PYGM Antikörper (C-Term)

Produktnummer ABIN6146527

Produktdetails anti-PYGM Antikörper

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Bindungsspezifität: C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PYGM Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MAEEAGEENF FIFGMRVEDV DKLDQRGYNA QEYYDRIPEL RQVIEQLSSG FFSPKQPDLF KDIVNMLMHH DRFKVFADYE DYIKCQEKVS ALYKNPREWT RMVIRNIATS GKFSSDRTIA QYAREIWGVE PSRQRLPAPD EAI

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: A synthetic peptide corresponding to a sequence within amino acids 700 to the C-terminus of human PYGM (NP_005600.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu PYGM

Target: PYGM (Phosphorylase, Glycogen, Muscle (PYGM))

Andere Bezeichnung: PYGM (PYGM Produkte)

Synonyme: pygb antikoerper, im:7150327 antikoerper, zgc:110706 antikoerper, AI115133 antikoerper, PG antikoerper, Muscpho antikoerper, zgc:63642 antikoerper, phosphorylase, glycogen, muscle L homeolog antikoerper, glycogen phosphorylase, muscle associated antikoerper, phosphorylase, glycogen, muscle A antikoerper, glycogen phosphorylase, muscle form antikoerper, muscle glycogen phosphorylase antikoerper, phosphorylase, glycogen, muscle b antikoerper, pygm.L antikoerper, PYGM antikoerper, pygma antikoerper, THA_70 antikoerper, Pygm antikoerper, pygmb antikoerper

Hintergrund: This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.,PYGM,Cancer,Signal Transduction,Endocrine & Metabolism,Carbohydrate metabolism,Cardiovascular,Hypoxia,Heart,Cardiac metabolism,PYGM

Molekulargewicht: 87 kDa/97 kDa

Gen-ID: 5837

UniProt: P11217

Pathways: Cellular Glucan Metabolic Process