P6501
Phenyl-β-D-galactopyranoside
≥98% (TLC)
동의어(들):
P-Gal, Phenyl β-D-galactoside
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C12H16O6
CAS 번호:
Molecular Weight:
256.25
Beilstein:
87518
EC Number:
MDL number:
UNSPSC 코드:
41141627
PubChem Substance ID:
NACRES:
NA.52
일반 설명
Phenyl-β-D-galactopyranoside is used as a substrate for detecting β-galactosidase enzymatic activity.
애플리케이션
Phenyl-β-D-galactopyranoside has been used in mutant phage screening.
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)
Jules A A C Heuberger et al.
The Lancet. Haematology, 4(8), e374-e386 (2017-07-04)
Substances that potentially enhance performance (eg, recombinant human erythropoietin [rHuEPO]) are considered doping and are therefore forbidden in sports; however, the scientific evidence behind doping is frequently weak. We aimed to determine the effects of rHuEPO treatment in well trained
E J Mientjes et al.
Mutation research, 360(2), 101-106 (1996-06-10)
The recent introduction of the phenyl-beta-D-galactopyranoside (P-gal)-based positive-selection system for screening of lambda lacZ phages originating from the lambda lacZ transgenic mouse (Muta Mouse) has made the determination of mutant frequencies (MF) a much simpler task. Previously, MF data from
J P Cai et al.
Nucleic acids research, 25(6), 1170-1176 (1997-03-15)
8-Oxo-7,8-dihydro-2'-deoxyguanosine 5'-triphosphate (8-oxo-dGTP) is produced during normal cellular metabolism, and incorporation into DNA causes transversion mutation. Organisms possess an enzyme, 8-oxo-dGTPase, which catalyzes the hydrolysis of 8-oxo-dGTP to the corresponding nucleoside monophosphate, thereby preventing the occurrence of mutation. There are
Jiri Kos et al.
Molecules (Basel, Switzerland), 16(5), 3740-3760 (2011-05-06)
The gastrointestinal absorption of bisphosphonates is in general only about 1%. To address this problem mixtures of risedronate monosodium salt with twelve varied sugar alcohols, furanoses, pyranoses and eight gluco-, manno- and galactopyranoside derivatives as counterions were designed in an
M M Palcic et al.
The Journal of biological chemistry, 264(29), 17174-17181 (1989-10-15)
Porcine submaxillary beta-galactoside alpha(1----2)-fucosyltransferase is known to transfer a fucosyl residue from guanosine 5'-diphosphofucose (GDP-fucose) to the 2-OH group of beta-D-galactopyranosides with inversion of configuration at the fucopyranosyl anomeric carbon. A bisubstrate analog (1) of the postulated transition-state for this
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