- ￥2980
- LSM Bio
- 78-5000pg/ml
- 46.9pg/ml
- 进口
- ELA-E0874r
- 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 Bradykinin
- 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 Bradykinin ELISA Kit
FOR RESEARCH USE ONLY!
96 Tests
Alternative name
Rat Bradykinin ELISA KIT ,Rat KNG1 ELISA KIT ,Rat BDK ELISA KIT ,Rat KNG ELISA KIT ,Rat kininogen-1 ELISA KIT ,Rat HMWK ELISA KIT ,Rat alpha-2-thiol proteinase inhibitor ELISA KIT ,Rat fitzgerald factor ELISA KIT ,Rat high molecular weight kininogen ELISA KIT ,Rat williams-Fitzgerald-Flaujeac factor ELISA KIT ,Rat kininogen 1 ELISA KIT
Intended use
Rat Bradykinin ELISA kit allows for the in vitro quantitative determination of Rat Bradykinin concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.
Test principle
Rat Bradykinin ELISA kit Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for Bradykinin 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 Bradykinin, 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 Bradykinin in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Rat Bradykinin ELISA kit Range 1.25-80ng/ml
Order Bradykinin ELISA kit by
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文献和实验上海西唐生物科技有限公司 021-55229872, 65333639 www.westang.com 大鼠缓激肽 (Bradykinin)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。用抗大鼠 Bradykinin 单抗包被于酶标板上，标准品和样品中的 Bradykinin 与单抗结合，加入生物素化的抗大
RAT/MOUSE GROWTH HORMONE ELISA KIT
实验原理 This assay is a Sandwich ELISA based, sequentially, on: 1) capture of rat or mouse Growth Hormone molecules from samples to the wells of a microtiter plate coated by a pre-titered amount of anti-Growth Hormone
at 4°C for 15 minutes. 9. Remove and aliquot supernatant. We recommend making several 50 μl aliquots. 10. Before running ELISA, dilute protein 1:100 and run a Bradford total protein assay or Quant-iT™ Protein Quantitation Kit assay (Cat. no. Q
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