- ￥3627 - 5031
- Biorbyt
- 0.16-10ng/mL
- 0.1 ng/mL
- orb1948696
- 英国
- 2026年08月04日
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- 文献和实验
- 技术资料
- 库存：
99
- 供应商：
Biorbyt
- 检测范围：
0.16-10ng/mL
- 检测方法：
Sandwich
- 适应物种：
Human
- 样本：
serum, plasma, Tissue homogenate and Other biological samples
- 灵敏度：
0.1 ng/mL
- 规格：
48 T/96 T
| 规格： | 48 T | 产品价格： | ￥3627.0 |
|---|---|---|---|
| 规格： | 96 T | 产品价格： | ￥5031.0 |
描述: Human Squamous Cell Carcinoma Antigen 2 (SCCA2) ELISA Kit
别名: SERPINB4 , LEUPIN, PI11, SCCA-2,Serpin B4
靶点: SCCA2
应用说明: This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human SCCA2. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human SCCA2 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human SCCA2, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human SCCA2. You can calculate the concentration of Human SCCA2 in the samples by comparing the OD of the samples to the standard curve.
检测时间: 3.5H
标准品: 10ng/mL
研究领域: Cancer Biology; Immunology & Inflammation
UniProt ID: P48594
备注: For research use only.
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文献和实验31600篇！CUSABIO 7月文献引用再破记录，200篇新文献为科研助力
via ATF6 lactylation-mediated tryptophan metabolism in hepatocellular carcinoma 影响因子：30.9 发表期刊：Cell Metabolism CUSABIO助力产品： Human Kynurenine (KYN)ELISA Kit; CSB-E13659h 研究亮点 本研究揭示AARS1作为乳酰转移酶，在肝细胞癌中催化ATF6蛋白K424位点乳酰化，阻止其泛素化降解，稳定ATF6并转录激活TDO2，增强色氨酸代谢和L-
.W. well). This antibody will stain up practically all histological types of epithelial tumor, including glandular tumors, undifferentiated carcinomas, keratinizing squamous cell carcinoma, neuroendocrine carcinomas, small cell carcinomas
and cholangiocarcinoma cell lines and from tumor tissues. Comparison with DNA sequencing data confirmed the specificity of the ELISA-mediated mutation analysis. Epithelial cell content from stroma rich tissues was estimated by measuring the CK 8, 18 and 19 concentration
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