1-832-868-1888
order@swbio.com
Catalog Number: |
58023 |
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 Ser180/183 of human PRPS1/2 |
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: |
PRPS1/2(Phospho- Ser180/183)antibody detects endogenous levels of PRPS1/2 only when phospholated at Serine180/183 . |
Applications: |
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Background: |
Glucose deprivation or hypoxia results in the AMPK-mediated phosphorylation of phosphoribosyl pyrophosphate synthetase 1 (PRPS1) S180 and PRPS2 S183, AMPK converts PRPS1/2 hexamers to monomers, and inhibits PRPS1/2 activity and subsequent nucleotide and NAD synthesis to maintain tumor cell growth and survival. The expression of nonphosphorylatable PRPS1/2 mutants greatly decreased cellular ATP and NADPH levels, increased reactive oxygen species (ROS) levels and cell apoptosis, and inhibited brain tumorigenesis [1] . |
References: |
[1] Qian X, Li X, Tan L, Lee JH, Xia Y, Cai Q, Zheng Y, Wang H, Lorenzi PL, Lu Z. Conversion of PRPS Hexamer to Monomer by AMPK-Mediated Phosphorylation Inhibits Nucleotide Synthesis in Response to Energy Stress. Cancer Discov. 2018 Jan;8(1):94-107. doi: 10.1158/2159-8290.CD-17-0712. |
appl_detail: |
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