추천 제품
사용
sufficient for 100 colorimetric tests (with TNB standard)
검출 방법
colorimetric
관련 질환(들)
cancer; gastrointestinal diseases; pulmonary disorders
저장 온도
−20°C
일반 설명
The lipase family of enzymes catalyze the cleavage of the ester bonds of lipids. In mammals, this family includes many critical members including pancreatic, hepatic, endothelial, and lipoprotein lipase. Lipases, such as pancreatic lipase, are critical for the metabolism of lipids. Lipases also play key roles in processes such as cell signaling and inflammation. Measurements of lipase activity are commonly used to screen for pancreatic injury or disease, and to monitor diseases such as cystic fibrosis, celiac disease, and Crohn′s disease.
애플리케이션
Lipase Activity Assay Kit II has been used to measure lipase activity.
특징 및 장점
Compatible with high-throughput handling systems.
적합성
Suitable for the detection of lipase activity in biological samples including tissue, cells and serum
원리
The Lipase Activity Assay kit provides a simple and direct procedure for measuring lipase activity in a variety of samples. Lipase activity is determined using a coupled enzyme reaction, which results in a colorimetric (412 nm) product proportional to the enzymatic activity present. One unit of Lipase is the amount of enzyme that will generate 1.0 μmole of TNB per minute at 37 °C.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Resp. Sens. 1
Storage Class Code
3 - Flammable liquids
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시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
Inflammatory response of disc cells against Propionibacterium acnes depends on the presence of lumbar Modic changes.
Dudli S, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society, 27(5), 1013-1020 (2018)
Jervian Johnson et al.
3 Biotech, 11(7), 360-360 (2021-07-24)
In this study, hydrolytic and oxidative activities of enzymes isolated from halophilic microbes were characterized and applied for biomass utilization. First, lipase from Micrococcus luteus, and peroxidase and laccase from Pseudoalteromonas phenolica and Pseudoalteromonas peptidolytica were selected and their catalytic
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