Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

STK32A anticorps

L’anticorps Lapin Polyclonal anti-STK32A a été validé pour WB, ELISA et IHC. Il convient pour détecter STK32A dans des échantillons de Humain et Souris.
N° du produit ABIN7247471

Aperçu rapide pour STK32A anticorps (ABIN7247471)

Antigène

Voir toutes STK32A Anticorps
STK32A (serine/threonine Kinase 32A (STK32A))

Reactivité

  • 30
  • 23
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 35
  • 3
Lapin

Clonalité

  • 35
  • 3
Polyclonal

Conjugué

  • 21
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp STK32A est non-conjugé

Application

  • 29
  • 20
  • 10
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human STK32A

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, IHC 1:100-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.68 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    STK32A (serine/threonine Kinase 32A (STK32A))

    Autre désignation

    STK32A

    Sujet

    STK32A (serine/threonine kinase 32A), also known as YANK1, is a 396 amino acid protein that belongs to the superfamily of serine/threonine protein kinases and exists as three isoforms. The gene encoding STK32A maps to human chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 46 kDa

    UniProt

    Q8WU08
Vous êtes ici:
Chat with us!