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ICAM-1/CD54 test kit RE2831R
for researchserumplasma

ICAM-1/CD54 test kit - RE2831R - ReedBiotech - for research / serum / plasma
ICAM-1/CD54 test kit - RE2831R - ReedBiotech - for research / serum / plasma
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Characteristics

Applications
for research
Tested parameter
ICAM-1/CD54
Sample type
serum, plasma, tissue
Analysis mode
ELISA
Result display time

210 min

Sample volume

0.1 ml
(0.00338 US fl oz)

Description

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat ICAM-1/CD54. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat ICAM-1/CD54 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Rat ICAM-1/CD54, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat ICAM-1/CD54. You can calculate the concentration of Rat ICAM-1/CD54 in the samples 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. 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. Rate of recovery The recovery of spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices
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