P1254
Brij® L23
suitable for Stein-Moore chromatography
동의어(들):
Brij 35, C12E23, Polyoxyethylene (23) lauryl ether
조직 및 계약 가격을 보려면 로그인를 클릭합니다.
크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
CAS 번호:
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12161900
MDL number:
description
non-ionic
Quality Level
form
solid
mol wt
micellar avg mol wt 48,000, estimated mol wt 1198
aggregation number
20-40
CMC
91 μM
transition temp
cloud point >100 °C
HLB
16.9
suitability
suitable for Stein-Moore chromatography
SMILES string
CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
InChI
1S/C58H118O24/c1-2-3-4-5-6-7-8-9-10-11-13-60-15-17-62-19-21-64-23-25-66-27-29-68-31-33-70-35-37-72-39-41-74-43-45-76-47-49-78-51-53-80-55-57-82-58-56-81-54-52-79-50-48-77-46-44-75-42-40-73-38-36-71-34-32-69-30-28-67-26-24-65-22-20-63-18-16-61-14-12-59/h59H,2-58H2,1H3
InChI key
IEQAICDLOKRSRL-UHFFFAOYSA-N
Application
Non-ionic detergent. Useful for the extraction of membrane proteins. Typically used in the range of 0.1-1%.
Legal Information
Brij is a registered trademark of Croda International PLC
Still not finding the right product?
Explore all of our products under Brij® L23
저장 등급
11 - Combustible Solids
wgk
WGK 2
flash_point_f
>300.2 °F - open cup
flash_point_c
> 149 °C - open cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
T Tobimatsu et al.
Archives of biochemistry and biophysics, 347(1), 132-140 (1997-11-05)
Recombinant adenosylcobalamin-dependent diol dehydratase of Klebsiella oxytoca overexpressed in Escherichia coli was purified to homogeneity. The enzyme has a low solubility and was extracted from the crude membrane fraction with 1% Brij 35 in a high recovery. Subsequent chromatography on
K Yamamoto et al.
Biochimica et biophysica acta, 790(3), 208-218 (1984-11-09)
Two forms of an acid proteinase have been purified from human erythrocyte membranes by a simple method involving selective extraction with 0.5% Brij 35, affinity chromatography on pepstatin A-Sepharose 4B, and chromatography on Sephacryl S-200 and DEAE-Sephadex G-100. One species
Darío Morais et al.
Rhinology, 50(1), 80-86 (2012-04-04)
Hereditary Haemorrhagic Telangiectasia or Rendu-Osler-Weber syndrome is a rare autosomal dominant vascular disease characterized by mucocutaneous and gastrointestinal telangiectases and localized arteriovenous malformations in lung, brain and liver. Epistaxis, due to rupture of telangiectases of the nasal mucosa, is the