54326
Lipase B Candida antarctica immobilized on Immobead 150, recombinant from Aspergillus oryzae
≥1800 U/g
Synonym(s):
Candida lipase, Immobilized lipase, Recombinant lipase
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
biological source
fungus (Candida antarctica)
Quality Level
recombinant
expressed in Aspergillus oryzae
form
beads
specific activity
≥1800 U/g
technique(s)
analytical sample preparation: suitable
color
white to off-white
application(s)
life science and biopharma
storage temp.
2-8°C
Gene Information
fungus ... LIPB(1170790)
General description
Research area: Cell Signaling
Lipase B from Candida antarctica (CAL-B) is a serine hydrolase, α/β-hydrolase, and is a member of the lipase family. CAL-B is composed of an α/β-hydrolase fold and the active site contains a Ser-His-Asp catalytic triad.
Lipase B from Candida antarctica (CAL-B) is a serine hydrolase, α/β-hydrolase, and is a member of the lipase family. CAL-B is composed of an α/β-hydrolase fold and the active site contains a Ser-His-Asp catalytic triad.
Application
Lipases are used industrially for the resolution of chiral compounds and the transesterification production of biodiesel.
Biochem/physiol Actions
Lipase B from Candida antarctica (CAL-B) acts as a catalyst for producing amines, amides, and alcohols.. It is used as a biocatalyst in research and industry. CAL-B is involved in the hydrolysis of triglycerides. Lipases catalyze the hydrolysis of triacylglycerols into glycerol and free fatty acids.
Unit Definition
1 U corresponds to the amount of enzyme which liberates 1 μmol butyric acid per minute at pH 7.5 and 40°C (tributyrin, Cat. No. 91010, as substrate)
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Bioorganic & medicinal chemistry, 27(7), 1246-1253 (2019-02-20)
An enzymatic alternative to the chemical synthesis of chiral gem-difluorinated alcohols has been developed. The method is highly effective and stereoselective, feasible at laboratory temperature, avoiding the use of toxic heavy metal catalysts which is an important benefit in medicinal
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service