- ￥2980
- LSM Bio
- 78-5000pg/ml
- 46.9pg/ml
- 进口
- ELA-E0296r
- 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 Lactoperoxidase,LPO
- 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 Lactoperoxidase, LPO ELISA Kit
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE
BEGINNING!
Synonyms
Lactoperoxidase(LPO),Salivary peroxidase(SPO), SAPX
Search name
RatLactoperoxidase ELISA Kit, RatLPO ELISA Kit, RatSalivary peroxidase ELISA Kit, RatSPO ELISA Kit,
RatSAPX ELISA Kit,
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Ratlactoperoxidase,LPO 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 LPO. Standards or samples are then added to the
appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for LPO 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 LPO, 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 LPO 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
本法反应温和，对抗原、抗体免疫活性影响小，已被广泛应用。缺点是标记率较低，一般为20～40%。 1．原理此法是利用乳过氧化物酶（Lactoperoxidase）有促进微量过氧化氢对125I-的氧化作用，生成125I+，并标记在多肽、蛋白质酪氨酸分子上。 2．方法以标记蛋白质抗原为例。 （1）反应液组成：蛋白质2～5μg溶于磷酸缓冲液10～25μl中，加入Na125i 1m Ci(10μl)、乳过氧化物酶溶液25ng(10μl)、H2O2200ng(10μl
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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