AMPD1 Antikörper (AA 50-260)

Produktnummer ABIN1678653

Produktdetails anti-AMPD1 Antikörper

Target: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Bindungsspezifität: AA 50-260

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AMPD1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunofluorescence (IF)

Sequenz: AEKVFASEVK DEGGRQEISP FDVDEICPIS HHEMQAHIFH LETLSTSTEA RRKKRFQGRK TVNLSIPLSE TSSTKLSHID EYISSSPTYQ TVPDFQRVQI TGDYASGVTV EDFEIVCKGL YRALCIREKY MQKSFQRFPK TPSKYLRNID GEAWVANESF YPVFTPPVKK GEDPFRTDNL PENLGYHLKM KDGVVYVYPN EAAVSKDEPK P

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 50-260 of human AMPD1 (NP_001166097.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IF,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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 AMPD1

Target: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Andere Bezeichnung: AMPD1 (AMPD1 Produkte)

Synonyme: ampd1 antikoerper, MAD antikoerper, MADA antikoerper, AI553520 antikoerper, Ampd-1 antikoerper, Ampd01 antikoerper, RATAMPD01 antikoerper, zgc:77905 antikoerper, adenosine monophosphate deaminase 1 antikoerper, N-acetyl-anhydromuranmyl-L-alanine amidase antikoerper, N-acetylmuramoyl-L-alanine amidase antikoerper, Negative regulator of beta-lactamase expression antikoerper, adenosine monophosphate deaminase 1 (isoform M) antikoerper, AMPD1 antikoerper, ampD1 antikoerper, ampd1 antikoerper, Ampd1 antikoerper

Hintergrund: Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.,AMPD1,MAD,MADA,MMDD,Cancer,Signal Transduction,Endocrine & Metabolism,AMPD1

Molekulargewicht: 89 kDa/90 kDa

Gen-ID: 270

UniProt: P23109