推荐产品
等級
Biotechnology Performance Certified
無菌
0.2 μm filtered
濃度
1 M in solution
技術
cell culture | mammalian: suitable
雜質
DNase, RNase, Protease, none detected
bioburden, tested
endotoxin, tested
<5 ppm heavy metals as (Pb)
有用的pH值範圍
7.4-8.8
pKa (25 °C)
8.1
正離子痕跡
Fe: <5 ppm
SMILES 字串
OCC(CO)(CO)NCC(O)=O
InChI
1S/C6H13NO5/c8-2-6(3-9,4-10)7-1-5(11)12/h7-10H,1-4H2,(H,11,12)
InChI 密鑰
SEQKRHFRPICQDD-UHFFFAOYSA-N
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應用
用于分离低分子量的肽的缓冲剂组分。
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
Journal of separation science, 34(18), 2463-2467 (2011-08-06)
This paper compares different buffer systems for the electrophoretic separation of the five most abundant serum proteins on native-PAGE gel and cellulose membranes. A modified Tris-tricine system was shown to be superior for the separation of these serum proteins in
Neuropharmacology, 58(3), 676-681 (2009-11-17)
Glycine receptor function mediates most inhibitory neurotransmission in the brainstem and spinal cord and is enhanced by alcohols, volatile anesthetics, inhaled drugs of abuse, and endogenous compounds including zinc. Because zinc exists ubiquitously throughout the brain, investigations of its effects
Biofouling, 29(1), 77-85 (2012-12-06)
The freshwater zebra mussel (Dreissena polymorpha) is a notorious biofouling organism. It adheres to a variety of substrata underwater by means of a proteinaceous structure called the byssus, which consists of a number of threads with adhesive plaques at the
The Journal of general physiology, 139(3), 219-234 (2012-03-01)
Here, we describe a new mechanism by which glutamate (Glu) and trace metals reciprocally modulate activity of the Ca(v)2.3 channel by profoundly shifting its voltage-dependent gating. We show that zinc and copper, at physiologically relevant concentrations, occupy an extracellular binding
Methods in molecular biology (Clifton, N.J.), 869, 81-91 (2012-05-16)
Tricine-sodium dodecyl sulphate-polyacrylamide gel electrophoresis (tricine-SDS-PAGE) is an efficient way of separating low-molecular-mass proteins. However, the standard system is quite complicated and specifically may not be useful when the separated proteins require to be recovered from the gel for quantitative
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