ELK4082-48T, Human CCNB(Cyclin B) ELISA Kit, 48T

ELK4082-48T, Human CCNB(Cyclin B) ELISA Kit, 48T

ELK4083-48T, Human CCNB2(Cyclin B2) ELISA Kit, 48T

ELK4083-48T, Human CCNB2(Cyclin B2) ELISA Kit, 48T

ELK4082-96T, Human CCNB(Cyclin B) ELISA Kit, 96T

2.963,10 RON

Human CCNB(Cyclin B) ELISA Kit

SKU
ELK4082-96T

Alternative Names: CCNB1; CCN-B; G2/Mitotic-Specific Cyclin B1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.117 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: tissue homogenates, cell lysates 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 CCNB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CCNB. 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 CCNB, 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 CCNB in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: CCNB1; CCN-B; G2/Mitotic-Specific Cyclin B1

Species: Human

Assay Type: Sandwich

Sensitivity: 0.117 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: tissue homogenates, cell lysates 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 CCNB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CCNB. 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 CCNB, 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 CCNB in the samples is then determined by comparing the OD of the samples to the standard curve.