ELK4752-48T, Human ACTa2(Actin Alpha 2, Smooth Muscle) ELISA Kit, 48T

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ELK4752-96T, Human ACTa2(Actin Alpha 2, Smooth Muscle) ELISA Kit, 96T

2.475,20 RON

Human ACTa2(Actin Alpha 2, Smooth Muscle) ELISA Kit

SKU
ELK4752-96T

Alternative Names: α-SMA,ACT-A2; ACTSA; ACTVS; Asma; GIG46; Cell growth-inhibiting gene 46 protein; Smooth Muscle Actin

Species: Human

Assay Type: Sandwich

Sensitivity: 2.9 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 ng/mL

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

Assay length: 3.5h

Research Area: Developmental science;Bone metabolism;

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 ACTa2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACTa2. 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 ACTa2, 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 ACTa2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: α-SMA,ACT-A2; ACTSA; ACTVS; Asma; GIG46; Cell growth-inhibiting gene 46 protein; Smooth Muscle Actin

Species: Human

Assay Type: Sandwich

Sensitivity: 2.9 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 ng/mL

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

Assay length: 3.5h

Research Area: Developmental science;Bone metabolism;

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 ACTa2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ACTa2. 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 ACTa2, 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 ACTa2 in the samples is then determined by comparing the OD of the samples to the standard curve.