推荐产品
质量水平
方案
≥90% (TLC)
表单
powder
储存温度
2-8°C
SMILES字符串
OC(=O)c1cc(nc2ccccc12)-c3cc(C(O)=O)c4ccccc4n3
InChI
1S/C20H12N2O4/c23-19(24)13-9-17(21-15-7-3-1-5-11(13)15)18-10-14(20(25)26)12-6-2-4-8-16(12)22-18/h1-10H,(H,23,24)(H,25,26)
InChI key
AFYNADDZULBEJA-UHFFFAOYSA-N
应用
2,2′-Biquinoline-4,4′-dicarboxylic acid has been used in a study that synthesized and structurally characterized six metal-organic coordination polymers.
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)
Sandeep Kumar Vashist et al.
Biochemical and biophysical research communications, 411(2), 455-457 (2011-07-19)
We report here substantial interference from N-hydroxysuccinimide (NHS) in the bicinchoninic acid (BCA) protein assay. NHS is one of the most commonly used crosslinking agents in bioanalytical sciences, which can lead to serious potential errors in the BCA protein assay
J P Dean Goldring
Methods in molecular biology (Clifton, N.J.), 869, 29-35 (2012-05-16)
During each step of a protein isolation technique, if enzyme activity is to be determined and before a protein mixture is separated on a polyacrylamide electrophoresis gel, it is important to determine the concentration of the protein(s) in solution. Measuring
Wijitar Dungchai et al.
The Analyst, 136(1), 77-82 (2010-09-28)
Wax screen-printing as a low-cost, simple, and rapid method for fabricating paper-based microfluidic devices (µPADs) is reported here. Solid wax was rubbed through a screen onto paper filters. The printed wax was then melted into the paper to form hydrophobic
Randall I Krohn
Current protocols in cell biology, Appendix 3, 3H-3H (2011-09-08)
Protein quantification is an important step for handling protein samples for isolation and characterization; it is a prerequisite step before submitting proteins for chromatographic, electrophoretic, or immunochemical analysis and separation. Colorimetric methods are fast, simple, and not laborious. This unit
Baoyan Bai et al.
Proteomics, 12(19-20), 3044-3048 (2012-08-15)
Efficient extraction and accurate quantification of nucleolar macromolecules are critical for in vitro analysis, especially for studying RNA, DNA, and protein dynamics under identical conditions. There is presently no single method that efficiently and simultaneously isolates these three macromolecular constituents
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