IFN-γRα (phospho Tyr457) rabbit polyclonal, anti-human, mouse, rat, monkey
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EKL-APRab04814
Catalog Number: EKL-APRab04814
Size(s): 50 μl, 100 μl, 500 μl
Isotype: Rabbit IgG
Applications: ELISA,IF,IHC, WB
Datasheet
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Size(s): 50 μl, 100 μl, 500 μl
Isotype: Rabbit IgG
Applications: ELISA,IF,IHC, WB
Datasheet
Request Information
Backgroud: This gene (IFNGR1) encodes the ligand-binding chain (alpha) of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. A genetic variation in IFNGR1 is associated with susceptibility to Helicobacter pylori infection. In addition, defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease, also known as familial disseminated atypical mycobacterial infection. [provided by RefSeq, Jul 2008],disease:Defects in IFNGR1 are a cause of mendelian susceptibility to mycobacterial disease (MSMD) [MIM:209950]; 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 50% 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.,function:Receptor for interferon gamma. Two receptors bind one interferon gamma dimer.,online information:IFNGR1 mutation db,polymorphism:A genetic variation in the IFNGR1 gene is associated with susceptibility to Helicobacter pylori infection [MIM:600263].,PTM:Phosphorylated at Ser/Thr residues.,similarity:Belongs to the type II cytokine receptor family.,similarity:Contains 2 fibronectin type-III domains.,similarity:Contains 2 Ig-like C2-type (immunoglobulin-like) domains.,subunit:Monomer.,
Synonyms: IFNGR1, Interferon gamma receptor 1, IFN-gamma receptor 1, IFN-gamma-R1, CDw119, CD antigen CD119
Gene Name: IFNGR1
Gene ID: 3459
SwissProt ID: P15260
Purification: Affinity purification
Storage: Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.
Synonyms: IFNGR1, Interferon gamma receptor 1, IFN-gamma receptor 1, IFN-gamma-R1, CDw119, CD antigen CD119
Gene Name: IFNGR1
Gene ID: 3459
SwissProt ID: P15260
Purification: Affinity purification
Storage: Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.
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