MYL2 rabbit pAb

• Background:

  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]

• Description:

  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],

• UniProt:

  P10916

• Swiss Prot:

  P10916

• Reactivity:

  Human; Mouse; Rat

• Immunogen:

  Synthesized peptide derived from human MYL2. at AA range: 91-140

• Clonality:

  Polyclonal

• Source:

  Rabbit

• Applications:

  WB; ELISA; IHC

• Concentration:

  1 mg/ml

• Dilution:

  WB 1:500-2000; IHC-p 1:50-300; ELISA 2000-20000

• Molecular Weight:

  18kD

• Storage Conditions:

  -20°C/1 year

• Observed Molecular Weight:

  18kD

• Fragment:

  IgG

• Subcellular Location:

  Cytoplasm, myofibril, sarcomere, A band .

• Other Product Names:

  Myosin regulatory light chain 2, ventricular/cardiac muscle isoform (MLC-2) (MLC-2v)

• Gene ID (Human):

  4633