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BioAssay Systems/EnzyChrom™ Catalase Assay Kit/100 tests/ECAT-100
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4000-520-616
EnzyChrom™ Catalase Assay Kit
- Product Overview
- Product FAQ
- Product Citations
- Assay Service
ProtocolSDS
Application
- For quantitative determination of catalase activity and evaluation of drug effects on catalase activity.
Key Features
- Sensitive and accurate. Use 10 μL sample. Linear detection range 0.2 to 5 U/L catalase activity.
- Simple and Convenient. The procedure involves adding a Substrate to sample, incubation for 30 min, followed by a Detection Reagent and reading the optical density or fluorescence intensity.
Method
- OD570nm, or FL530/585nm
Samples
- Serum, plasma, urine, saliva, cell culture etc
Species
- All
Size
- 100 tests
Detection Limit
- 0.2 U/L
Shelf Life
- 6 months
More Details
- CATALASE (EC 1.11.1.6), is an ubiquitous antioxidant enzyme that catalyzes the decomposition of hydrogen peroxide (H2O2) to water and oxygen. By preventing excessive H2O2 build up, catalase allows important cellular processes which produce H2O2 as a byproduct to occur safely. Deficiency in catalase activity has been associated with grey hair and peroxisomal disorder acatalasia. Simple, direct and high-throughput assays for catalase activity find wide applications. BioAssay Systems improved assay directly measures catalase degradation of H2O2 using a redox dye. The change in color intensity at 570nm or fluorescence intensity (λex/em = 530/585nm) is directly proportional to the catalase activity in the sample.
Regarding the technique used in the DPOD-100 peroxidase assay and the ECAT-100 catalase assay that seems to be really similar, how will we be sure that one of them will measure the catalase activity and the other the peroxidase?
The DPOD assay measures the conversion of the dye reagent and hydrogen peroxide, which are provided in large excess as substrates for cellular peroxidases. Endogenous catalase activity does not interfere with the assay, because it does not react with the dye reagent, hydrogen peroxide is in large excess, and the reaction is short (10 minutes), leaving the H2O2 concentration practically unchanged.The ECAT assays measures catalase activity by first incubating much lower concentrations of hydrogen peroxide with the samples for 30 minutes. Then the decrease in hydrogen peroxide is measured by adding the dye reagent and HRP in excess.You will have 100 µL of each standard when you have pipetted all solutions for the standard curve. How stable are the 100 µl standards? Can they be used the next day to make another standard curve or can the values from the already made standard curve be used when you have other samples the next day?
The H2O2 standards are stable for an hour. Therefore assays should be run as soon as possible with the samples and standards. It is recommended that customers run standard curve in each experiment.For more detailed product information and questions, please feel free to Contact Us. Or for more general information regarding our assays, please refer to our General Questions.Lin, Ting-An, et al (2019). Red Quinoa Bran Extracts Protects against Carbon Tetrachloride-Induced Liver Injury and Fibrosis in Mice via Activation of Antioxidative Enzyme Systems and Blocking TGF-beta1 Pathway. Nutrients 11.2: 395. Assay: Catalase in mice liver tissue. Cueno, Marni E., and Kuniyasu Ochiai (2018). Gingival periodontal disease (PD) level-butyric acid affects the systemic blood and brain organ: insights into the systemic inflammation of periodontal disease. Frontiers in immunology 9:1158. Assay: Catalase in rat blood cytosol. Kang, Changwoo, et al (2018). Therapeutic effect of ascorbic acid on dapsone-induced methemoglobinemia in rats. Clinical and experimental emergency medicine 5.3: 192. Assay: Catalase in rat plasma. Salvatori, Ornella, et al (2018). Candida albicans Ras1 inactivation increases resistance to phagosomal killing by human neutrophils. Infection and immunity 86.12: e00685-18. Assay: Catalase in Candida albicans cells. Camini, Fernanda Caetano, et al (2017). Oxidative stress in Mayaro virus infection. Virus research 236: 1-8. Assay: Catalase in human cells. Kang, Hyeon Hui, et al (2017). Chronic intermittent hypoxia induces liver fibrosis in mice with diet-induced obesity via TLR4/MyD88/MAPK/NF-kB signaling pathways. Biochemical and biophysical research communications 490.2: 349-355. Assay: Catalase in mice tissues. Kook, Sung-Ho, et al (2017). Dietary hydroxycinnamates prevent oxidative damages to liver, spleen, and bone marrow cells in irradiation-exposed mice. Food science and biotechnology 26.1: 279-285. Assay: Catalase in mice tissues. Oliveira, C. S., et al (2017). Moderate aerobic exercise on the recovery phase of gentamicin-induced acute kidney injury in rats. Life sciences 169: 37-42. Assay: Catalase in rat tissues. Pradhan, Arnab, et al (2017). Elevated catalase expression in a fungal pathogen is a double-edged sword of iron. PLoS pathogens 13.5: e1006405. Assay: Catalase in C. albicans cells. Cueno ME (2013). Orally supplemented catechin increases heme amounts and catalase activities in rat heart blood mitochondria: a comparison between middle-aged and young rats. Exp Gerontol. 48(11):1319-22. Assay: Catalase in rat blood mitochondria. Chiu CC et al (2012). Beneficial Effects of Ocimum gratissimum Aqueous Extract on rats with CCl(4)-Induced Acute Liver Injury. Evid Based Complement Alternat Med 2012:736752. Assay: Catalase in rat serum. Hadzi-Petrushev N et al (2012). L-2-oxothiazolidine-4-carboxylate influence on age- and heat exposure-dependent peroxidation in rat"s liver and kidney. J Therm Biol 37(5):361-365. Assay: Catalase in rat Kidney. Hadzi-Petrushev N et al (2012). L-2-oxothiazolidine-4-carboxylate influence on age- and heat exposure-dependent peroxidation in rat"s liver and kidney. J Therm Biol 37(5):361-365. Assay: Catalase in rat Kidney.Zhu T et al (2012) Effects of the iron-chelating agent deferoxamine on triethylene glycol dimethacrylate, 2-hydroxylethyl methacrylate, hydrogen peroxide-induced cytotoxicity. J Biomed Mater Res B Appl Biomater 100(1):197-205. Assay: Catalase in human dental pulp cells. Hadzi-Petrushev N et al (2011) L-2-oxothiazolidine-4-carboxylate influence on age- and heat exposure-dependent redox changes in rat"s blood plasma. J Physiol Sci 61(5):437-442. Assay: Catalase in rat plasma. Labib, HM, et al (2010). The Role of Oxidative Stress Markers and Nitric Oxide Levels in the Pathogenesis of Glaucoma. Austr. J. Basic and Applied Sci 4(8): 3553-3558. Assay: Catalase in human blood. To find more recent publications, pleaseclick here.
