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ELK8264-48T, PEG(Polyethylene Glycol) ELISA Kit, 48T
1.814,75 RON
PEG(Polyethylene Glycol) ELISA Kit
SKU
ELK8264-48T
Alternative Names: PEO; POE; Polyethylene oxide; Polyoxyethylene; Carbowax; GoLYTELY; GlycoLax; Fortrans; TriLyte; Colyte; Halflytely; Macrogol; MiraLAX; MoviPrep
Species: General
Assay Type: Competitive Inhibition
Sensitivity: 4.72 ng/mL
Standard: 1000 ng/mL
Detection range: 15.63-1000 ng/mL
Sample type: biological agents
Assay length: 2h
Research Area: Gastrointestinal science
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PEG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PEG. 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 PEG 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: PEO; POE; Polyethylene oxide; Polyoxyethylene; Carbowax; GoLYTELY; GlycoLax; Fortrans; TriLyte; Colyte; Halflytely; Macrogol; MiraLAX; MoviPrep Species: General Assay Type: Competitive Inhibition Sensitivity: 4.72 ng/mL Standard: 1000 ng/mL Detection range: 15.63-1000 ng/mL Sample type: biological agents Assay length: 2h Research Area: Gastrointestinal science Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PEG protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PEG. 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 PEG in the samples is then determined by comparing the OD of the samples to the standard curve. |
