IDS anticorps

N° du produit ABIN7229018

L’anticorps anti-IDS Polyclonal Lapin est utilisé pour la détection de IDS dans des échantillons de Humain et Souris. Il a été validé pour WB et ELISA.

Aperçu rapide pour IDS anticorps (ABIN7229018)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IDS est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-IDS anticorps

Fonction: Rabbit Anti-IDS Polyclonal Antibody

Specificité: The antibody detects endogenous levels of IDS protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-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 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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.

Date de péremption: 12 months

Détails sur IDS

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

Autre désignation: IDS

Sujet: Iduronate 2-sulfatase, Alpha-L-iduronate sulfate sulfatase, IdursulfaseIDS 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.

Poids moléculaire: 60kD

ID gène: 3423

UniProt: P22304

Pathways: Glycosaminoglycan Metabolic Process