ELK9235-48T, Human TRY(Trypsin) ELISA Kit, 48T

ELK9235-48T, Human TRY(Trypsin) ELISA Kit, 48T

ELK9236-48T, Human AST2(Aspartate Aminotransferase 2) ELISA Kit, 48T

ELK9236-48T, Human AST2(Aspartate Aminotransferase 2) ELISA Kit, 48T

ELK9235-96T, Human TRY(Trypsin) ELISA Kit, 96T

3.736,60 RON

Human TRY(Trypsin) ELISA Kit

SKU
ELK9235-96T

Alternative Names: Trypsin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.066 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Human gene deletion;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human TRY. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TRY. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human TRY, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 TRY in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Trypsin

Species: Human

Assay Type: Sandwich

Sensitivity: 0.066 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 3.5h

Research Area: Human gene deletion;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human TRY. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TRY. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human TRY, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 TRY in the samples is then determined by comparing the OD of the samples to the standard curve.