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IL2RG antibody (APC)

The APC-conjugated Rat Monoclonal anti-IL2RG antibody (Clone TUGh4) (ABIN2658473) specifically detects IL2RG in FACS. The antibody is reactive with Human samples.
Catalog No. ABIN2658473
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Quick Overview for IL2RG antibody (APC) (ABIN2658473)

Target

See all IL2RG Antibodies
IL2RG (Interleukin 2 Receptor, gamma (IL2RG))

Reactivity

  • 81
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  • 26
  • 3
  • 1
Human

Host

  • 58
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Rat

Clonality

  • 60
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Monoclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
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This IL2RG antibody is conjugated to APC

Application

  • 53
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Flow Cytometry (FACS)

Clone

TUGh4
  • Cross-Reactivity

    Dog (Canine)

    Purification

    The antibody was purified by affinity chromatography, and conjugated with APC under optimal conditions. The solution is free of unconjugated APC and unconjugated antibody.

    Isotype

    IgG2b kappa
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Buffer

    Phosphate-buffered solution, pH 7.2, containing 0.09 % sodium azide and 0.2 % (w/v) BSA .

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Protect from prolonged exposure to light. Do not freeze.

    Storage

    4 °C

    Storage Comment

    The antibody solution should be stored undiluted between 2°C and 8°C.
  • Target

    IL2RG (Interleukin 2 Receptor, gamma (IL2RG))

    Alternative Name

    CD132

    Background

    CD132 is a 64-70 kD type I transmembrane glycoprotein of the Ig superfamily, also known as common γ chain (γc), or IL-2 receptor γ subunit. It is expressed broadly on T- and B-lymphocytes, NK cells, monocytes, and granulocytes. CD132 is an essential component of cytokine receptors for IL-2, IL-4, IL-7, IL-9, IL-15 and IL-21. Ligand binding induces tyrosine phosphorylation and initiates signaling through a JAK/STAT pathway. CD132 mutation results in X-linked severe combined immune deficiency (XSCID).

    Pathways

    JAK-STAT Signaling, Growth Factor Binding
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