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Arylsulfatase B anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-Arylsulfatase B a été validé pour WB et IHC (p). Il convient pour détecter Arylsulfatase B dans des échantillons de Humain.
N° du produit ABIN391670

Aperçu rapide pour Arylsulfatase B anticorps (C-Term) (ABIN391670)

Antigène

Voir toutes Arylsulfatase B (ARSB) Anticorps
Arylsulfatase B (ARSB)

Reactivité

  • 35
  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 30
  • 4
  • 1
Lapin

Clonalité

  • 32
  • 3
Polyclonal

Conjugué

  • 18
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Arylsulfatase B est non-conjugé

Application

  • 25
  • 18
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB18353
  • Épitope

    • 7
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 464-493, C-Term

    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.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • 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
  • Antigène

    Arylsulfatase B (ARSB)

    Autre désignation

    ARSB

    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
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