추천 제품
설명
non-ionic
분석
≥98%
형태
powder
분자량
335.44 g/mol
기술
protein expression: suitable
CMC
19-25 mM (20-25°C)
적합성
suitable for molecular biology
응용 분야
life science and biopharma
SMILES string
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Functional assembly of 260-kDa oligomers required for mosquito-larvicidal activity of the Bacillus thuringiensis Cry4Ba toxin
Peptides (2015)
Conserved Properties of Polypeptide Transport-associated (POTRA) Domains Derived from Cyanobacterial Omp85*
The Journal of Biological Chemistry (2010)
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
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
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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