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- 详细信息
- 文献和实验
- 技术资料
- 库存:
20
- 供应商:
LSM BIO
- 检测范围:
78-5000pg/ml
- 检测方法:
夹心法ELISA或竞争法ELISA
- 应用:
检测小鼠血清,血浆,组织匀浆内的目标蛋白Presenilin-2, Psen2含量
- 适应物种:
小鼠
- 标记物:
Presenilin-2, Psen2
- 样本:
小鼠血清,血浆,组织匀浆及其他生物样本
- 灵敏度:
39pg/ml
- 规格:
96Tests
Mouse Presenilin-2, Psen2 ELISA试剂盒
Product Name: Mouse Presenilin-2, Psen2 ELISA试剂盒
Product Name: Mouse Presenilin-2, Psen2 ELISA试剂盒
Gene Name: Mouse Presenilin-2, Psen2
Detect Range:78-5000pg/ml
Sensitivity:39pg/ml
Target Protein Name: Mouse Presenilin-2, Psen2
Alternative Name: Mouse Presenilin-2, Psen2
ELISA type:Sandwich ELISA Kit
ELISA Test Principle:
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
Product Description: Mouse Presenilin-2, Psen2 ELISA试剂盒 allows for the in vitro quantitative determination of Mouse Presenilin-2, Psen2 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
The microtiter plate provided in Mouse Presenilin-2, Psen2 ELISA试剂盒 has been pre-coated with an Mouse Presenilin-2, Psen2 antibody specific to Mouse Presenilin-2, Psen2 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Presenilin-2, Psen2 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 Presenilin-2, Psen2 , 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 Presenilin-2, Psen2 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Apoptotic Proteolytic Cleavage of the Presenilins by Caspases
Familial Alzheimer’s disease (FAD) is a genetically heterogeneous disorder that is caused by defects in at least three early onset genes (age of onset:PS2 ) on chromosome 1 (1 ), presenilin 1 (PS1 ) on chromosome 14 (2 ), and amyloid protein
Quantifying Aβ1–40 and Aβ1–42 Using Sandwich-ELISA
with autosomal penetrance (reviewed in ref . 1 ). Several of these FAD-associated APP mutations, as well as FAD-associated mutations in the presenilin 1 (PS1) and presenilin 2 (PS2) genes, lead to an increase in the production of Aβ1 –42 relative to Aβ1 _40
Clinical Chemistry and Other Laboratory Tests on Mouse Plasma or Serum
Materials Lyophilized rat/mouse PINP calibrators 0 to 5 and controls 1 and 2 (from Competitive ELISA kit; IDS Ltd, http://www.idsplc.com/): reconstitute calibrators
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