Arylsulfatase B anticorps

N° du produit ABIN2854408

Cet anticorps Lapin Polyclonal détecte spécifiquement Arylsulfatase B dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour Arylsulfatase B anticorps (ABIN2854408)

Antigène: Arylsulfatase B (ARSB)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase B est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Arylsulfatase B anticorps

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Rabbit polyclonal antibody to ARSB (arylsulfatase B)
ARSB antibody [N3C3]

Purification: Affinity purified by Protein A.

Immunogène: Recombinant protein encompassing a sequence within the center region of human ARSB. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: ARSB transfected 293T cell , HeLa , HepG2 , mouse placenta , rat testis

Validation: Overexpression

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 6.11 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur Arylsulfatase B

Antigène: Arylsulfatase B (ARSB)

Autre désignation: arylsulfatase B

Sujet: Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

Cellular Localization: Lysosome

Poids moléculaire: 60 kDa

ID gène: 411

UniProt: P15848

Pathways: Glycosaminoglycan Metabolic Process