- ￥2890
- LSM Bio
- 0.156-10ng/ML
- 0.078 ng/Ml
- 进口
- ELI-45084h
- 2025年07月12日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
20
- 供应商：
LSMBIO
- 检测范围：
0.156-10ng/ML
- 检测方法：
夹心法
- 应用：
夹心法ELISA体外定量检测人血清、血浆或其它相关生物液体中蛋白浓度
- 适应物种：
人
- 标记物：
Human Primary ciliary dyskinesia protein 1,PCDP1
- 样本：
人血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度：
0.078 ng/Ml
- 规格：
96T
Human Primary ciliary dyskinesia protein 1,PCDP1 ELISA KIT
Product Name:Human Primary ciliary dyskinesia protein 1,PCDP1 ELISA KIT
Packing:96T
Catalog No.:Human PCDP1 ELISA KIT
Gene Name:PCDP1
Detect Range:0.312-20 ng/mL
Sensitivity:0.039ng/mL
Target Protein Name:Human PCDP1
Alternative Name:Human PCDP1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human PCDP1 ELISA KIT allows for the in vitro quantitative determination of Human PCDP1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human PCDP1 ELISA KIT has been pre-coated with an Human PCDP1 antibody specific to Human PCDP1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Human PCDP1 and then 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 Human PCDP1, 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.The concentration of Human PCDP1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
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will focus on measurements of cytoplasmic and mitochondrial Ca2+ signals resulting from GPCR activation in polarized primary cultures of normal and CF human bronchial epithelia (HBE).
Assessing PCP in the Cochlea of Mammalian Ciliopathy Models
Biedl Syndrome, Primary Ciliary Dyskinesia, and Polycystic Kidney Disease, among many others. In mouse models of Alstr�m Syndrome and Bardet–Biedl Syndrome, we have shown developmental defects in the mechano-sensory stereociliary bundles on the apical
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