Human MCP-3/CCL7 enzyme-linked immunoassay kit

CAT: EH0269 Datasheet
Specification 96 Test
Sensitivity 10.11 pg/ml (50 μl);46.63 pg/ml (10 μl);
Standard Curve Range 31.25 ~2000 pg/ml
Standard Curve Gradient 7 Points
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 0.0089 0.0089 0.0089
31.25 0.0127 0.0124 0.0126 0.0037
62.50 0.0223 0.0206 0.0215 0.0126
125.00 0.0541 0.0563 0.0552 0.0463
250.00 0.1972 0.1833 0.1903 0.1814
500.00 0.6470 0.6402 0.6436 0.6347
1000.00 1.9170 1.8810 1.8990 1.8901
2000.00 4.2123 4.0995 4.1559 4.1470

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(pg/ml) 35.2 192.7 582.6 32.6 199.9 586.6
Standard Deviation 2.5 6.2 22.7 2.5 5.2 20.2
Coefficient of Variation(%) 7.2 3.2 3.9 7.6 2.6 3.5

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty-two 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 MCP-3/CCL7 into health human serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 80% to 115% with an overall mean recovery of 98%.

Sample Values

Sample Matrix Sample Evaluated Range (pg/ml) Detectable (%) Mean of Detectable (pg/ml)
Serum30n.d.-1134.3194565.01

Serum/Plasma – Thirty samples from apparently healthy volunteers were evaluated for the presence of human MCP-3/CCL7 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: MCP-3/CCL7

Mouse MARC, a member of the beta subfamily of chemokines, was initially identified as a transcript that is induced in a mouse mast cell line after Fc epsilon RI triggering by IgE plus antigen. Sequence comparisons suggest that MARC may be the mouse homologue of the human MCP-3 gene. Mouse MARC/MCP-3 expression has also been detected during murine experimental allergic encephalomyelitis in the spinal cord, and in LPS-stimulated murine WEHI -3 cells and Swiss 3T3 cells where MARC expression is glucocorticoid-attenuated. Except for one amino acid subsititution, mouse MARC is identical to mouse FIC, the product of a growth factor‑activated gene. The mouse MARC cDNA encodes a 97 amino acid residue precursor protein with a 23 amino acid residue signal peptide that is cleaved to yield a 74 amino acid residue mature protein. Mouse CCR2, a mouse chemokine receptor, has been shown to bind JE/MCP-1 with high affinity and MARC/MCP-3 with lower affinity.

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