- ￥3510
- biorbyt
- 0.32-20ng/mL
- 0.19 ng/mL
- orb1948576
- 英国
- 2026年01月21日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
999
- 供应商：
biorbyt
- 检测范围：
0.32-20ng/mL
- 检测方法：
Sandwich
- 适应物种：
Human
- 样本：
serum, plasma, Tissue homogenate and Other biological samples
- 灵敏度：
0.19 ng/mL
- 规格：
48 T
产品别名：Heat shock protein 9kDa beta member 1 ,HSP9B1, endoplasmin,gp96,grp94, ERp99
应用笔记：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 HSP gp96. 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 HSP gp96 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 HSP gp96, 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 HSP gp96. You can calculate the concentration of Human HSP gp96 in the samples by comparing the OD of the samples to the standard curve.
实验时长：3.5H
靶点：HSP gp96
Note：For research use only.
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文献和实验Cellular stress proteins like the classical heat-shock proteins (HSPs) hsp70 (1 –3 ), hsp90 (3 ) and hsp110 (4 ); the glucose-regulated proteins gp96/GRP94 (3 ,5 ) and grp170 (4 ); as well as the endoplasmic chaperone calreticulin
Analysis of Heat-Shock Protein Localisation Using Flow Cytometry
The use of flow cytometry in heat-shock protein (HSP) research is increasing rapidly due to the high sensitivity and versatility of the technique. The method allows the simultaneous analysis of multiple proteins within numerous cell types
Stress Response Profiles in Human Fibroblasts Exposed to Heat Shock or Oxidative Stress
demonstrated a specific upregulation of Hsp70 mRNA and protein after heat shock, while heme oxygenase 1 (HO1 or Hsp32) mRNA and protein was specifically upregulated following H2 O2 -induced oxidative stress. Hsp70 and HO1 should therefore be considered
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