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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
武汉研升生物科有限公司
- 检测范围:
0.16-10 ng/mL
- 检测方法:
Sandwich
- 适应物种:
Mouse
- 样本:
tissue homogenates, cell lysates and other biological fluids
- 灵敏度:
0.062 ng/mL
- 规格:
48T/96T
| 规格: | 48T | 产品价格: | ¥1820.0 |
|---|---|---|---|
| 规格: | 96T | 产品价格: | ¥2600.0 |
| 中文名称 | 小鼠Fission 1蛋白(FIS1)酶联免疫吸附检测试剂盒 |
| 英文名称 | Mouse FIS1(Fission 1) ELISA Kit |
| 别名 | CGI-135; TTC11; Tetratricopeptide Repeat Domain 11; Mitochondrial fission 1 protein |
| 货号 | ELK0984 |
| 反应种属 | Mouse |
| Q9CQ92 | Q9CQ92 |
| 检测类型 | Sandwich |
| 灵敏度 | 0.062 ng/mL |
| 标准品 | 10 ng/mL |
| 检测范围 | 0.16-10 ng/mL |
| 样本类型 | tissue homogenates, cell lysates and other biological fluids |
| 反应时间 | 3.5h |
| 检测原理 | The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mouse FIS1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mouse FIS1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mouse FIS1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mouse FIS1 in the samples is then determined by comparing the OD of the samples to the standard curve. |
| 研究领域 | Tumor immunity; |

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文献和实验在现代生物医学研究及临床应用领域,酶联免疫吸附检测术(Enzyme-Linked ImmunoSorbent Assay,ELISA)的使用越来越广。在免疫学研究中,常见的ELISA应用包括检测体液或培养液中抗原(如细胞因子)或抗体的浓度。虽然ELISA技术的操作流程因具体实验目的不同而有差异,其基本思路均是先将已知抗体(或抗原)固定于酶联反应板上,利用抗原-抗体特异性结合的特点,使待检测样本中相应的抗原(或抗体)联结在酶联板上,然后利用针对待检测抗体或抗原的抗体及随后的酶促反应,测定样本中
Reliable Method for Detection of Programmed Cell Death in Yeast
and strains lacking the mitochondrial fission genes DNM1 /Drp1 and FIS1 , orthologs of mammalian cell death regulators. Cell viability following treatment with acetic acid is quantified by colony formation and vital dye (FUN1) staining to reproducibly detect
其对底物作用的活力,因而测出的酶活力直接反映游离的酶标记物。均相EIA在临床检验中较少应用。非均相EIA需先进行游离的和结合的标记物的分离。如前所述,固相载体可用作一种分离手段。这种固相酶免疫测定方法在1971年最初建立时称为酶联免疫吸附剂测定(enzyme linked immunosorbent assay),简称ELISA,在国内有译作酶联免疫吸附试验或酶标,已习用。
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