AMPD3 Antikörper (AA 280-360)

Produktnummer ABIN8119596

Der Kaninchen Polyklonal anti-AMPD3 Antikörper wird verwendet zum Nachweis von AMPD3 in Proben von Human, Maus und Ratte. Er wurde validiert für IF, IHC und ELISA.

Kurzübersicht für AMPD3 Antikörper (AA 280-360) (ABIN8119596)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AMPD3 Antikörper ist unkonjugiert

Applikation: Immunofluorescence (IF), Immunohistochemistry (IHC), ELISA

Produktdetails anti-AMPD3 Antikörper

Bindungsspezifität: AA 280-360

Verwendungszweck: AMPD3 Antibody

Spezifität: AMPD3 Polyclonal Antibody detects endogenous levels of AMPD3 protein.

Aufreinigung: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from AMPD3 . at AA range: 280-360

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Haltbarkeit: 12 months

Details zu AMPD3

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

Andere Bezeichnung: AMPD3

Hintergrund:

Synonyms: AMPD3, AMP deaminase 3, AMP deaminase isoform E, Erythrocyte AMP deaminase

Background: 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. [provided by RefSeq, Jul 2008],

Gene Name: AMPD3

Protein Name: AMP deaminase 3

Gen-ID: 272

UniProt: Q01432