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- 详细信息
- 文献和实验
- 技术资料
- 库存:
50
- 供应商:
LSM BIO
- 检测范围:
78-5000pg/ml
- 检测方法:
夹心法ELISA
- 应用:
检测小鼠血清,血浆,组织匀浆内的目标蛋白含量
- 适应物种:
小鼠
- 标记物:
ATP synthase subunit b, mitochondrial, Atp5f1
- 样本:
小鼠血清,血浆,组织匀浆
- 灵敏度:
39pg/ml
- 规格:
96Tests
Mouse ATP synthase subunit b, mitochondrial, Atp5f1 ELISA KIT
Product Name:Mouse ATP synthase subunit b, mitochondrial, Atp5f1 ELISA KIT
Packing:96T
Catalog No.:ELI-49593m
Gene Name:Mouse Atp5f1
Detect Range:31.25-2000pg/ml
Sensitivity:18.75pg/ml
Target Protein Name:Mouse Atp5f1
Alternative Name:Mouse ATP synthase subunit b, mitochondrial, Atp5f1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse ATP synthase subunit b, mitochondrial, Atp5f1 ELISA KIT allows for the in vitro quantitative determination of Mouse Atp5f1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse ATP synthase subunit b, mitochondrial, Atp5f1 ELISA KIT has been pre-coated with an Mouse ATP synthase subunit b, mitochondrial, Atp5f1 antibody specific to Mouse Atp5f1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Atp5f1 and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Mouse Atp5f1 , biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.The concentration of Mouse Atp5f1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
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文献和实验Identification of Mutations in mtDNA from Patients Suffering Mitochondrial Diseases
The human mitochondrial genome. The structural genes for the mtDNA-encoded 12S and 16S ribosomal RNAs, the subunits of NADH-coenzyme Q oxidoreductase (ND), cytochrome-c oxidase (COX), cytochrome-b (Cyt b), and ATP synthase (A), and 22 tRNAs, are shown
Analysis of Human Mitochondrial DNA Mutations
genome. The structural genes for the mtDNAencoded 12S and 16S ribosomal RNAs, the subunits of NADH -coenzyme Q oxidoreductase (ND) , cytochrome c oxidase (COX) , cytochrome b (Cyt b) , and ATP synthase (A)
(ubiquinol cytochrome c oxido reductase or bc1 complex), IV (cytochrome c oxidase), and V (ATP synthase). These respiratory complexes are conserved from the yeast Saccharomyces cerevisiae to human with the exception of complex I, which is replaced
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