- ￥2890
- LSM Bio
- 0.156-10ng/ML
- 0.078 ng/Ml
- 进口
- ELI-36645h
- 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：
50
- 供应商：
LSMBIO
- 检测范围：
0.156-10ng/ML
- 检测方法：
夹心法
- 应用：
夹心法/竞争法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 Muscular LMNA-interacting protein,MLIP
- 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 Muscular LMNA- interacting protein, MLIP ELISA KIT
Product Name:Human Muscular LMNA- interacting protein, MLIP ELISA KIT
Packing:96T
Catalog No.:ELI-36645h
Gene Name:MLIP
Detect Range:78-5000 pg/mL
Sensitivity:32pg/mL
Target Protein Name:Muscular LMNA-interacting protein(MLIP
Alternative Name:MLIP,Muscular LMNA-interacting protein(MLIP
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Human Muscular LMNA- interacting protein, MLIP ELISA KIT allows for the in vitro quantitative determination of Muscular LMNA-interacting protein(MLIP concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Human Muscular LMNA- interacting protein, MLIP ELISA KIT has been pre-coated with an Muscular LMNA-interacting protein(MLIP antibody specific to Muscular LMNA-interacting protein(MLIP .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Muscular LMNA-interacting protein(MLIP 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 Muscular LMNA-interacting protein(MLIP, 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 Muscular LMNA-interacting protein(MLIP 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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文献和实验Use of Animal Models to Understand Human Muscular Dystrophy
In the decade following the identification of mutations in the dystrophin genein Duchenne (1 ) and Becker (2 ) muscular dystrophies (DMD/BMD), defects in components of the dystrophin-glycoprotein complex (DGC), which links F-
Interaction Trap/Two‐Hybrid System to Identify Interacting Proteins
pentagon, bait protein; open rectangle, noninteracting library protein; shaded box, activator protein (acid blob in Fig. ); open chevron, interacting library protein. View Image
Options for Development of Gene-Based Therapy for Muscular Dystrophy
The gene involved in Duchenne and Becker muscular dystrophies (DMD/ BMD) was the first human gene to be successfully identified by the approach of reverse genetics, or positional cloning (1 ), leading to the recognition of this approach
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