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AMPK alpha 2 antibody

GTX103487
GeneTex
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetPRKAA2
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Overview

  • Supplier
    GeneTex
  • Product Name
    AMPK alpha 2 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.96 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID5563
  • Target name
    PRKAA2
  • Target description
    protein kinase AMP-activated catalytic subunit alpha 2
  • Target synonyms
    AMPK, AMPK2, AMPKa2, PRKAA, 5'-AMP-activated protein kinase catalytic subunit alpha-2, 5'-AMP-activated protein kinase, catalytic alpha-2 chain, ACACA kinase, AMPK alpha 2, AMPK subunit alpha-2, AMPK-alpha-2 chain, HMGCR kinase, acetyl-CoA carboxylase kinase, hydroxymethylglutaryl-CoA reductase kinase, protein kinase, AMP-activated, alpha 2 catalytic subunit
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP54646
  • Protein Name
    5'-AMP-activated protein kinase catalytic subunit alpha-2
  • Scientific Description
    The protein encoded by this gene is a catalytic subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. Studies of the mouse counterpart suggest that this catalytic subunit may control whole-body insulin sensitivity and is necessary for maintaining myocardial energy homeostasis during ischemia. [provided by RefSeq]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Gao J, Yuan J, Wang Q, et al. Metformin protects against PM(2.5)-induced lung injury and cardiac dysfunction independent of AMP-activated protein kinase α2. Redox Biol. 2020,28:101345. doi: 10.1016/j.redox.2019.101345
    Read this paper
  • Wang H, Shen X, Tian G, et al. AMPKα2 deficiency exacerbates long-term PM(2.5) exposure-induced lung injury and cardiac dysfunction. Free Radic Biol Med. 2018,121:202-214. doi: 10.1016/j.freeradbiomed.2018.05.008
    Read this paper
  • Wu W, Xu Z, Zhang L, et al. Muscle-specific deletion of Prkaa1 enhances skeletal muscle lipid accumulation in mice fed a high-fat diet. J Physiol Biochem. 2018,74(2):195-205. doi: 10.1007/s13105-017-0604-y
    Read this paper
  • Guo Y, Meng J, Tang Y, et al. AMP-activated kinase α2 deficiency protects mice from denervation-induced skeletal muscle atrophy. Arch Biochem Biophys. 2016,600:56-60. doi: 10.1016/j.abb.2016.04.015
    Read this paper
  • Zhou X, Wu W, Chen J, et al. AMP-activated protein kinase is required for the anti-adipogenic effects of alpha-linolenic acid. Nutr Metab (Lond). 2015,12:10. doi: 10.1186/s12986-015-0006-5
    Read this paper
  • Lee YZ, Yang CW, Chang HY, et al. Discovery of selective inhibitors of Glutaminase-2, which inhibit mTORC1, activate autophagy and inhibit proliferation in cancer cells. Oncotarget. 2014,5(15):6087-101.
    Read this paper
  • Zhou X, Chen J, Wang F, et al. Selenium-enriched exopolysaccharides improve skeletal muscle glucose uptake of diabetic KKAy mice via AMPK pathway. J Physiol Biochem. 2014,70(2):547-54. doi: 10.1007/s13105-014-0334-3
    Read this paper
  • Lin YY, Kiihl S, Suhail Y, et al. Functional dissection of lysine deacetylases reveals that HDAC1 and p300 regulate AMPK. Nature. 2012,482(7384):251-5. doi: 10.1038/nature10804
    Read this paper
  • Hsu YF, Sheu JR, Lin CH, et al. Trichostatin A and sirtinol suppressed survivin expression through AMPK and p38MAPK in HT29 colon cancer cells. Biochim Biophys Acta. 2012,1820(2):104-15. doi: 10.1016/j.bbagen.2011.11.011
    Read this paper