Mouse ELISA Kits

Home / Products / Traditional ELISA / Mouse ELISA Kits
Mouse RAPGEF2(Rap Guanine Nucleotide Exchange Factor 2) ELISA Kit
Copy Product Information

Product No

FY-EM5505

Sample Type

Serum, Plasma, Tissue homogenate and Other biological samples

Assay Time

3.5H

Price($)

280 400

Size

48T 96T

Purchase details

Contact supplier to negotiate price details

100% Quality Assurance

Fast Shipping

Manual(EN) Manual(EN) MSDS MSDS
Product Details Performance Procedures Citations
Product Details
Product Name in English:
Mouse RAPGEF2(Rap Guanine Nucleotide Exchange Factor 2) ELISA Kit
Species:
Mouse
Alternative Name:
RAPGEF2, CNrasGEF, NRAPGEP, PDZ-GEF1, PDZGEF1, RA-GEF, RA-GEF-1, Rap-GEP, nRap GEP, Rap guanine nucleotide exchange factor 2
Uniport ID:
Q8CHG7
Assay Type:
Sandwich
Standard:
1000pg/mL
Sensitivity:
9.38 pg/mL
Detection Range:
15.63-1000pg/mL
Assay Time:
3.5H
Sample Type:
Serum, Plasma, Tissue homogenate and Other biological samples
Research:
Tumor immunity;Infection immunity;Developmental science;
Test Principle:
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to RAPGEF2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to RAPGEF2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain RAPGEF2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of RAPGEF2 in the samples is then determined by comparing the OD of the samples to the standard curve.
Technical Data
As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e.g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.
Concentration OD1 OD2 Average OD Corrected
1000 2.493 2.494 2.494 2.43
500 1.613 1.626 1.62 1.55
250 0.92 0.923 0.922 0.857
125 0.485 0.488 0.487 0.422
62.5 0.276 0.278 0.277 0.213
31.25 0.17 0.171 0.171 0.107
15.63 0.119 0.12 0.12 0.056
0 0.063 0.063 0.063 0
Linear
Samples were spiked with high concentrations of target proteins and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
Serum (n=5) EDTA plasma (n=5) Cell culture media (n=5)
1:2 Range (%) 85-94 90-99 80-92
Average (%) 92 95 87
1:4 Range (%) 90-99 95-106 86-102
Average (%) 92 101 89
1:8 Range (%) 95-102 87-101 87-103
Average (%) 100 96 98
1:16 Range (%) 82-90 82-97 85-101
Average (%) 88 94 90
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level were tested on 3 different plates, 20 replicates in each plate, respectively.
Item Intra-assay Precision Intra-assay Precision
Sample 3 3
Replicate 9 18
CV(%) 5 8
Rate of recovery
The recovery of spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
Sample Type Range(%) Average Recovery(%)
Serum (n=8) 87-99 93
EDTA plasma (n=8) 80-92 85
Cell culture media (n=8) 85-99 92
Assay Procedures
Related literature

Social Media