There is no specified method for the purification of product 534641. The following article has information on the purification of Amano lipase PS: https://www.sciencedirect.com/science/article/pii/S1359511322002057
534641
Amano Lipase PS, from Burkholderia cepacia
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Synonym(s):
APS-BCL, Pseudomonas cepacia (APS-PCL)
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10 G
€83.90
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€187.00
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10 G
€83.90
50 G
€187.00
About This Item
Recommended Products
Quality Level
specific activity
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Application
Amano Lipase PS is generally used in the enantioselective transesterification and hydrolysis.[1] Applications include:
- Lipase catalyzed transesterification of prochiral pyrimidine acyclonucleoside.[2]
- Lipase catalyzed hydrolysis of diacetylated pyrimidine acyclonucleosides.[3]
- Enantiomer selective acylation of racemic alcohols in continuous-flow bioreactors.[4]
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Resp. Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Enantiomer selective acylation of racemic alcohols by lipases in continuous-flow bioreactors.
Csajagi C, et al.
Tetrahedron Asymmetry, 19(2), 237-246 (2008)
Reverse Stereoselectivity in the Lipase-Catalyzed Hydrolysis of Diacetylated Pyrimidine Acyclonucleosides.
Kolodziejska et al.
ChemCatChem, 8(23), 3644-3649 (2016)
Lipase-catalyzed enantioselective transesterification of prochiral 1-((1, 3-dihydroxypropan-2-yloxy) methyl)-5, 6, 7, 8-tetrahydroquinazoline-2, 4 (1H, 3H)-dione in ionic liquids.
Kolodziejska, et al.
Chirality, 30(2), 206-214 (2018)
Immobilization of lipase from Burkholderia cepacia into calcium carbonate microcapsule and its use for enzymatic reactions in organic and aqueous media.
Fujiwara M, et al.
Journal of Molecular Catalysis. B, Enzymatic, 109, 94-100 (2014)
Dominik Koszelewski et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(43), 10156-10164 (2019-05-29)
A new protocol based on lipase-catalyzed tandem reaction toward α,β-enones/enoesters is presented. For the synthesis of the desired products the tandem process based on enzyme-catalyzed hydrolysis and Knoevenagel reaction starting from enol acetates and aldehyde is developed. The relevant impact
Articles
Efficient epimerization catalyst for enzyme mediated dynamic kinetic resolution (DKR).
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Is there any method for protein purification? The amount of protein in this product I got from the BCA analysis is only around 3%. I need the extract. thank you.
1 answer-
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What is the composition of this powder product ? I figured out that protein content is about 3%. Is This offered as an enzyme powder containing things like propylene glycol or calcium chloride? please answer me as much detail as possible. Thank you.
1 answer-
This product is tested for lipase activity. The purity and complete composition of this enzyme have not been determined.
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