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Anti-IFN gamma Receptor beta/AF-1 Antibody

Anti-IFN gamma Receptor beta/AF-1 Antibody (RMAB-0250737)

Cat. No.: RMAB-0250737

Category: Primary Antibodies

INQUIRY 100 μL Customer Size
Rabbit monoclonal to IFN gamma Receptor beta/AF-1

Product Features

Isotype IgG
Clonality Monoclonal
Host Species Rabbit
Clone Number EPR22171
Form Liquid
Purity Protein A purified
Species Reactivity Human, Recombinant fragment
Immunogen Recombinant fragment.
Applications ELISA, ICC/IF, Flow Cyt
Key Features Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply; Rabbit monoclonal to IFN gamma Receptor beta/AF-1; Suitable for: ELISA, ICC/IF, Flow Cyt; Reacts with: Human, Recombinant fragment

Target Information

Target Symbol IFNGR2
Target Name Interferon gamma receptor 2
UniProt ID P38484
Cellular Localization Membrane.
Function Part of the receptor for interferon gamma. Required for signal transduction. This accessory factor is an integral part of the IFN-gamma signal transduction pathway and is likely to interact with GAF, JAK1, and/or JAK2.
Involvement in Disease Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD); also known as familial disseminated atypical mycobacterial infection. This rare condition confers predisposition to illness caused by moderately virulent mycobacterial species, such as Bacillus Calmette-Guerin (BCG) vaccine and environmental non-tuberculous mycobacteria, and by the more virulent Mycobacterium tuberculosis. Other microorganisms rarely cause severe clinical disease in individuals with susceptibility to mycobacterial infections, with the exception of Salmonella which infects less than 5% of these individuals. The pathogenic mechanism underlying MSMD is the impairment of interferon-gamma mediated immunity, whose severity determines the clinical outcome. Some patients die of overwhelming mycobacterial disease with lepromatous-like lesions in early childhood, whereas others develop, later in life, disseminated but curable infections with tuberculoid granulomas. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance.
Sequence Similarities Belongs to the type II cytokine receptor family. Contains 2 fibronectin type-III domains.

Storage & Shipping

Storage Buffer pH: 7.2; Preservative: 0.01% Sodium azide; Constituents: PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Storage & Shipping Shipped at 4°C. Store at 4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.

For research use only. Not for clinical use.