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Merck

N1138

Sigma-Aldrich

N-Nonanoyl-N-methylglucamine

≥98%

别名:

N-(D-Glucityl)-N-methylnonanamide, N-Methyl-N-nonanoyl-D-glucamine, MEGA-9

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About This Item

经验公式(希尔记法):
C16H33NO6
CAS号:
分子量:
335.44
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.32

描述

non-ionic

化驗

≥98%

形狀

powder

分子量

335.44 g/mol

技術

protein expression: suitable

CMC

19-25 mM (20-25°C)

適合性

suitable for molecular biology

應用

life science and biopharma

SMILES 字串

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 密鑰

GCRLIVCNZWDCDE-SJXGUFTOSA-N

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應用

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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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)
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
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
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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