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- 文献和实验
- 技术资料
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- 库存:
100+
- 供应商:
上海维亦特生物
- CAS号:
862778-57-2
Tris-NTA per-Tert-butyl Ester
862778-57-2
C₈₄H₁₄₈N₈O₂₄
1654.11
White to Pale Yellow Solid
Chloroform (Slightly), Methanol (Slightly)
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文献和实验Tris-NTA per-Tert-butyl Ester
862778-57-2
C₈₄H₁₄₈N₈O₂₄
1654.11
White to Pale Yellow Solid
Chloroform (Slightly), Methanol (Slightly)
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
LABELING MUSCLE ACTIN WITH CARBOXYFLUORESCEIN SUCCINIMIDYL ESTER
Day 0 and 1 Materials 1.0.5 mM ATP,0.2 mM CaCl2,1 mM PIPES,pH 6.8 at 4℃,250 ml for day 0. 2.0.5 mM ATP,0.2 mM CaCl2,70 mM KCl,150 mM PIPES,pH 7.0,1 ml. 3.16 mM ATP,0.2 mM CaCl2,5 mM DTT,5 mM lysine,10 mM glutamic acid,20 mM Tris-HCl,pH 8.0,10 ml
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
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