Myotilin (MYOT) (NM_001135940) Human 3' UTR Clone

Specifications

Product Data
Product Name	Myotilin (MYOT) (NM_001135940) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LGMD1; LGMD1A; MFM3; TTID; TTOD
ACCN	NM_001135940
Insert Size	496 bp
Sequence Data	Insert Sequence (showhide) >SC206542 3’UTR clone of NM_001135940 The sequence shown below is from the reference sequence of NM_001135940. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCTGGACTCTATGAAAGTGAAGAACTTTAATAACTTTACCAACATTGGAAAACAGCCAACTACACCATT AGTAATATATTTGATTACATTTTTTTGAAATTAATCCATAGCTGTATTAACAGATTATGGTTTTAATTA GGTAATATAGTTAATATATATTTATAATATTATTTATCCTTTGACTCTTGCACATTCTATGTACCCCTC CGATTTGTGAAGCCTACAGGAAATCTGGGTATATGGATTTGTAACTGCAGAAGACTATCTTAAAATACA GGATTTTAACATTTAAGTCATGCACATTTAACAATTACAGGTTATAAATTAGTATCAACTTTTTAAACA CATCTAATGCTTGTAATAACGTTTACTGGTACTGCTTTCTAAATACTGTTTTACCCGTTTTCTCTTGTA GGAATACTAACATGGTATAGATTATCTGAGTGTTCCACAGTTGTATGTCAAAAGAAAATAAAATTCAAA TATTTAAAACGGA 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_001135940.2
Synonyms	LGMD1; LGMD1A; MFM3; TTID; TTOD
Summary	This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.[provided by RefSeq, Oct 2008]
Locus ID	9499
MW	19.5

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