推荐产品
方案
≥90% (TLC)
溶解性
methanol: 1 mg/mL, clear, slightly yellow to deep yellow
荧光
λex 360 nm; λem 530 nm±10 nm in methanol
适用性
suitable for fluorescence
储存温度
−20°C
SMILES字符串
CN(C)c1cccc2c(cccc12)S(=O)(=O)NCCN
InChI
1S/C14H19N3O2S/c1-17(2)13-7-3-6-12-11(13)5-4-8-14(12)20(18,19)16-10-9-15/h3-8,16H,9-10,15H2,1-2H3
InChI key
CSJXLKVNKAXFSI-UHFFFAOYSA-N
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警示用语:
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Biophysical journal, 69(5), 2024-2032 (1995-11-01)
Gln-41 on G-actin was specifically labeled with a fluorescent probe, dansyl ethylenediamine (DED), via transglutaminase reaction to explore the conformational changes in subdomain 2 of actin. Replacement of Ca2+ with Mg2+ and ATP with ADP on G-actin produced large changes
Biophysical journal, 70(3), 1439-1446 (1996-03-01)
Actin labeled at Gln-41 with dansyl ethylenediamine (DED) via transglutaminase reaction was used for monitoring the interaction of myosin subfragment 1 (S1) with the His-40-Gly-42 site in the 38-52 loop on F-actin. Proteolytic digestions of F-actin with subtilisin and trypsin
Journal of the American Chemical Society, 125(15), 4593-4599 (2003-04-10)
The binding of copper(II) ions to membrane-bound synthetic receptors has been investigated. Complexation fitted a 4:1 receptor:copper(II) model, and the observed binding constants are significantly enhanced at the membrane relative to solution; these effects can be explained by the lower
BMC biochemistry, 18(1), 3-3 (2017-03-08)
Histatins are histidine rich polypeptides produced in the parotid and submandibular gland and secreted into the saliva. Histatin-3 and -5 are the most important polycationic histatins. They possess antimicrobial activity against fungi such as Candida albicans. Histatin-5 has a higher
Biophysical journal, 71(4), 1914-1919 (1996-10-01)
The recently reported structural connectivity in F-actin between the DNase I binding loop on actin (residues 38-52) and the C-terminus region was investigated by fluorescence and proteolytic digestion methods. The binding of copper to Cys-374 on F- but not G-actin
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