- ￥3003 - 9483
- TargetMol
- 美国
- T20837
- 2026年01月10日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
零下80~20°C
- 保质期：
Powder: -20°C for 3 years In solvent: -80°C for 2 years
- 英文名：
Fmoc-N-amido-PEG12-acid
- 库存：
10
- 供应商：
TargetMol
- CAS号：
850312-72-0
- 规格：
1 g/500 mg/100 mg
| 规格： | 1 g | 产品价格： | ￥9483.0 |
|---|---|---|---|
| 规格： | 500 mg | 产品价格： | ￥6243.0 |
| 规格： | 100 mg | 产品价格： | ￥3003.0 |
Product Introduction
Bioactivity
英文名:Fmoc-N-amido-PEG12-acid
描述:Fmoc-N-amido-PEG12-acid is a PEG derivative, it contains a Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. Under the basic conditions, the Fmoc group can be deprotected to obtain the free amine for further conjugations.
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文献和实验) to check derivatisation and chromatography efficiency and to allow quantitation of samples. Note that the Fmoc-amino acid derivatives are stable for 24 h, allowing many samples to be prepared in advance and loaded onto an autosampler for injection
nonglycosylated peptide is first synthesized on a solid-phase support using standard Fmoc chemistry. The glycosylation site is then introduced through an orthogonally protected 2-phenylisopropyl (PhiPr) aspartic acid (Asp) residue. After selective deprotection
Synthesis and Probing of Membrane-bound Peptide Arrays
from their carboxyl termini using Fmoc-amino acid derivatives. After completion of the synthesis and cleavage of all side-chain protecting groups, the peptide array on the membrane is incubated with the potential interaction partners to identify their target sequences
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