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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Recombinant human protein was used as the immunogen for this Thymidylate synthase antibody.
- 保存条件:
Aliquot and Store at 2-8℃
- 保质期:
1年
- 级别:
科研级别
- 库存:
100
- 供应商:
艾美捷科技
- 宿主:
小鼠
- 应用范围:
IHC, IF
- 抗体英文名:
Thymidylate Synthase Antibody [TYSY9]
- 抗体名:
Thymidylate Synthase Antibody [TYSY9]
- 规格:
100ug
Thymidylate Synthase 抗体 [TYSY9],Thymidylate Synthase Antibody [TYSY9],Thymidylate Synthase 抗体 [TYSY9],Thymidylate Synthase Antibody [TYSY9]
产品名称:Thymidylate Synthase 抗体 [TYSY9]-Thymidylate Synthase Antibody [TYSY9]
产品货号:PSI-33-918-100ug
产品规格:100ug
背景资料:Thymidylate synthase converts deoxyuridine monophosphate (dUMP) to deoxythymidine monophosphate (dTMP), which is essential for DNA biosynthesis. Thymidylate synthase is also a critical target for the fluoropyrimidines, an important group of anti-neoplastic drugs that are widely used in the treatment of solid tumors. Both 5-FU and fluorodeoxyuridine are converted in tumor cells to FdUMP which inactivates thymidylate synthase by formation of a ternary covalent complex in the presence of the folate cofactor 5,10-methylenetetrahydrofolate. Expression of thymidylate synthase protein is associated with response to 5-fluorouracil (5-FU) in human colorectal, gastric, head and neck, and breast carcinomas.
保存建议:Thymidylate Synthase 抗体 [TYSY9]-Thymidylate Synthase Antibody [TYSY9]Aliquot and Store at 2-8℃
应用类型:IHC, IF
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文献和实验5-Fluorouracil Metabolizing Enzymes
intracellular conversion to form cytotoxic nucleotides (1 ). Several cellular targets for fluoropyrimidines have been well-characterized, including inhibition of thymidylate synthase (TS) by fluorodeoxyuridine monophosphate (FdUMP) and false base incorporation
Yeast Nuclear Genes for mtDNA Maintenance
1 (8 ), or the RNA polymerase RPO41 (9 ). Others encode cytoplasmic or nuclear proteins that control the synthesis, or the flux, of metabolites necessary for mitochondrial DNA synthesis, such as the thymidylate kinase (10 ), thymidylate synthase (10 ), or subunits
Evaluation of RNA Chaperone Activity In Vivo and In Vitro Using Misfolded Group I Ribozymes
is measured. Folding is evaluated indirectly by assessing the difference in splicing activity with or without proteins with RNA chaperone activity. In vitro, we use the thymidylate synthase (td ) group I intron of phage T4 that is split into two halves
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