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SGSH anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-SGSH a été validé pour WB. Il convient pour détecter SGSH dans des échantillons de Humain.
N° du produit ABIN653531

Aperçu rapide pour SGSH anticorps (C-Term) (ABIN653531)

Antigène

Voir toutes SGSH Anticorps
SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))

Reactivité

  • 31
  • 18
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 44
  • 4
  • 1
Lapin

Clonalité

  • 46
  • 3
Polyclonal

Conjugué

  • 25
  • 5
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SGSH est non-conjugé

Application

  • 48
  • 16
  • 13
  • 13
  • 10
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB24406
  • Épitope

    • 15
    • 10
    • 7
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 420-449, C-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This SGSH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 420-449 amino acids from the C-terminal region of human SGSH.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:4000

    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

    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))

    Autre désignation

    SGSH

    Sujet

    SGSH is one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.

    Poids moléculaire

    56695

    ID gène

    6448

    NCBI Accession

    NP_000190

    UniProt

    P51688

    Pathways

    Glycosaminoglycan Metabolic Process
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