Product Name:

DMPK2-NT


Product Number:

ab-nk265-1

Price:

Regular price
$89.00
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Sale price
$89.00

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Target Full Name: Myotonic dystrophy protein kinase 2; Serine-threonine-protein kinase MRCK gamma

Target Alias: MRCKG; Myotonic dystrophy protein kinase like protein ; CDC42BPG; HSMDPKIN

Product Type Specific: Protein kinase pan-specific antibody

Antibody Code: NK265-1

Antibody Target Type: Pan-specific

Protein UniProt: Q6DT37

Protein SigNET: Q6DT37

Antibody Type: Polyclonal

Antibody Host Species: Rabbit

Antibody Immunogen Source: Human DMPK2 (MRCK-g) sequence peptide Cat. No.: PE-01BCS80

Antibody Immunogen Sequence: MERRLRALEQLARGEAGGC

Antibody Immunogen Description: Corresponds to amino acid residues M1 to C19; N-terminus

Production Method: Corresponds to amino acid residues M1 to C19; N-terminus

Antibody Modification: Protein kinase pan-specific antibody

Antibody Concentration: 0.5 mg/ml

Storage Buffer: Phosphate buffered saline pH 7.4, 0.05% Thimerasol

Storage Conditions: For long term storage, keep frozen at -40°C or lower. Stock solution can be kept at +4°C for more than 3 months. Avoid repeated freeze-thaw cycles.

Product Use: Western blotting | Antibody microarray

Antibody Dilution Recommended: 2 µg/ml for immunoblotting

Antibody Species Reactivity: Human

Antibody Positive Control: The observed molecular mass of the processed target protein on SDS-PAGE gels is reported to be around n/a kDa.

Scientific Background: DMPK2 is a protein-serine/threonine kinase of the AGC group and DMPK family. It is a protein kinase that is hypothesized to function as a downstream effector of CDC42 during cytoskeletal rearrangement. Agonist binding to the phorbol ester binding site disrupts this, releasing the kinase domain to allow N-terminus-mediated dimerization and kinase activation by transautophosphorylation. It is maintained in an inactive, closed conformation by an interaction between the kinase domain and the negative autoregulatory C-terminal coiled-coil region. DMPK2 also plays a role in the regulation of actin-myosin contractility through the modulation of MYPT1 and MLC2 activity, which are required for cell invasion and motility. In addition, mutations in the DMPK2 gene have been associated with myotonic dystrophy. The DMPK2 protein is highly expressed in heart and skeletal muscle, with little to no expression in the brain, placenta, lung, liver, kidney, and pancreas. The DMPK2 gene maps to chromosome 11q13.