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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 Podocin,Nphs2
- 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 Podocin, NPHS2 ELISA KIT
96 Tests
Operating instruction
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!
Synonyms
Podocin, NPHS2,nephrosis 2, idiopathic, steroid-resistant (podocin); podocin; PDCN; SRN1
Search name
Rat Podocin ELISA KIT ,Rat NPHS2 ELISA KIT ,Rat nephrosis 2 ELISA KIT ,Rat idiopathic ELISA KIT ,Rat steroid-resistant ELISA KIT ,Rat podocin ELISA KIT ,Rat PDCN ELISA KIT ,Rat SRN1 ELISA KIT
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Rat Podocin 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 Podocin. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for Podocin 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 Podocin, 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 Podocin in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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文献和实验原因。这篇文章旨在探索用 AAV 基因疗法治疗由 NPHS2 基因突变引起的肾病综合征。 实验设计 AAV-LK03 和 AAV 2/9 的选择:研究者比较了 AAV-LK03 和 AAV 2/9 两种血清型在人类和鼠类足细胞中的转导效率。 体外实验:通过体外培养的突变人类足细胞中来测试基因疗法的效果。 体内实验:在诱导型足细胞蛋白(Podocin)敲除小鼠模型中测试疾病诱导前(预防性)的基因治疗效果,在诱导型突变 Podocin 敲入小鼠中测试疾病诱导后(治疗性)的基因疗法效果。 图 4 体内
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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