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Cat. No.: DPP-001231
| Product Overview | |
|---|---|
| Species | Mouse |
| Expression System | HEK 293 cells |
| Endotoxin Level | < 1.000 Eu/µg |
| Format | Lyophilized |
| Purity | ≥97% by SDS-PAGE |
| Nature | Recombinant |
| Target Information | |
|---|---|
| Gene Name | Ifngr2 |
| UniProt No. | Q63953 |
| Gene ID | 15980 |
| Molecular Weight | 27 kDa including tags |
| Alternative Names | AF 1; AF-1; AF1; IFGR 2; IFGR2; IFN gamma Receptor beta; IFN-gamma receptor 2; IFN-gamma-R2; IFNGR 2; IFNGR2; IFNGT 1; IFNGT1; IMD28; INGR2_HUMAN; Interferon gamma receptor 2; Interferon gamma receptor 2 (interferon gamma transducer 1); Interferon gamma receptor accessory factor 1; Interferon gamma receptor beta chain; Interferon gamma receptor chain 2; Interferon gamma transducer 1 |
| 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 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. |
| Cellular Localization | Membrane. |
| Protein Length | Protein fragment |
| Sequence | MRPLPLWLPS LLLCGLGAAA SSPDSFSQLA APLNPRLHLY NDEQILTWEP SPSSNDPRPV VYQVEYSFI DGSWHRLLEP NCTDITETKC DLTGGGRLKL FPHPFTVFLR VRAKRGNLTS KWVGLEPFQ HYENVTVGPP KNISVTPGKG SLVIHFSPPF DVFHGATFQY LVHYWEKSET QQEQVEGPF KSNSIVLGNL KPYRVYCLQT EAQLILKNKK IRPHGLLSNV SCHETTANAS ARLQQV,Belongs to the type II cytokine receptor family. Contains 2 fibronectin type-III domains. |
| Shipping & Storage | |
|---|---|
| Shipping | Shipped on dry ice. |
| Storage | Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. |
Ace Therapeutics has a team of experts in the field of endocrine and metabolic research, aiming to provide innovative preclinical contract research solutions to cope with diabetes and its complications. We provide customized solutions and technical support, enabling the transformation of promising concepts into innovative treatments, thus accelerating the drug development process of diabetes.
