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- 文献和实验
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- 保存条件:
2-8°C
- 保质期:
6个月
- 库存:
100
- 供应商:
百欧泰
- 规格:
5ml/10ml
| 规格: | 5ml | 产品价格: | ¥1500.0 |
|---|---|---|---|
| 规格: | 10ml | 产品价格: | ¥2500.0 |
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文献和实验In-gel Tryptic Digest for Protein ID by Mass Spectrometry
or silver stained gel.Cut gel band into 1 mm cubes using clean razor blade on a clean glass surface.Transfer to an Eppendorf tube.2.Remove excess water with pipet.Add 25-35 μl acetonitrile to tube to cover gel pieces.Incubate 10 minutes at RT to dehydrate
of determining protein valence entails the calculation of net charge from amino acid sequence/composition. However, the inaccuracy of that approach was recognized long before the advent of the protein data banks and computer programs to facilitate its adoption
Use of Flow Cytometric Methods to Quantify Protein‐Protein Interactions
for the quantitative analysis of protein?protein interactions using the flow cytometry protein interaction assay (FCPIA). This method is based upon immobilizing protein on a polystyrene bead, incubating these beads with a fluorescently labeled binding partner
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