推荐产品
产品名称
L-Lysine p-nitroanilide dihydrobromide,
方案
≥98% (TLC)
质量水平
表单
powder
技术
ligand binding assay: suitable
颜色
white to off-white
储存温度
2-8°C
SMILES字符串
Br.NCCCC[C@H](N)C(=O)Nc1ccc(cc1)N(=O)=O
InChI
1S/C12H18N4O3.BrH/c13-8-2-1-3-11(14)12(17)15-9-4-6-10(7-5-9)16(18)19;/h4-7,11H,1-3,8,13-14H2,(H,15,17);1H/t11-;/m0./s1
InChI key
FJNCJWJSSUJZMS-MERQFXBCSA-N
应用
L-Lysine p-nitroanilide may be used as a substrate to study the specificity and kinetics of lysine aminopeptidase(s) and various proteinases.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Bernardo Ramírez-Zavala et al.
FEMS microbiology letters, 235(2), 369-375 (2004-06-09)
A lysine aminopeptidase was purified from the yeast Kluyveromyces marxianus. This enzyme was purified 100-fold from a soluble extract obtained at 100,000g. The purification procedure consisted in fractionated precipitation with ammonium sulfate and five chromatography steps. The native enzyme had
Natasa Bozić et al.
Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 134(2), 231-241 (2003-02-06)
Exopeptidases of Morimus funereus larvae were partially purified and characterized. Specific leucyl aminopeptidase (LAP) activity was increased eight-fold by gel filtration of the crude midgut extract. The partially purified LAP had a molecular mass greater than 100 kDa with pH
Akifumi Kawamura et al.
Biomacromolecules, 6(2), 627-631 (2005-03-15)
The amidase activity of bovine pancreas trypsin in water-soluble complexes with poly(ethylene glycol)-block-poly(alpha,beta-aspartic acid) (PEG-PAA) was evaluated by a colorimetric assay using L-lysine p-nitroanilide as a substrate. The enzymatic reaction of trypsin was accelerated through the complexation with PEG-PAA. By
Priscilla L Phillips et al.
PloS one, 13(11), e0207295-e0207295 (2018-11-13)
The oral obligate anaerobe Porphyromonas gingivalis possesses a small conserved transcript PG_RS02100 of unknown function we previously identified using small RNA-seq analysis as expressed during logarithmic growth. In this study, we sought to determine if PG_RS02100 plays a role in
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