ELISA Kit for Gastrin Releasing Peptide (GRP)
BN; GRP10; Bombesin; Neuromedin C
- Product No.UCEC506Mu
- Organism SpeciesMus musculus (Mouse) Same name, Different species.
- Test MethodCompetitive Inhibition
- Assay Length2h
- Detection Range12.35-1,000pg/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 5.15pg/mL.
- Sample Typeserum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
- Download Instruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
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FOB
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For more details, please contact local distributors!US$
For more details, please contact local distributors! US$
For more details, please contact local distributors! US$
For more details, please contact local distributors! US$
For more details, please contact local distributors!
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Packages (Simulation)
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Packages (Simulation)
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Results demonstration
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Typical Standard Curve
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ISO9001: 2008, ISO13485: 2003 Registered
Specificity of the ELISA Kit for Gastrin Releasing Peptide (GRP)
This assay has high sensitivity and excellent specificity for detection of Gastrin Releasing Peptide (GRP).
No significant cross-reactivity or interference between Gastrin Releasing Peptide (GRP) and analogues was observed.
Recovery of the ELISA Kit for Gastrin Releasing Peptide (GRP)
Matrices listed below were spiked with certain level of recombinant Gastrin Releasing Peptide (GRP) and the recovery rates were calculated by comparing the measured value to the expected amount of Gastrin Releasing Peptide (GRP) in samples.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 80-99 | 90 |
| EDTA plasma(n=5) | 81-88 | 85 |
| heparin plasma(n=5) | 89-104 | 93 |
Precision of the ELISA Kit for Gastrin Releasing Peptide (GRP)
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Gastrin Releasing Peptide (GRP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Gastrin Releasing Peptide (GRP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
Linearity of the ELISA Kit for Gastrin Releasing Peptide (GRP)
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Gastrin Releasing Peptide (GRP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 80-96% | 79-93% | 80-91% | 98-105% |
| EDTA plasma(n=5) | 87-103% | 94-105% | 95-103% | 90-104% |
| heparin plasma(n=5) | 81-93% | 82-89% | 91-101% | 85-94% |
Stability of the ELISA Kit for Gastrin Releasing Peptide (GRP)
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.
Assay procedure summary of the ELISA Kit for Gastrin Releasing Peptide (GRP)
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.
Test principle of the ELISA Kit for Gastrin Releasing Peptide (GRP)
This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to GRP has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled GRP and unlabeled GRP (Standards or samples) with the pre-coated antibody specific to GRP. 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 GRP in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of GRP in the sample.
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