24T ELISA Kit Trial Size (Only USD$150/ kit)
* The sample kit cost can be deducted from your subsequent orders of 96T full size kits of the same analyte at 1/5 per kit, until depleted in 6 months. Apply now
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|Intra-assay Precision (Precision within an assay): CV%<8%|
|Three samples of known concentration were tested twenty times on one plate to assess.|
|Inter-assay Precision (Precision between assays): CV%<10%|
|Three samples of known concentration were tested in twenty assays to assess.|
|To assess the linearity of the assay, samples were spiked with high concentrations of human ITG/CD11b in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.|
|The recovery of human ITG/CD11b spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.|
|Sample Type||Average % Recovery||Range|
|EDTA plasma (n=4)||96||92-102|
|These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.|
This human ITGAM ELISA kit employs the quantitative sandwich enzyme immunoassay technique to measure the levels of human ITGAM in multiple samples, including serum, plasma, or tissue homogenates. It also uses the enzyme-substrate chromogenic reaction to visualize and analyze the analyte levels through the color intensity. The intensity of the colored product is in direct proportion to the ITGAM levels in the sample and is measured at 450 nm through a microplate reader.
ITGAM is the encoding gene for CD11b, highly expressed on the surface of innate immune cells, including macrophages and neutrophils, which together with CD18, form Mac-1 or CR3, a protein that mediates leukocyte adhesion, migration, and phagocytosis in different cells including neutrophils, monocytes, macrophages, and dendritic cells. CD11b also contributes to the phagocytosis of opsonized particles, including apoptotic cells and the immune complex. It has consistently been associated with susceptibility to systemic lupus erythematosus (SLE).
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