AMPD3 Antikörper (AA 1-260)

Produktnummer ABIN6136843

Produktdetails anti-AMPD3 Antikörper

Target: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Bindungsspezifität: AA 1-260

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AMPD3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MALSSEPAEM PRQFPKLNIS EVDEQVRLLA EKVFAKVLRE EDSKDALSLF TVPEDCPIGQ KEAKERELQK ELAEQKSVET AKRKKSFKMI RSQSLSLQMP PQQDWKGPPA ASPAMSPTTP VVTGATSLPT PAPYAMPEFQ RVTISGDYCA GITLEDYEQA AKSLAKALMI REKYARLAYH RFPRITSQYL GHPRADTAPP EEGLPDFHPP PLPQEDPYCL DDAPPNLDYL VHMQGGILFV YDNKKMLEHQ EPHSLPYPDL

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human AMPD3 (NP_000471.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

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 AMPD3

Target: AMPD3 (Adenosine Monophosphate Deaminase 3 (AMPD3))

Andere Bezeichnung: AMPD3 (AMPD3 Produkte)

Synonyme: ampd3 antikoerper, fi25h10 antikoerper, wu:fi25h10 antikoerper, zgc:55390 antikoerper, MGC108215 antikoerper, adenosine monophosphate deaminase 3 antikoerper, adenosine monophosphate deaminase 3b antikoerper, AMP deaminase 3 antikoerper, AMPD3 antikoerper, ampd3b antikoerper, PTRG_08116 antikoerper, ampd3 antikoerper, Ampd3 antikoerper

Hintergrund: This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described.,AMPD3,Cardiovascular,Blood,AMPD3

Molekulargewicht: 24 kDa/71 kDa/76 kDa/88 kDa/89 kDa

Gen-ID: 272

UniProt: Q01432