ARG56986

anti-Myosin Light Chain 2 antibody [3B2]

anti-Myosin Light Chain 2 antibody [3B2] for Flow cytometry,Western blot and Human,Rat

Overview

Product Description Mouse Monoclonal antibody [3B2] recognizes Myosin Light Chain 2
Tested Reactivity Hu, Rat
Tested Application FACS, WB
Host Mouse
Clonality Monoclonal
Clone 3B2
Isotype IgG2b, kappa
Target Name Myosin Light Chain 2
Antigen Species Human
Immunogen Recombinant fragment around aa. 1-166 of Human Myosin Light Chain 2.
Conjugation Un-conjugated
Alternate Names MLC2; Myosin regulatory light chain 2, ventricular/cardiac muscle isoform; CMH10; MLC-2; MLC-2v

Application Instructions

Application Suggestion
Tested Application Dilution
FACSAssay-dependent
WB1:1000 - 1:2000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purification with Protein G.
Buffer PBS (pH 7.4), 0.02% Sodium azide and 10% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 10% Glycerol
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 363925 Rat MYL2

GeneID: 4633 Human MYL2

Swiss-port # P08733 Rat Myosin regulatory light chain 2, ventricular/cardiac muscle isoform

Swiss-port # P10916 Human Myosin regulatory light chain 2, ventricular/cardiac muscle isoform

Gene Symbol MYL2
Gene Full Name myosin, light chain 2, regulatory, cardiac, slow
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]
Calculated MW 19 kDa
PTM N-terminus is methylated by METTL11A/NTM1.
Phosphorylated by MYLK3 and MYLK2; promotes cardiac muscle contraction and function (By similarity). Dephosphorylated by PPP1CB complexed to PPP1R12B (By similarity). The phosphorylated form in adult is expressed as gradients across the heart from endocardium (low phosphorylation) to epicardium (high phosphorylation); regulates cardiac torsion and workload distribution (By similarity).