DNTP004533
dGTP
dNTP Pool | |
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Pool identifier | POOL001136 |
Members of this Pool |
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Members of control pools |
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POOL001067 |
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Last modified: 10/Sep/2021
Results | |
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Publication |
Hu CM, Tien SC, Hsieh PK, Jeng YM, Chang MC, Chang YT, Chen YJ, Chen YJ, Lee EYP, Lee WH: High Glucose Triggers Nucleotide Imbalance through O-GlcNAcylation of Key Enzymes and Induces KRAS Mutation in Pancreatic Cells.,
Cell Metab, 2019
PubMed |
Value | 0.2518 | Dimension | fold change |
Error (standard deviation) | 0.0989 |
Relative compared to | control |
Data presentation in publication | diagram |
Source | |
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Source organism |
human
(Homo sapiens)
Taxonomy 9606 |
Sample source | cell line |
Tissue type | mammary epithelial cells |
CLO Cell line name | MCF 10A cell (CLO:0007599) |
Cell line/type as in publication | MCF10A |
Compartment | whole cell |
Experiment Details | |
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Measurement type | dNTP incorporation assay |
Extraction method | methanol |
Remarks to measurement type | Ferraro |
Growth conditions | 3-day culture with 22 mM of glucose. |
Treatment | |
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Drug/stress type | drug |
PubChem | 5793 |
Applied drug | Glucose |
Treatment details/effects | the reductionof PFK activity that alters the glucose metabolic pathway contributes to the high-glucose-induced effects in pancreatic cells |
Genes and Proteins | |
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Gene name | PFKL |
Gene identifier | 5211 |
Protein name | ATP-dependent 6-phosphofructokinase, liver type |
Protein identifier | P17858 |
Genetic manipulation/variation | silencing |