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Anti-IFNGR2 Antibody (clone MMHGR-2) LS-C85249

Catalog Size Price
LS-C85249-250 250 µg (2.5 mg/ml) Unavailable

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37 IFNGR2 Antibodies

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Anti-IFNGR2 Antibody (clone MMHGR-2) LS-C85249
Mouse Monoclonal [clone MMHGR-2] (IgG1) to Human IFNGR2
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Anti-IFNGR2 Antibody (aa308-337) LS-C165132
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IHC, IHC - Paraffin, Western blot, Flow Cytometry
Formalin-fixed and paraffin-embedded human lung carcinoma reacted with IFNGR2 Antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
Anti-IFNGR2 Antibody (aa308-337, FITC) LS-C278430
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Anti-IFNGR2 Antibody (aa308-337) LS-C327638
Rabbit Polyclonal (IgG) to Human IFNGR2
IHC, Western blot, Flow Cytometry, ELISA
Anti-IFNGR2 Antibody LS-C403236
Rabbit Polyclonal (IgG) to Human IFNGR2
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Immunohistochemistry of Human gastric cancer using IFNGR2 Polyclonal Antibody at dilution of 1:40.

100% Guaranteed
Mouse Monoclonal [clone MMHGR-2] (IgG1) to Human IFNGR2
IHC, Immunoprecipitation


Human IFNGR2
Human (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [MMHGR-2]


  • IHC
  • Immunoprecipitation

Specificity and Use

IFNGR2 antibody was raised against human Interferon gamma receptor chain 2.
binds to but does not neutralize human interferon gamma receptor


PBS, 0.1% BSA
+4°C or -20°C, Avoid repeated freezing and thawing.
For research use only.

About IFNGR2

P38484 NM_005534 NP_005525.2

IFNGR2 Antibody, AF-1 Antibody, IFN-gamma receptor 2 Antibody, IFGR2 Antibody, IFNGT1 Antibody, Interferon gamma receptor 2 Antibody, Interferon gamma transducer 1 Antibody, IFN-gamma-R2 Antibody

This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance.

Requested From: 
Date Requested: 4/26/2018

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