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ELK7851-48T, LXA4(Lipoxin A4) ELISA Kit, 48T
1.814,75 RON
LXA4(Lipoxin A4) ELISA Kit
SKU
ELK7851-48T
Alternative Names: LX-A4
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 175.4 pg/mL
Standard: 40000 pg/mL
Detection range: 625-40000 pg/mL
Sample type: serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Assay length: 2h
Research Area: Signal transduction;Metabolic pathway;Infection immunity;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with LXA4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to LXA4. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of LXA4 in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 1.525,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: LX-A4 Species: General Assay Type: Competitive Inhibition Sensitivity: 175.4 pg/mL Standard: 40000 pg/mL Detection range: 625-40000 pg/mL Sample type: serum, plasma, tissue homogenates, cell culture supernates and other biological fluids Assay length: 2h Research Area: Signal transduction;Metabolic pathway;Infection immunity; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with LXA4 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to LXA4. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of LXA4 in the samples is then determined by comparing the OD of the samples to the standard curve. |
