추천 제품
생물학적 소스
fungus (Candida antarctica)
재조합
expressed in Aspergillus oryzae
형태
beads
특이 활성도
≥1800 U/g
기술
analytical sample preparation: suitable
색상
white to off-white
응용 분야
life science and biopharma
저장 온도
2-8°C
유전자 정보
fungus ... LIPB(1170790)
일반 설명
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.
애플리케이션
Lipases are used industrially for the resolution of chiral compounds and the transesterification production of biodiesel.
생화학적/생리학적 작용
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.
단위 정의
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
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.
이미 열람한 고객
Biotechnological relevance of the lipase A from Candida antarctica
Monteiro RRC, et al.
Catalysis Today, 362, 141-154 (2021)
Interfacial activation of Candida antarctica lipase B: combined evidence from experiment and simulation
Themistoklis Z, et al.
Biochemistry, 54(38), 5969?5979- 5969?5979 (2015)
Karel Pomeisl et al.
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
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