- ￥3250
- biorbyt
- orb629768
- 英国
- 2025年12月04日
- ELISA, IHC, WB
- Rabbit
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
TYMP Antibody抗体
- 抗体英文名：
TYMP Antibody
- 靶点：
TYMP
- 应用范围：
ELISA, IHC, WB
- 宿主：
Rabbit
- 适应物种：
Human
- 保质期：
6-12个月
- 抗原来源：
详询
- 目录编号：
orb629768
- 级别：
科研级
- 库存：
88
- 供应商：
biorbyt
- 标记物：
Unconjugated
- 克隆性：
Polyclonal
- 形态：
liquid
- 亚型：
IgG
- 免疫原：
thymidine phosphorylase
- 规格：
50 ug
免疫原：thymidine phosphorylase
应用稀释比例：WB: 1:500-1:2000; IHC: 1:20-1:200
纯度:≥95% as determined by SDS-PAGE
纯化:Immunogen affinity purified
保存说明:Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
UniProt ID:P19971
Note:For research use only.
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文献和实验with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). Since the identification of mutations in TYMP , the gene encoding TP, as the cause of MNGIE (Nishino et al. Science 283:689–692, 1999), the assessment of TP dysfunction has become the best screening
Measurement of Mitochondrial DNA Copy Number
disorders characterized by a significant reduction in mtDNA content. These genes include POLG , DGUOK , TK2 , TYMP , MPV17 , SUCLA2 , SUCLG1 , RRM2B , and C10orf2 , all nine genes have mutations reported to cause various forms of MDDSs. In this chapter
Real‐Time Quantitative PCR Analysis of Mitochondrial DNA Content
. The mitochondrial DNA (mtDNA) depletion syndromes (MDDSs) are autosomal recessive disorders caused by molecular defects in nuclear genes, and characterized by a reduction in mtDNA content. To date, mutations in at least nine genes (POLG , DGUOK , TK2 , TYMP , MPV
技术资料暂无技术资料 索取技术资料
