1-832-868-1888
order@swbio.com
Catalog Number: |
58015 |
other_names: | |
Amount: |
100μg/100μ |
calculated_mw: | |
host_species: | |
Price: |
$390 |
Swiss-Prot No: |
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Form of Antibody: |
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl,0.02% sodium azide and 50% glycerol. |
Storage/Stability: |
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Immunogen: |
synthetic phosphopeptide corresponding to residues surrounding Thr291 of human IκBα |
Purification: |
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide was removed by chromatography using non-phosphopeptide corresponding to the phospholation site. |
Specificity/Sensitivity: |
IκBα(Phospho-Thr291 )antibody detects endogenous levels of IκBα only when phospholated at Threonine291 . |
Applications: |
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Background: |
In human glioblastoma cells, high glucose promotes hexokinase (HK) 2 dissociation from mitochondria and its subsequent binding and phosphorylation of IκBα at T291. Expression of IκBα T291A in glioblastoma cells blocked high glucose-induced PD-L1 expression and promoted CD8+ T cell activation and infiltration into the tumor tissue, reducing brain tumor growth[[1] . |
References: |
[1] Guo D, Tong Y, Jiang X, Meng Y, Jiang H, Du L, Wu Q, Li S, Luo S, Li M, Xiao L, He H, He X, Yu Q, Fang J, Lu Z. Aerobic glycolysis promotes tumor immune evasion by hexokinase2-mediated phosphorylation of IκBα. Cell Metab. 2022 Sep 6;34(9):1312-1324.e6. doi: 10.1016/j.cmet.2022.08.002. |
appl_detail: |
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