Human MMP-1 enzyme-linked immunoassay kit

CAT: EH0290 Datasheet
Specification 96 Test
Sensitivity 11.29 pg/ml (50 μl);14.24 pg/ml (10 μl);
Standard Curve Range 40.96~10000 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 Ready-to-Use
Operation Duration 120min
pg/ml O.D. Average Corrected
0.00 0.0274 0.0274 0.0274
40.96 0.0411 0.0406 0.0409 0.0135
102.40 0.0654 0.0681 0.0668 0.0394
256.00 0.1190 0.1274 0.1232 0.0958
640.00 0.2596 0.2716 0.2656 0.2382
1600.00 0.5838 0.5924 0.5881 0.5607
4000.00 1.3170 1.4010 1.3590 1.3316
10000.00 2.6860 2.8560 2.7710 2.7436

Precision

Intra-assay Precision Inter-assay Precision
Sample Number S1 S2 S3 S1 S2 S3
22 22 22 6 6 6
Average(pg/ml) 194.7 1006.1 2864.5 191.6 887.7 2620.7
Standard Deviation 13.2 60.8 221.1 13.5 65.3 80.9
Coefficient of Variation(%) 6.8 6.0 7.7 7.0 7.4 3.1

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 MMP-1 into health human serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 80% to 121% with an overall mean recovery of 114%.

Sample Values

Sample Matrix Sample Evaluated Range (pg/ml) Detectable (%) Mean of Detectable (pg/ml)
Serum30n.d.-42.8931.2518.13

Serum/Plasma– Thirty samples from apparently healthy volunteers serum were evaluated for the presence of human MMP-1 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: MMP-1

Matrix metalloproteinases are a family of zinc and calcium dependent endopeptidases with the combined ability to degrade all the components of the extracellular matrix. MMP-1 (interstitial collagenase), can degrade a broad range of substrates including types I, II, III, VII, VIII, and X collagens as well as casein, gelatin,
alpha ‑1 antitrypsin, myelin basic protein, L-Selectin, pro-TNF, IL-1 beta, IGF-BP3, IGF-BP5, pro MMP-2 and pro MMP-9. A significant role of MMP-1 is the degradation of fibrillar collagens in extracellular matrix remodeling, characterized by the cleavage of the interstitial collagen triple helix into ¾, ¼ fragments. However, as the list of substrates above illustrates, the role of MMP-1 is more diverse than originally envisaged, and may involve enzyme cascades, cytokine regulation and cell surface molecule modulation. MMP-1 is expressed by fibroblasts, keratinocytes, endothelial cells, monocytes and macrophages. Structurally, MMP-1 may be divided into several distinct domains; a pro-domain which is cleaved upon activation; a catalytic domain containing the zinc binding site; a short hinge region and a carboxyl terminal (hemopexin-like) domain.

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