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- 详细信息
- 文献和实验
- 技术资料
- 库存:
50
- 供应商:
LSM BIO
- 检测范围:
78-5000pg/ml
- 检测方法:
夹心法ELISA
- 应用:
检测小鼠血清,血浆,组织匀浆内的目标蛋白含量
- 适应物种:
小鼠
- 标记物:
Gap junction delta-2 protein, Gjd2
- 样本:
小鼠血清,血浆,组织匀浆
- 灵敏度:
39pg/ml
- 规格:
96Tests
Mouse Gap junction delta- 2 protein, Gjd2 ELISA KIT
Product Name:Mouse Gap junction delta- 2 protein, Gjd2 ELISA KIT
Packing:96T
Catalog No.:ELI-47391m
Gene Name:Mouse Gjd2
Detect Range:15.6-1000pg/ml
Sensitivity:9.375pg/ml
Target Protein Name:Mouse Gjd2
Alternative Name:Mouse Gap junction delta-2 protein, Gjd2
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Gap junction delta- 2 protein, Gjd2 ELISA KIT allows for the in vitro quantitative determination of Mouse Gjd2 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Gap junction delta- 2 protein, Gjd2 ELISA KIT has been pre-coated with an Mouse Gap junction delta-2 protein, Gjd2 antibody specific to Mouse Gjd2 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Gjd2 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 Mouse Gjd2 , 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 Mouse Gjd2 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Functional Stem Cell Integration Assessed by Organotypic Slice Cultures
neural stem cells (NSCs) filled with the gap junction‐permeable dye calcein (green) and the gap junction‐impermeable dye DiI (red) following engraftment to an organotypic striatal tissue culture. Cell nuclei are displayed by DAPI nuclear counterstain
Ex Ovo Electroporation of DNA Vectors into Pre-gastrulation Avian Embryos
as stage X, nearly 24 h earlier in development than most electroporation protocols. Compared to in ovo electroporation, the ex ovo method allows easier embryo orientation (the posterior half of the embryo is darker than the anterior half
【转帖】Top 100 proteomics publications
Technol Biomed Life Sci 20. Chung et al. (2006) Genomics and proteomics: Emerging technologies in clinical cancer research. Crit Rev Oncol Hematol 21. Kislinger et al. (2006) Global survey of organ and organelle protein expression in mouse
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