PRKAG2 Polyclonal Antibody (E-AB-52889)

For research use only.
Verified Samples |
Verified Samples in IHC: Human esophagus cancer |
Dilution | IHC 1:50-1:300 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Fusion protein of human PRKAG2 |
Abbre | PRKAG2 |
Synonyms | 5''-AMP-activated protein kinase subunit gamma-2, AAKG, AAKG2, AMPK gamma2, AMPK subunit gamma 2, AMPK subunit gamma-2, CMH6, H91620p, Prkag2, Protein kinase AMP activated gamma 2 non catalytic subunit, WPWS |
Swissprot | |
Cellular Localization | Cytosol, Extracellular region or secreted, extracellular space, Nucleus, nucleoplasm, Other locations: nucleotide-activated protein kinase complex. |
Concentration | 0.96 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Antigen affinity purification |
Research Areas | Cardiovascular, Metabolism, Signal Transduction |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
background | AMP-activated protein kinase (AMPK) is a heterotrimeric protein composed of a catalytic alpha subunit, a noncatalytic beta subunit, and a noncatalytic regulatory gamma subunit. Various forms of each of these subunits exist, encoded by different genes. AMPK is an important energy-sensing enzyme that monitors cellular energy status and functions by inactivating key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This gene is a member of the AMPK gamma subunit family. Mutations in this gene have been associated with Wolff-Parkinson-White syndrome, familial hypertrophic cardiomyopathy, and glycogen storage disease of the heart. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. PRKAG2 (Protein Kinase AMP-Activated Non-Catalytic Subunit Gamma 2) is a Protein Coding gene. Diseases associated with PRKAG2 include Glycogen Storage Disease Of Heart, Lethal Congenital and Wolff-Parkinson-White Syndrome. Among its related pathways are RET signaling and Regulation of TP53 Activity. GO annotations related to this gene include protein kinase binding and protein kinase activator activity. An important paralog of this gene is PRKAG1. |
Other Clones
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Other Formats
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Unconjugated
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