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- 文献和实验
- 技术资料
- 保存条件：
Recommended Refrigeration Conditions (2℃-8℃) for storage
- 英文名：
tert-butyl (6S)-6-amino-1,4-oxazepane-4-carboxylate
- 供应商：
南京鼎石
- CAS号：
1932377-93-9
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///13730kg
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文献和实验RNA Synthesis Using 2-O-(Tert-Butyldimethylsilyl) Protection
This chapter enables the reader to carry out the solid-phase synthesis of ribonucleic acid (RNA) using β-cyanoethyl phosphoramidite chemistry combined with tert -butyldimethylsilyl protection of the ribose 2′-hydroxyl group. Phosphoramidite
Native Gel Electrophoresis to Study the Binding and Release of RNA Polymerase by 6S RNA
protein complexes, which is often called band shift, gel retardation, or electrophoretic mobility shift assays. Gel shift assays have been used to study a plethora of RNA–protein interactions in all organisms, but here we will use the 6S RNA:RNA polymerase
Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group
The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties
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