Mouse CCL2/MCP-1 enzyme-linked immunoassay kit

CAT: EM0025 Datasheet
Specification 96 Test
Sensitivity 1.78 pg/ml (10 μl)
Standard Curve Range 6.86~5000 pg/ml
Standard Curve Gradient 7 Points/3 Folds
Number of Incubations 2
Sample Volume 10 μl
Type Fully Ready-to-Use
Operation Duration 120min
pg/ml O.D. Average Corrected
0.00 0.0074 0.0068 0.0071
6.86 0.0115 0.0114 0.0115 0.0044
20.58 0.0150 0.0166 0.0158 0.0087
61.73 0.0318 0.0326 0.0322 0.0251
185.19 0.0893 0.0986 0.0940 0.0869
555.56 0.2921 0.3009 0.2965 0.2894
1666.67 1.1280 1.1620 1.1450 1.1379
5000.00 3.5970 3.5747 3.5859 3.5788

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(pg/ml) 122.5 532.2 1655.9 135.6 526.3 1598.4
Standard Deviation 9.1 23.5 68.1 8.4 24.1 60.7
Coefficient of Variation(%) 7.4 4.4 4.1 6.2 4.6 3.8

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 mouse CCL2 into health mouse serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 86% to 119% with an overall mean recovery of 108%.

Sample Values

Sample Matrix Sample Evaluated Range (pg/ml) Detectable (%) Mean of Detectable (pg/ml)
Serum 30 29.88-82.71 100 51.74

Serum/Plasma – Thirty samples from apparently healthy mice were evaluated for the presence of CCL2 in this assay. No medical histories were available for the donors. n.d. = non-detectable. Samples measured below the sensitivity are considered to be non-detectable.

Background: CCL2/MCP-1

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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