Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
MYL2-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
MYL2-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
MYL2-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
MYL2-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
MYL2-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
Gene Symbol : MYL2
Gene Name : Myosin light chain 2
Chromosome : CHR 12: 110,920,599-110,910,818
Locus : 12q24.11
Alt. Genes : FAM13A
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