提供者：上海杏宜生物科技有限公司 发布时间：2021/9/15 14:30:17 阅读次数：208次 进入该公司店铺
(PPAR-α)ELISA Kit
l Forresearchuseonly.
l For the quantitative in vitro determination ofPPAR-αconcentrations in Mouse serum, plasma, culture media or any biological fluid.
l Expiration date：six months .
l Storage： 2-8℃.
Principle
This ELISA kit uses Sandwich-ELISA as the method. The Microelisa stripplate provided in this kit has been pre-coated with an antibody specific toPPAR-α. Standards or samples are added to the appropriate Microelisa stripplate wells ａnd combined to the specific antibody. Then a Horseradish Peroxidase (HRP)- conjugated antibody specific for PPAR-αis added to each Microelisa stripplate well ａnd incubated. Free components are washed away. The TMB substrate solution is added to each well.Only those wells that contain PPAR-αand HRP conjugatedPPAR-αantibody will appear blue in color and then turn yellow after the addition of the s solution. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of PPAR-α,You can calculate the concentration of PPAR-α in the samples by comparing the OD of the samples to the standard curve.
Materials provided with the kit
Materials provided with the kit | 48 determinations | 96 determinations | Storage | |
1 | User manual | 1 | 1 | R.T. |
2 | Closure plate membrane | 2 | 2 | R.T. |
3 | Sealed bags | 1 | 1 | R.T. |
4 | Microelisa stripplate | 1 | 1 | 2-8℃ |
5 | Standard：2700 pg/ml | 0.5ml×1 bottle | 0.5ml×1 bottle | 2-8℃ |
6 | Standard diluent | 1.5ml×1 bottle | 1.5ml×1 bottle | 2-8℃ |
7 | HRP-Conjugate reagent | 3ml×1 bottle | 6ml×1 bottle | 2-8℃ |
8 | Sample diluent | 3ml×1 bottle | 6ml×1 bottle | 2-8℃ |
9 | Chromogen Solution A | 3ml×1 bottle | 6ml×1 bottle | 2-8℃ |
10 | Chromogen Solution B | 3ml×1 bottle | 6ml×1 bottle | 2-8℃ |
11 | S Solution | 3ml×1 bottle | 6ml×1 bottle | 2-8℃ |
12 | wash solution | 20ml(20X)×1bottle | 20ml(30X)×1bottle | 2-8℃ |
Sample preparation
1. Serum preparation
After collection of thewhole blood, allow the blood to clot by leaving it undisturbed at room temperature. This usually takes 10-20 minutes. Remove the clot by centrifuging at 2,000-3,000 rpm for 20 minutes.If precipitates appear during reservation, the sample should be centrifugated again.
2.Plasma preparation
Collect the whole blood into tubes with anticoagulant (EDTA or citrate). After incubated at room temperature for 10-20 minutes, tubes are centrifugated for 20 min at 2,000-3,000 rpm. Collect the supernatant carefully as plasma samples. If precipitates appear during reservation, the sample should be centrifugated again.
3. Urine samples
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