IDS anticorps

N° du produit ABIN7229018

L’anticorps Lapin Polyclonal anti-IDS a été validé pour WB et ELISA. Il convient pour détecter IDS dans des échantillons de Humain.

Aperçu rapide pour IDS anticorps (ABIN7229018)

Antigène: IDS (Iduronate 2-Sulfatase (IDS))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IDS est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-IDS anticorps

Fonction: IDS Polyclonal Antibody

Specificité: The antibody detects endogenous levels of IDS protein

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

Immunogène: Synthesized peptide derived from part region of human IDS protein

Isotype: IgG

Information d'application

Indications d'application: 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).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur IDS

Antigène: IDS (Iduronate 2-Sulfatase (IDS))

Autre désignation: IDS

Sujet: Rabbit Anti-IDS Polyclonal Antibody,Iduronate 2-sulfatase, Alpha-L-iduronate sulfate sulfatase, Idursulfase,IDS encodes a member of the sulfatase family of proteins. Iduronate 2-Sulfatase is proteolytically processed to generate two polypeptide chains. This enzyme is involved in the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II, also known as Hunter syndrome. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.,IDS

Poids moléculaire: observerd band 60kDa

ID gène: 3423

UniProt: P22304

Pathways: Glycosaminoglycan Metabolic Process