Arylsulfatase B anticorps (C-Term)

N° du produit ABIN391670

Détail du produit anti-Arylsulfatase B anticorps

Antigène: Arylsulfatase B (ARSB)

Épitope: AA 464-493, C-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Arylsulfatase B est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This ARSB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 464-493 amino acids from the C-terminal region of human ARSB.

Clone: RB18353

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Arylsulfatase B

Antigène: Arylsulfatase B (ARSB)

Autre désignation: ARSB (ARSB Produits)

Synonymes: anticorps ASB, anticorps G4S, anticorps MPS6, anticorps 1110007C02Rik, anticorps AI480648, anticorps As-1, anticorps As-1r, anticorps As-1s, anticorps As-1t, anticorps As1, anticorps As1-r, anticorps As1-s, anticorps As1-t, anticorps Asr-1, anticorps Ast-1, anticorps ARSB, anticorps arylsulfatase B, anticorps arylsulfatase, anticorps arylsulfatase b, anticorps ARSB, anticorps Arsb, anticorps RB348, anticorps LOC5566067, anticorps CpipJ_CPIJ011047, anticorps VDBG_03275, anticorps arsb, anticorps LOC5579667

Sujet: ARSB 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.

Poids moléculaire: 59687

ID gène: 411

NCBI Accession: NP_000037, NP_942002

UniProt: P15848

Pathways: Glycosaminoglycan Metabolic Process