ELK3896-48T, Human CRY1(Cryptochrome 1) ELISA Kit, 48T

ELK3896-48T, Human CRY1(Cryptochrome 1) ELISA Kit, 48T

ELK3897-48T, Human PAX9(Paired Box Gene 9) ELISA Kit, 48T

ELK3897-48T, Human PAX9(Paired Box Gene 9) ELISA Kit, 48T

ELK3896-96T, Human CRY1(Cryptochrome 1) ELISA Kit, 96T

2.963,10 RON

Human CRY1(Cryptochrome 1) ELISA Kit

SKU
ELK3896-96T

Alternative Names: PHLL1; Photolyase-like 1

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: Neuro science;Nutrition 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 CRY1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CRY1. 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 CRY1, 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 CRY1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: PHLL1; Photolyase-like 1

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: Neuro science;Nutrition 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 CRY1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human CRY1. 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 CRY1, 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 CRY1 in the samples is then determined by comparing the OD of the samples to the standard curve.