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Anti-Human PPM1K Polyclonal Antibody (HP361014)

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Overview
Catalog No.HP361014
Species reactivityHuman, Mouse, Rat
ApplicationsELISA, IHC, WB
Host speciesRabbit
ClonalityPolyclonal
IsotypeIgG
Immunogen E. coli - derived recombinant Human PPM1K (Ser91-Ala372).
Target PP2C-type mitochondrial phosphoprotein phosphatase, PP2C-like mitochondrial protein, Protein phosphatase 1K, mitochondrial, PP2CM, PP2C-kappa, PPM1K, PTMP, Protein phosphatase 2C isoform kappa, PP2C domain-containing protein phosphatase 1K
Purification Purified by antigen affinity column.
Accession Q8N3J5
Form Liquid
Storage buffer 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.

Product Usage Information
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stability and Storage Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Background

Protein phosphatase Mn(2+)-dependent 1K (PPM1K) is a ~40 kDa protein. Serine/threonine-protein phosphatase component of macronutrients metabolism. Forms a functional kinase and phosphatase pair with BCKDK, serving as a metabolic regulatory node that coordinates branched-chain amino acids (BCAAs) with glucose and lipid metabolism via two distinct phosphoprotein targets: mitochondrial BCKDHA subunit of the branched-chain alpha-ketoacid dehydrogenase (BCKDH) complex and cytosolic ACLY, a lipogenic enzyme of Krebs cycle. At high levels of branched-chain ketoacids, dephosphorylates and activates mitochondrial BCKDH complex, a multisubunit complex consisting of three multimeric components each involved in different steps of BCAA catabolism: E1 composed of BCKDHA and BCKDHB, E2 core composed of DBT monomers, and E3 composed of DLD monomers. Tightly associates with the E2 component of BCKDH complex and dephosphorylates BCKDHA on Ser-337. Regulates the reversible phosphorylation of ACLY in response to changes in cellular carbohydrate abundance such as occurs during fasting to feeding metabolic transition.

1. Joshi, M. et al. (2007) Biochemical and biophysical research communications 356, 38-44. PMID: 17336929
2. Lu, G. et al. (2007) Genes & development 21, 784-96. PMID: 17374715
3. Lu, G. et al. (2009) The Journal of clinical investigation 119, 1678-87. PMID: 19411760
4. Wynn, RM. et al. (2012) The Journal of biological chemistry 287, 9178-92. PMID: 22291014
5. Zhou, M. et al. (2012) The Journal of biological chemistry 287, 23397-406. PMID: 22589535
6. Oyarzabal, A. et al. (2013) Human mutation 34, 355-62. PMID: 23086801
7. White, PJ. et al. (2018) Cell metabolism 27, 1281-1293.e7. PMID: 29779826
Note For research use only.
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