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TBC1D22A anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement TBC1D22A dans ELISA et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN7131302

Aperçu rapide pour TBC1D22A anticorps (ABIN7131302)

Antigène

Voir toutes TBC1D22A Anticorps
TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))

Reactivité

  • 30
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 30
Lapin

Clonalité

  • 30
Polyclonal

Conjugué

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TBC1D22A est non-conjugé

Application

  • 20
  • 13
  • 9
  • 3
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Fonction

    TBC1D22A Antibody

     Réactivité croisée

    Souris

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of Human TBC1D22A

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    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,-80 °C

    Stockage commentaire

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène

    TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))

    Autre désignation

    TBC1D22A

    Sujet

    Background: TBC1D22A (TBC1 domain family, member 22A), also known as C22orf4, is a 517 amino acid protein that contains one Rab-GAP TBC domain and is thought to function as a GTPase-activating protein for Rab family members. Multiple isoforms of TBC1D22A exist due to alternative splicing events. The gene encoding TBC1D22A maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.

    Aliases: TBC1D22A antibody, C22orf4 antibody, TBC1 domain family member 22A antibody

    UniProt

    Q8WUA7
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