PYGM (NM_005609) Human 3' UTR Clone

Specifications

Product Data
Product Name	PYGM (NM_005609) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GSD5
ACCN	NM_005609
Insert Size	291 bp
Sequence Data	Insert Sequence (showhide) >SC203708 3’UTR clone of NM_005609 The sequence shown below is from the reference sequence of NM_005609. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGCCTGCCAGCCCCGGATGAGGCCATCTGAGCCTCCAGACCAGACCCCAAACCAGCCCTTGAGTCTGTC ACACTCTCTTGGGCCAGCCCCAGCACCTCATGCAGAGGGTGGGGTACTGGAGTTAGATCTCTAAGCCCC TCCTGGAACCCTCATTTTCCCCACTCTCAATGTCCCAGTGTCCAGCGTGACTAAGGACACGGGCCCCCT TCCGTCCTCGGGCTCCCGGTCCCCTCCTATTTATGGGGTCTGACCAACTGCACCCACTCCCTAATAAAT TCATTCTCCTTGGGA 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_005609.4
Synonyms	GSD5
Summary	This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
Locus ID	5837
MW	10.4

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