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TBC1D22A antibody

This Rabbit Polyclonal antibody specifically detects TBC1D22A in ELISA and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN7131302

Quick Overview for TBC1D22A antibody (ABIN7131302)

Target

See all TBC1D22A Antibodies
TBC1D22A (TBC1 Domain Family, Member 22A (TBC1D22A))

Reactivity

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

Host

  • 30
Rabbit

Clonality

  • 30
Polyclonal

Conjugate

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TBC1D22A antibody is un-conjugated

Application

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

    TBC1D22A Antibody

    Cross-Reactivity

    Mouse

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of Human TBC1D22A

    Isotype

    IgG
  • Application Notes

    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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C,-80 °C

    Storage Comment

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

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

    Alternative Name

    TBC1D22A

    Background

    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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