ELISA Kit for Prostaglandin E2 (PGE2)
Product Code:
CEA538Ge
CEA538Ge
Regulatory Status:
RUO
RUO
Target Species:
Species Independent
Species Independent
Application:
Enzyme-Linked Immunosorbent Assay (ELISA)
Enzyme-Linked Immunosorbent Assay (ELISA)
No additional charges, what you see is what you pay! *
| Code | Size | Price |
|---|
| CEA538Ge-24T | 24T | £242.00 |
Quantity:
| CEA538Ge-48T | 48T | £401.00 |
Quantity:
| CEA538Ge-96T | 96T | £560.00 |
Quantity:
| CEA538Ge-96T*5 | 96T*5 | £2,413.00 |
Quantity:
| CEA538Ge-96T*10 | 96T*10 | £4,530.00 |
Quantity:
Prices exclude any Taxes / VAT
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: China.
Typical lead time: 14-21 working days.
Contact us for more accurate information.
Typical lead time: 14-21 working days.
Contact us for more accurate information.
- Further Information
- Documents
- References
- Show All
Further Information
Alternative Names:
PG-E2
Assay length:
2h
Assay Procedure Summary:
1. Prepare all reagents, samples and standards;
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 50µL Stop Solution. Read at 450 nm immediately.
2. Add 50µL standard or sample to each well.
And then add 50µL prepared Detection Reagent A immediately.
Shake and mix. Incubate 1 hour at 37°C;
3. Aspirate and wash 3 times;
4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
5. Aspirate and wash 5 times;
6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
7. Add 50µL Stop Solution. Read at 450 nm immediately.
Detection range:
2.47-200pg/mL
Format:
48T, 96T, 96T?5, 96T?10, 96T?100
Item Name:
Prostaglandin E2
Method:
Competitive Inhibition
Precision:
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Prostaglandin E2 (PGE2) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Prostaglandin E2 (PGE2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Prostaglandin E2 (PGE2) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Research Area:
Metabolic pathway;Infection immunity;Endocrinology;Hormone metabolism;
Sample type:
Serum, plasma and other biological fluids
Sensitivity:
The minimum detectable dose of this kit is typically less than 0.92pg/mL
Specificity:
This assay has high sensitivity and excellent specificity for detection of Prostaglandin E2 (PGE2).
No significant cross-reactivity or interference between Prostaglandin E2 (PGE2) and analogues was observed.
No significant cross-reactivity or interference between Prostaglandin E2 (PGE2) and analogues was observed.
Stability:
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Test Principle:
This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to PGE2 has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled PGE2 analogues and unlabeled antigen (Standards or samples) with the pre-coated antibody. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of PGE2 in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of PGE2 in the sample.
References
http://www.ncbi.nlm.nih.gov/pubmed/20969848; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724827/; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557222/; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3378786/; http://www.ncbi.nlm.nih.gov/pubmed/24446394; http://www.ncbi.nlm.nih.gov/pubmed/24211397; http://www.ncbi.nlm.nih.gov/pubmed/24948542; http://www.ncbi.nlm.nih.gov/pubmed/24962643; http://www.ncbi.nlm.nih.gov/pubmed/24909904; http://www.ncbi.nlm.nih.gov/pubmed/25777539; http://www.ncbi.nlm.nih.gov/pubmed/26407653; http://www.ncbi.nlm.nih.gov/pubmed/26632817 ; www.ncbi.nlm.nih.gov/pubmed/25982596; www.ncbi.nlm.nih.gov/pubmed/26677041; www.ncbi.nlm.nih.gov/pubmed/25719613; www.ncbi.nlm.nih.gov/pubmed/25575733; http://www.ncbi.nlm.nih.gov/pubmed/27230680; http://www.ncbi.nlm.nih.gov/pubmed/27058422; http://www.ncbi.nlm.nih.gov/pubmed/27056726; https://www.ncbi.nlm.nih.gov/pubmed/27058422; https://www.ncbi.nlm.nih.gov/pubmed/27747453