(2S)-2-((((9H-Fluoren-9-yl)Met
hoxy)carbonyl)aMino)-2-(4-hydroxycyclohexyl)aceticacid/1416444-92-2- ￥1068
- 麦克林
- S849669-250mg
- 2026年03月11日
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
(2S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-2-(4-hydroxycyclohexyl)aceticacid
- 库存：
999
- 供应商：
上海麦克林生化科技股份有限公司
- CAS号：
1416444-92-2
- 规格：
250mg
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文献和实验group?specific modifications of amino groups. These reactions remain valid tools for early?stage evaluation of structure?function relationships, but are now valued even more for their applications in the preparation of bioconjugates, affinity columns
Acetylation (or Succinylation) of Amino Groups on Proteins
Acetylation (or Succinylation) of Amino Groups on Proteins REFERENCE: Hanock and Benz. 1986. BBA. 860:699-707. PURPOSE: Derivitization of amino groups to remove the positive charge characteristics of the protein, for example
Synthesis and Application of Highly Reactive Amino Linkers for Functional Oligonucleotides
are functionalized by conjugation with a variety of molecules, and aliphatic amino linkers have been frequently used as a tether for their modifications. This unit describes the syntheses and applications of novel amino linkers having a carbamate structure
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