ELK8253-96T, Mouse IFNa11(Interferon Alpha 11) ELISA Kit, 96T

ELK8253-96T, Mouse IFNa11(Interferon Alpha 11) ELISA Kit, 96T

ELK8254-96T, PCr(Phosphocreatine) ELISA Kit, 96T

ELK8254-96T, PCr(Phosphocreatine) ELISA Kit, 96T

ELK8254-48T, PCr(Phosphocreatine) ELISA Kit, 48T

1.814,75 RON

PCr(Phosphocreatine) ELISA Kit

SKU
ELK8254-48T

Alternative Names: CP; Creatine Phosphate; Phosphorylcreatine; Creatine-P; Phosphagen; Fosfocreatine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 49.3 ng/mL

Standard: 10000 ng/mL

Detection range: 156.25-10000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PCr protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PCr. 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 PCr in the samples is then determined by comparing the OD of the samples to the standard curve.

Mai multe informatii
Price 1.525,00 RON (preturile sunt fara TVA)
Description

Alternative Names: CP; Creatine Phosphate; Phosphorylcreatine; Creatine-P; Phosphagen; Fosfocreatine

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 49.3 ng/mL

Standard: 10000 ng/mL

Detection range: 156.25-10000 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PCr protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PCr. 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 PCr in the samples is then determined by comparing the OD of the samples to the standard curve.