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Catalog Number:RE2420H
Human MRC2(Mannose Receptor C Type 2) ELISA Kit

Size:

48 T

96 T

Price:

$279.00

$399.00

Delivery: Order now, ship in 3 days

Product Details
Product Name Human MRC2(Mannose Receptor C Type 2) ELISA Kit Species Human
Uniprot ID Q9UBG0 Alternative Names CD28,C-type lectin domain family 13 member E,Endocytic receptor 18,Macrophage mannose receptor 2,Urokinase-type plasminogen activator receptor-associated protein,UPAR-associated protein,Urokinase receptor-associated protein
Detection method Sandwich Sensitivity 0.19 ng/mL
Standard 20ng/mL Detection Range 0.32-20ng/mL
Sample type Serum, Plasma, Tissue homogenate and Other biological samples;Sample Volume=100μL
Reaction time 3.5H Research Area Metabolic pathway;Endocrinology;Cardiovascular biology;Developmental science;Bone metabolism;
Test principle 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 Human MRC2. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human MRC2 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 Human MRC2, 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 Human MRC2. You can calculate the concentration of Human MRC2 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.

(ng/mL) OD Corrected
20.00 2.336 2.284
10.00 1.542 1.490
5.00 0.911 0.859
2.50 0.428 0.376
1.25 0.249 0.197
0.63 0.149 0.097
0.32 0.102 0.050
0.00 0.052 0.000
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.

Intra-assay Precision Inter-assay Precision
Sample 1 2 3 1 2 3
n 20 20 20 20 20 20
Mean(ng/mL) 0.35 4.04 9.02 0.65 4.19 6.31
Standard deviation 0.02 0.23 0.33 0.02 0.15 0.38
C V (%) 4.41 4.29 6.95 3.31 4.55 7.36
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) 86-99 92
EDTA plasma (n=8) 80-95 87
Cell culture media (n=8) 83-95 89
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 (%) 92-103 95-101 89-98
Average (%) 95 99 96
1:4 Range (%) 82-96 98-102 95-103
Average (%) 93 100 101
1:8 Range (%) 80-91 86-92 99-106
Average (%) 91 86 102
1:16 Range (%) 97-103 81-93 80-92
Average (%) 100 81 91
Assay Procedures