Catalase Activity Assay试剂盒(Colorimetric/Fluorometric) (ab83464)
Key features and details
- Assay type: Enzyme activity (quantitative)
- Detection method: Colorimetric/Fluorometric
- Platform: Microplate reader
- Assay time: 40 min
- Sample type: Cell Lysate, Plasma, Serum, Tissue Lysate
概述
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产品名称
Catalase Activity Assay试剂盒(Colorimetric/Fluorometric)
参阅全部 Catalase 试剂盒 -
检测方法
Colorimetric/Fluorometric -
样品类型
Serum, Plasma, Cell Lysate, Tissue Lysate -
检测类型
Enzyme activity (quantitative) -
检测时间
0h 40m -
种属反应性
与反应: Mammals -
产品概述
Catalase Activity Assay Kit (Colorimetric/Fluorometric) (ab83464) is a highly sensitive, simple and direct assay for measuring catalase activity in a variety of biological samples such as cell and tissue lysates or biological fluids.
In the catalase activity assay protocol, the catalase present in the sample reacts with hydrogen peroxide (H2O2) to produce water and oxygen. The unconverted H2O2 reacts with probe to produce a product that can be measured colorimetrically at OD 570 nm or fluorometrically at Ex/Em = 535/587 nm. Therefore, the catalase activity present in the sample is reversely proportional to the signal obtained. The kit can detect as little as 1 µU of catalase activity.
Catalase activity assay protocol summary:
- add samples and standards to wells
- add stop solution into sample control wells and incubate at 25ºC for 5 min
- add H2O2 solution into wells and incubate for 30 min at 25ºC
- add stop solution
- add developer mix and incubate for 10 min at 25ºC
- analyze with microplate reader
Technical Note: This assay is not recommended for use in urine samples due to the presense of reducing agents.
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说明
This product is manufactured by BioVision, an Abcam company and was previously called K773 Catalase Activity Colorimetric/Fluorometric Assay Kit. K773-100 is the same size as the 100 test size of ab83464.
The Safety Datasheet for this product has been updated for certain countries. Please check the current version in the SDS download section.
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平台
Microplate reader
性能
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存放说明
Store at -20°C. Please refer to protocols. -
组件 100 tests 2000 tests Assay Buffer VIII 1 x 25ml 20 x 25ml Catalase Positive Control 1 x 20µl 20 x 20µl Developer Solution V 1 vial 20 vials Hydrogen Peroxide Solution III 1 x 25µl 20 x 25µl OxiRed Probe 1 x 200µl 20 x 200µl Stop Solution III 1 x 1ml 20 x 1ml -
研究领域
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功能
Occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells. -
疾病相关
Defects in CAT are the cause of acatalasia (ACATLAS) [MIM:115500]; also known as acatalasemia. This disease is characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions. -
序列相似性
Belongs to the catalase family. -
翻译后修饰
The N-terminus is blocked. -
细胞定位
Peroxisome. - Information by UniProt
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别名
- Cas1
- CAT
- CATA_HUMAN
see all
图片
数据表及文件
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SDS download
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Datasheet download
文献 (108)
ab83464 被引用在 108 文献中.
- Qiu L et al. Hydromorphone hydrochloride preconditioning combined with postconditioning attenuates myocardial ischemia/reperfusion injury in rats by improving mitochondrial function and activating the PI3K/Akt signaling pathway. Chem Biol Drug Des 103:e14474 (2024). PubMed: 38342769
- Sun TB et al. Hyperbaric oxygen therapy suppresses hypoxia and reoxygenation injury to retinal pigment epithelial cells through activating peroxisome proliferator activator receptor-alpha signalling. J Cell Mol Med 27:3189-3201 (2023). PubMed: 37731202
- Wang M et al. The SGK3-Catalase antioxidant signaling axis drives cervical cancer growth and therapy resistance. Redox Biol 67:102931 (2023). PubMed: 37866161
- Rahmani AH et al. Quercetin, a Plant Flavonol Attenuates Diabetic Complications, Renal Tissue Damage, Renal Oxidative Stress and Inflammation in Streptozotocin-Induced Diabetic Rats. Metabolites 13:N/A (2023). PubMed: 36677055
- Suraweera TL et al. Genistein and Procyanidin B2 Reduce Carcinogen-Induced Reactive Oxygen Species and DNA Damage through the Activation of Nrf2/ARE Cell Signaling in Bronchial Epithelial Cells In Vitro. Int J Mol Sci 24:N/A (2023). PubMed: 36835090