ELK0908-96T, Human SETDB1(Histone-lysine N-methyltransferase SETDB1) ELISA Kit, 96T

ELK0908-96T, Human SETDB1(Histone-lysine N-methyltransferase SETDB1) ELISA Kit, 96T

ELK0909-96T, Human CTN(Creatinine) ELISA Kit, 96T

ELK0909-96T, Human CTN(Creatinine) ELISA Kit, 96T

ELK0909-48T, Human CTN(Creatinine) ELISA Kit, 48T

1.814,75 RON

Human CTN(Creatinine) ELISA Kit

SKU
ELK0909-48T

Alternative Names: Creatinine

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 1.41 µg/mL

Standard: 200 µg/mL

Detection range: 3.13-200 µg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Metabolism

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

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Description

Alternative Names: Creatinine

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 1.41 µg/mL

Standard: 200 µg/mL

Detection range: 3.13-200 µg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Metabolism

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