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中文名称

Cholecystokinin 8, Octapeptide (CCK8) BioAssay ELISA Kit (Rat)

英文名字
Cholecystokinin 8, Octapeptide (CCK8) BioAssay ELISA Kit (Rat)
供应商
USBiological
产品货号
024110
产品报价
¥1/48Tests   ¥1/96Tests
产品说明书
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产品新闻
背景资料
USBiological品牌是全球有名的抗原抗体和生化试剂供应商,生产世界上种类最多的抗体,用于Western Blot、免疫沉淀、免疫荧光、免疫组化和流式细胞术等多种检测方法。武汉艾美捷科技作为USBiological品牌中国区域总代理,是行业中少有的致力于服务客户,帮助客户,且拥有独立的专业销售团队、技术支持团队、市场营销团队、进出口报关团队的高科技生物企业。可以为您提供及时的咨询响应,专业的产品和解决方案支持,稳健快捷的交货周期,优质放心的售后服务。我们致力于为您提供有价值的产品和服务,在意您的成功!
产品描述
The Rat Cholecystokinin 8, Octapeptide (CCK8) ELISA Kit is a competitive inhibition immunoassay for the in vitro quantitative measurement of CCK8in rat serum, plasma, tissue homogenates, cell lysates, cell culture supernatants and other biological fluids.Detection Range:12.35-1,000pg/mlSensitivity:<4.45pg/mlPrecision:Intra-Assay CV: <10%Inter-Assay CV: <12%Test Principle:This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific for CCK8 has been pre-coated onto a microplate. A competitive inhibition reaction occurs between biotin-labeled CCK8 and unlabeled CCK8 (standards or samples) for limited binding sites on the pre-coated antibody. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is inversely proportional to the concentration of CCK8 in the sample. After addition of the substrate solution, the intensity of color developed is inversely proportional to the concentration of CCK8 in the sample.Kit Components:*024110A: Microtiter Plate, 96 wells, Pre-coated, ready to use.*024110B: Standard, 2x1vial 024110C: Standard Diluent, 1x20ml*024110D: Detection Reagent A, 1x120ul *024110E: Detection Reagent B, 1x120ul 024110F: Assay Diluent A, 1x12ml024110G: Assay Diluent B, 1x12ml024110H: TMB Substrate, 1x9ml024110K: Stop Solution, 1x6ml024110L: Wash Buffer, 30X, 1x20ml024110M: Reagent Diluent, 1x300ulStorage and Stability:Store *024110A, *024110B, *024110D and *024110E at -20°C. Store all the other components at 4°C. Unused kit is stable for 6 months. Once kit components are opened, it is highly recommended to use remaining reagents within 1 month provided this is within the expiration date of the kit. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.Materials Required But Not Supplied:1. Microplate reader with 450 ± 10nm filter.2. Precision single or multi-channel pipettes and disposable tips.3. Eppendorf Tubes for diluting samples.4. Deionized or distilled water.5. Absorbent paper for blotting the microtiter plate.6. Container for Wash SolutionSample Preparation and Storage:Serum:Allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 20 minutes at approximately 1000xg. Assay freshly prepared serum immediately or store samples in aliquots at -20°C or -80°C for later use. Avoid repeated freeze/thaw cycles.Plasma:Collect plasma using EDTA or heparin as anticoagulant. Centrifuge samples for 15 minutes at 1000xg at 2-8° within 30 minutes of collection. Remove plasma and assay immediately or store samples in aliquots at -20°C or -80°C for later use. Avoid repeated freeze/thaw cycles.Tissue Homogenates:The preparation of tissue homogenates will vary depending upon tissue type. For this assay, tissues were rinsed thoroughly in ice-cold PBS (0.02M pH 7.0-7.2) to remove excess blood and weighed before homogenization. The tissues were minced to small pieces and homogenized in 5-10ml of PBS with a glass homogenizer on ice (Micro Tissue Grinders works too). The resulting suspension was sonicated with an ultrasonic cell disrupter or subjected to two freeze-thaw cycles to further break the cell membranes. After that, the homogenates were centrifuged for 5 minutes at 5000×g. The supernatant was removed and assayed immediately or aliquoted and stored at -20°C or lower.Cell Lysates: Cells must be lysed before assaying according to the following directions. 1. Adherent cells should be detached with trypsin and then collected by centrifugation (suspension cells can be collected by centrifugation directly). 2. Wash cells three times in cold PBS. 3. Resuspend cells in PBS (1×) and subject the cells to ultrasonication 4X (or freeze cells at -20°C. Thaw cells with gentle mixing. Repeat the freeze/thaw cycle 3X.) 4. Centrifuge at 1500×g for 10 minutes at 2-8°C to remove cellular debris.Cell Culture Supernatants and Other Biological Fluids:Centrifuge samples for 20 minutes at 1000×g. Remove particulates and assay immediately or store samples in aliquots at -20°C or -80°C. Avoid repeated freeze/thaw cycles.Assay Procedure Summary:1. Prepare all reagents, samples and standards.2. Add 50ul standard or sample to each well, then add 50ul prepared Detection Reagent A immediately. Shake and mix. Incubate 1 hour at 37°C.3. Aspirate and wash 3 times.4. Add 100ul prepared Detection Reagent B. Incubate 30 minutes at 37°C.5. Aspirate and wash 5 times.6. Add 90ul Substrate Solution. Incubate 15-25 minutes at 37°C.7. Add 50ul Stop Solution. Read absorbance at 450nm immediately.
产品特点
针对Cholecystokinin 8, Octapeptide (CCK8) BioAssay ELISA Kit (Rat)该产品的特点优势,欢迎查阅官网提供的产品说明书。
保存建议
建议收到Cholecystokinin 8, Octapeptide (CCK8) BioAssay ELISA Kit (Rat)产品后将其置于4°C/-20°C保存。
其他
Usbiological公司是美国著名的抗体和生化试剂供应商,生产世界上种类最多的抗体,用于Western Blot、免疫沉淀、免疫荧光、免疫组化和流式细胞术等多种检测方法。Usbiological公司现已拥有超过50,19234种抗体、抗原和生化产品,为科研用户提供了诸多超值选择。
注意
该页面的中文产品信息的翻译,仅供参考。准确的产品信息请以厂家的英文说明书为准。下单前,请浏览说明书确认。
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