- 询价
- 北京安必奇
- 5-100 ng/mL
- 0.1 ng/mL
- DEIA-BJ2162
- 2026年07月14日
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- 文献和实验
- 技术资料
- 库存：
In Stock
- 检测范围：
5-100 ng/mL
- 检测方法：
Competitive ELISA
- 应用：
Quantitative
- 样本：
Serum, plasma, cell culture supernatants, body fluid and tissue homogenate
- 灵敏度：
0.1 ng/mL
- 规格：
96T
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文献和实验RAT/MOUSE GROWTH HORMONE ELISA KIT
实验原理 This assay is a Sandwich ELISA based, sequentially, on: 1) capture of rat or mouse Growth Hormone molecules from samples to the wells of a microtiter plate coated by a pre-titered amount of anti-Growth Hormone
at 4°C for 15 minutes. 9. Remove and aliquot supernatant. We recommend making several 50 μl aliquots. 10. Before running ELISA, dilute protein 1:100 and run a Bradford total protein assay or Quant-iT™ Protein Quantitation Kit assay (Cat. no. Q
Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar
complex, with K d =10−14 M , half-life of about 2 d and an association rate constant of 4�108 M −1 /s. The kinetic and thermodynamics of the barnase-barstar interaction were investigated in detail (12 –20 ). High affinity is maintained at pH 7.0–
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