678
MW	21.7

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