Human CCL2/MCP-1 enzyme-linked immunoassay kit

CAT: EH0010 Datasheet
Specification 96 Test
Sensitivity 0.002 pg/ml (50 μl);0.02 pg/ml (10 μl)
Standard Curve Range 0.14~100 pg/ml
Standard Curve Gradient 7 Points/3 Folds
Number of Incubations 2
Detectable sample Liquid phase sample of soluble substances. For example: serum, plasma, cell culture supernatant, tissue grinding liquid, etc.
Sample Volume 50 μl/10 μl
Type Fully Ready-to-Use
Operation Duration 120min
pg/ml O.D. Average Corrected
0.00 0.0098 0.0091 0.0095
0.14 0.0280 0.0270 0.0275 0.0181
0.41 0.0654 0.0621 0.0638 0.0543
1.23 0.1784 0.1717 0.1751 0.1656
3.70 0.4950 0.4552 0.4751 0.4657
11.11 1.2670 1.1900 1.2285 1.2191
33.33 2.4260 2.3230 2.3745 2.3651
100.00 3.1270 3.0720 3.0995 3.0901

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(pg/ml) 1.1 5.2 15.4 0.9 5.1 15.2
Standard Deviation 0.1 0.3 0.9 8.4 24.1 60.7
Coefficient of Variation(%) 6.1 5.4 5.8 6.3 4.8 5.4

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays) Three samples of known concentration were tested six times on one plate to assess intra-assay precision.

Spike Recovery

The spike recovery was evaluated by spiking 3 levels of human CCL2/MCP-1 into health human serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 90% to 118% with an overall mean recovery of 103%.

Sample Values

Sample Matrix Sample Evaluated Range (pg/ml) Detectable (%) Mean of Detectable (pg/ml)
Serum 30 65.77-880.07 100 371.62

Serum/Plasma – Thirty samples from apparently healthy volunteers were evaluated for the presence of CCL2 in this assay. No medical histories were available for the donors.

Background: CCL2

CCL2/JE/MCP-1, is a chemokine that binds the receptor CCR2 and induces the chemoattraction of mononuclear cells. It induces the activation of monocytes, NK cells, lymphocytes, and basophils. Additionally, CCL2 promotes Th2 polarization in CD4+ T cells, and CCL2-mediated recruitment of monocytes to sites of inflammation contributes to disease severity in atherosclerosis, multiple sclerosis, and allergic asthma. Endogenous proteolytic trimming of CCL2 at the N-terminus, including the N-terminal pyrrolidone carboxylic acid-modified glutamine, downregulates activity but not receptor binding.

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