所有图片(5)
别名:
N-(D-Glucityl)-N-methylnonanamide, N-Methyl-N-nonanoyl-D-glucamine, MEGA-9
经验公式（希尔记法）:
C16H33NO6
推荐产品
描述
non-ionic
质量水平
检测方案
≥98%
形式
powder
分子量
335.44 g/mol
技术
protein expression: suitable
CMC
19-25 mM (20-25°C)
适用性
suitable for molecular biology
应用
life science and biopharma
SMILES字符串
CCCCCCCCC(=O)N(C)C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
InChI
1S/C16H33NO6/c1-3-4-5-6-7-8-9-14(21)17(2)10-12(19)15(22)16(23)13(20)11-18/h12-13,15-16,18-20,22-23H,3-11H2,1-2H3/t12-,13+,15+,16+/m0/s1
InChI key
GCRLIVCNZWDCDE-SJXGUFTOSA-N
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应用
N-Nonanoyl-N-methylglucamine has been used to reconstitute proteins into liposomes. It has also been used to study its effects on the oligomerization of Bacillus thuringiensis Cry4Ba toxin.
Non-ionic, dialyzable detergent
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Functional assembly of 260-kDa oligomers required for mosquito-larvicidal activity of the Bacillus thuringiensis Cry4Ba toxin
Narumol Khomkhum
Peptides (2015)
Conserved Properties of Polypeptide Transport-associated (POTRA) Domains Derived from Cyanobacterial Omp85*
Patrick Koenig
The Journal of Biological Chemistry (2010)
K Häsler et al.
Biochemistry, 38(41), 13759-13765 (1999-10-16)
ATP synthase is conceived as a rotary enzyme. Proton flow drives the rotor (namely, subunits c12 epsilon gamma) relative to the stator (namely, subunits ab2 delta(alpha beta)3) and extrudes spontaneously formed ATP from three symmetrically arranged binding sites on (alpha
B Norling et al.
Biochimica et biophysica acta, 935(2), 123-129 (1988-09-14)
Isolation of F1-ATPase from Rhodospirillum rubrum by chloroform extraction of chromatophores, followed by purification on a glycerol gradient, results in a very pure enzyme preparation containing five subunits with high Ca2+-ATPase activity (15 mumol per min per mg protein). Furthermore
Dhanesh Gadre et al.
Journal of chromatography. A, 1575, 49-58 (2018-09-29)
Endotoxins are complex molecules and one of the most challenging impurities requiring separation in biopharmaceutical protein purification processes. Usually these contaminants are cleared during the downstream process, but if endotoxin interacts with the target protein it becomes difficult to remove.
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