ELK3771-96T, Human NKRF(NFKB Repressing Factor) ELISA Kit, 96T

ELK3771-96T, Human NKRF(NFKB Repressing Factor) ELISA Kit, 96T

ELK3772-96T, Human CREBBP(CREB Binding Protein) ELISA Kit, 96T

ELK3772-96T, Human CREBBP(CREB Binding Protein) ELISA Kit, 96T

ELK3772-48T, Human CREBBP(CREB Binding Protein) ELISA Kit, 48T

2.142,00 RON

Human CREBBP(CREB Binding Protein) ELISA Kit

SKU
ELK3772-48T

Alternative Names: CBP; RSTS; RTS; KAT3A; Rubinstein-Taybi Syndrome

Species: Human

Assay Type: Sandwich

Sensitivity: 0.132 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Neuro science;

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

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Description

Alternative Names: CBP; RSTS; RTS; KAT3A; Rubinstein-Taybi Syndrome

Species: Human

Assay Type: Sandwich

Sensitivity: 0.132 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: Tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Neuro science;

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