If you or your labs do not have the equipment or scientists necessary to run this assay, BioAssay Systems can perform the service for you.Simply send us your samples:- Fast turnaround - Quality data - Low costPlease email or call 1-510-782-9988 x 2 to request assay service.
蚂蚁淘电商平台
ebiomall.com
ebiomall.com
公司简介
蚂蚁淘(www.ebiomall.cn)是中国大陆目前唯一的生物医疗科研用品B2B跨境交易平台,
该平台由多位经验丰富的生物人和IT人负责运营。蚂蚁淘B2B模式是指客户有采购意向后在蚂蚁
淘搜索全球供应信息,找到合适的产品后在蚂蚁淘下单,然后蚂蚁淘的海外买手进行跨境采购、
运输到中国口岸,最后由蚂蚁淘国内团队报关运输给客户...
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蚂蚁淘所有产品都是自运营的,我们已经跟国外多家厂方建立品牌推广合作关系, 获得对方的支持和授权; 同时客户可以通过订单详情查看到货物从厂方至客户的所有流程, 确保货物的来源; 正规报关,提供13%增值税发票。
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轻松采购: 在线下单 简单省事
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2018-12-26
分析色谱是制备色谱的基础。当我们在分析色谱上 取得了良好的分离效果时,可以将其放大,应用到制备色谱上,由此,我们需要考虑调整上样量,流速,梯度:1.上样量的调整:他与分析色谱柱和制备色谱柱的柱长和柱内径有关:具体关系时;制备柱上样量/分析柱上样量=制备猪场/分析柱长*制备柱内径 查看更多
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Western免疫印迹(Western Blot)是将蛋白质转移到膜上,然后利用抗体进行检测。对已知表达蛋白,可用相应抗体作为一抗进行检测,对新基因的表达产物,可通过融合部分的抗体检测。原理与Sou 查看更多
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摘要:本文主要是针对Western bloting的原理及操作进行了简单的阐述,Western印迹法是利用抗原抗体的免疫反应,先将蛋白通过SDS-PAGE电泳分离开来,然后再利用电场力的作用将胶上的蛋白转移到 查看更多
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常见问题
蚂蚁淘所售产品均为正品吗?
蚂蚁淘的创始人兼CEO是钟定松先生,具有十年的从业经验,在业界享有良好的口碑;
Ebiomall是跨境直采平台,我们直接从厂家采购,自己的团队负责国际物流和清关,中间没有第三方,蚂蚁淘承诺所售产品仅为正品,假一罚十。
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商品咨询
在什么情况下要做免疫组化区分胰腺癌和胰腺_有问必答_123
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免疫组化在临床工作的意义近年来,随着免疫组织化学技术的发展和各种特异性抗体的出现,使许多疑难肿瘤得到了明确诊断。在常规肿瘤病理诊断中,5%-10%的病例单靠H.E.染色难以作出明确的形态学诊断。尤其是免疫组化在肿瘤诊断和鉴别诊断中的实用价值受到了普遍的认可,其在低分化或未分化肿瘤的鉴别诊断时,准确率可达50%-75%。免疫组织化学的临床应用主要包括以下几方面:(1)恶性肿瘤的诊断与鉴别诊断;(2)确定转移性恶性肿瘤的原发部位;(3)对某类肿瘤进行进一步的病理分型;(4)软组织肿瘤的治疗一般需根据正确的组织学分类,因其种类多、组织形态相像,有时难以区分其组织来源,应用多种标志进行免疫组化研究对软组织肿瘤的诊断是不可缺少的;(5)发现微小转移灶,有助于临床治疗方案的确定,包括手术范围的确定。(6)为临床提供治疗方案的选择。
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我打算从中山公司定SANTACRUZ公司的mmp-9抗体,但是听师姐说这个公司
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