ELK1192-48T, Human uPA(Plasminogen Activator, Urokinase) ELISA Kit, 48T

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ELK1192-96T, Human uPA(Plasminogen Activator, Urokinase) ELISA Kit, 96T

2.475,20 RON

Human uPA(Plasminogen Activator, Urokinase) ELISA Kit

SKU
ELK1192-96T

Alternative Names: PLAU; ATF; URK; UK; UP-A; Abbokinase; Urokinase-Type Plasminogen Activator

Species: Human

Assay Type: Sandwich

Sensitivity: 6.8 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

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

Assay length: 3.5h

Research Area: Tumor immunity;

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 uPA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human uPA. 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 uPA, 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 uPA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PLAU; ATF; URK; UK; UP-A; Abbokinase; Urokinase-Type Plasminogen Activator

Species: Human

Assay Type: Sandwich

Sensitivity: 6.8 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

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

Assay length: 3.5h

Research Area: Tumor immunity;

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 uPA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human uPA. 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 uPA, 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 uPA in the samples is then determined by comparing the OD of the samples to the standard curve.