- ￥2980
- LSM Bio
- 78-5000pg/ml
- 46.9pg/ml
- 进口
- ELA-E0110r
- 2025年07月16日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
LSM BIO
- 检测范围：
78-5000pg/ml
- 检测方法：
夹心法
- 应用：
检测大鼠血清、血浆或其它相关生物液体中天然和重组蛋白
- 适应物种：
大鼠
- 标记物：
Rat Oncostatin-M
- 样本：
大鼠血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度：
46.9pg/ml
- 规格：
96tests
Rat Oncostatin-M,OSM ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
Oncostatin-M(OSM),;
Search name
Rat OSM ELISA KIT ,Rat oncostatin M ELISA KIT ,Rat Oncostatin-M ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of rat oncostatin-m,OSM concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Test principle
The microtiter plate provided in this kit has been pre-coated with an antibody specific to OSM. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for OSM and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain OSM, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of OSM in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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文献和实验人载脂蛋白M (APO M)ELISA 试剂盒 ( 用于血清、血浆、细胞培养上清液和其它生物体液内 ) 原理 本实验采用双抗体夹心 ABC-ELISA 法。用抗人 APO M 单抗包被于酶标板上，标准品和样品中的 APO M与单抗结合，加入生物素化的抗人 APO M ，形成免疫复合物连接在板上，辣根
R&DSystems总公司于1976年成立于美国，在美国NASDAQ上市(TECH)。公司一直致力于各种细胞因子及其相关分子的生产研发。R&D Systems产品覆盖面广，种类丰富，质量稳定可靠，其生产的各种ELISA试剂盒、重组因子及抗体以其卓越的品质赢得了世界各国科研及临床诊断机构的青睐。 公司网址：www.RnDSystemsChina.com.cn
developed for in vitro studies (4 ). Recently, we have refined this approach to apply to in vivo studies of acute CNS injury (5 ,6 ). This technique allows for differential and concurrent measurement of the two major isoforms of calpain, m-calpain and μ
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