- ￥3861 - 5499
- Biorbyt
- 0.16-10 ng/mL
- 0.057 ng/mL
- orb781444
- 英国
- 2026年08月04日
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- 文献和实验
- 技术资料
- 库存：
99
- 供应商：
Biorbyt
- 检测范围：
0.16-10 ng/mL
- 检测方法：
Sandwich
- 应用：
ELISA
- 适应物种：
Human
- 样本：
tissue homogenates, cell lysates and other biological fluids
- 灵敏度：
0.057 ng/mL
- 规格：
48 T/96 T
| 规格： | 48 T | 产品价格： | ￥3861.0 |
|---|---|---|---|
| 规格： | 96 T | 产品价格： | ￥5499.0 |
描述: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Specificity Protein 1(Sp1).
别名: TSFP1 ELISA Kit, Sp1 Transcription Factor ELISA Kit
浓度: 10 ng/mL
应用说明: standard: 10 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human Sp1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human Sp1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human Sp1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human Sp1 in the samples is then determined by comparing the OD of the samples to the standard curve
检测时间: 3.5h
研究领域: Signal Transduction
备注: For research use only.
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文献和实验Specificity Profiling of Protein‐Binding Domains Using One‐Bead‐One‐Compound Peptide Libraries
against macromolecular targets. They have proven particularly useful in profiling the binding specificity of protein modular domains (e.g., SH2 domains, BIR domains, and PDZ domains); subsequently, the specificity information can be used to predict the protein targets
ELISA原理与实验方法The advantages of the ELISA are similar to other antibody-labeled reactions which include specificity, sensitivity, inexpensiveness, and safety. Since the enzyme label is the critical portion of ELISA, its selection is very important
Mapping Protein‐Protein Interactions with Phage‐Displayed Combinatorial Peptide Libraries
by purification of selected phage by ELISA. Alternatively, there is a bead?based affinity selection method. These methods allow one to readily isolate peptide ligands that bind to a protein target of interest and use the consensus sequence to search proteomic
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