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TBC1D22A Antikörper

Dieser Kaninchen Polyklonal Antikörper erkennt spezifisch TBC1D22A in ELISA und IHC. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN7131302

Kurzübersicht für TBC1D22A Antikörper (ABIN7131302)

Target

Alle TBC1D22A Antikörper anzeigen
TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))

Reaktivität

  • 30
  • 5
  • 5
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 30
Kaninchen

Klonalität

  • 30
Polyklonal

Konjugat

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser TBC1D22A Antikörper ist unkonjugiert

Applikation

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

    TBC1D22A Antibody

    Kreuzreaktivität

    Maus

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Fusion protein of Human TBC1D22A

    Isotyp

    IgG
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

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

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

    Andere Bezeichnung

    TBC1D22A

    Hintergrund

    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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