FOR RESEARCH USE ONLY |
Drug Names
Generic Name:CPV ELISA Kit.
Purpose
This kit allows for the determination of CPV concentrations in canine serum, and other biological fluids.
Principle of the assay
The kit assay CPV level in the sample,use Purified CPV antibody to coat microtiter plate wells, make solid-phase antibody, then add CPV to wells, Combined With CPV, after washing and removing non-combinative antibody and other components ,then Combined CPV antibody which with HRP labeled become antibody - antigen - enzyme-antibody complex, after washing Completely, Add TMB substrate solution,, TMB substrate becomes blue color At HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. Compared with the CUTOFF value, according to this to judge CPV exist in the sample or not.
Materials provided with the kit
Materials provided with the kit |
48determinations |
96 determinations |
Storage |
User manual |
1 |
1 |
|
Closure plate membrane |
2 |
2 |
|
Sealed bags |
1 |
1 |
|
Microelisa stripplate |
1 |
1 |
2 |
Negative control |
0.5ml×1 bottle |
0.5ml×1 bottle |
2 |
Positive control |
0.5ml×1 bottle |
0.5ml×1 bottle |
2 |
HRP-Conjugate reagent |
3ml×1 bottle |
6ml×1 bottle |
2 |
Sample diluent |
3ml×1 bottle |
6ml×1 bottle |
2 |
Chromogen Solution A |
3ml×1 bottle |
6ml×1 bottle |
2 |
Chromogen Solution B |
3ml×1 bottle |
6ml×1 bottle |
2 |
Stop Solution |
3ml×1 bottle |
6ml×1 bottle |
2 |
wash solution |
(20ml×20 fold) ×1bottle |
(20ml×30 fold) ×1bottle |
2 |
Specimen requirements
1. serum- coagulation at room temperature 10-20 mins,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.
2. plasma-use suited EDTA or citrate plasma as an anticoagulant,mix 10-20 mins ,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.
3. Urine-collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again. The Operation of Hydrothorax and cerebrospinal fluid Reference to it.
4. cell culture supernatant-detect secretory components, collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant,detect the composition of cells, Dilut cell suspension with PBS(PH7.2-7.4), Cell concentration reached 1 million / ml, repeated freeze-thaw cycles, damage cells and release of intracellular components, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.
5. Tissue samples- After cutting samples, check the weight,add PBS(PH7.2-7.4), Rapidly frozen with liquid nitrogen, maintain samples at 2 地 址: 上海市杨浦区政悦路88弄15号 联系人: 陈锋 电 话: 86-021-31665985 传 真: 86-021-51862175 Email:fd6218@sina.com
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