AMPD3 Antikörper (AA 325-356)

Produktnummer ABIN1538324

Produktdetails anti-AMPD3 Antikörper

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

Bindungsspezifität: AA 325-356

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AMPD3 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This AMPD3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 325-356 amino acids from the Central region of human AMPD3.

Klon: RB17671

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000. WB: 1:1000. WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: Maintain refrigerated at 2-8 deg C for up to 6 months. For long term storage store at -20 deg C in small aliquots to prevent freeze-thaw cycles.

Haltbarkeit: 6 months

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: AMPD3 is a member of the AMP deaminase gene family. This 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. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.

Molekulargewicht: 88812

Gen-ID: 272

NCBI Accession: NP_000471, NP_001020560, NP_001020561, NP_001165901, NP_001165902

UniProt: Q01432