IDUA Antikörper

Produktnummer ABIN7229020

Der Kaninchen Polyklonal anti-IDUA Antikörper (ABIN7229020) detektiert spezifisch IDUA in ELISA und WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human und Maus.

Kurzübersicht für IDUA Antikörper (ABIN7229020)

Target: IDUA (Iduronidase, alpha-L- (IDUA))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser IDUA Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB)

Produktdetails anti-IDUA Antikörper

Verwendungszweck: IDUA Polyclonal Antibody

Spezifität: The antibody detects endogenous levels of IDUA protein

Aufreinigung: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

Immunogen: Synthesized peptide derived from part region of human IDUA protein

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

Kommentare:

Primary Antibody

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Details zu IDUA

Target: IDUA (Iduronidase, alpha-L- (IDUA))

Andere Bezeichnung: IDUA

Hintergrund: Rabbit Anti-IDUA Polyclonal Antibody,Alpha-L-iduronidase,IDUA encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I).,IDUA

Molekulargewicht: observerd band 71kDa

Gen-ID: 3425

UniProt: P35475

Pathways: Glycosaminoglycan Metabolic Process