ELK7859-96T, Human Anti-Apo(Anti-Apolipoprotein Antibody) ELISA Kit, 96T

ELK7859-96T, Human Anti-Apo(Anti-Apolipoprotein Antibody) ELISA Kit, 96T

ELK7860-96T, TXB2(Thromboxane B2) ELISA Kit, 96T

ELK7860-96T, TXB2(Thromboxane B2) ELISA Kit, 96T

ELK7860-48T, TXB2(Thromboxane B2) ELISA Kit, 48T

1.814,75 RON

TXB2(Thromboxane B2) ELISA Kit

SKU
ELK7860-48T

Alternative Names: TX-B2

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 7.2 pg/mL

Standard: 1500 pg/mL

Detection range: 23.44-1500 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TXB2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TXB2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 TXB2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: TX-B2

Species: General

Assay Type: Competitive Inhibition

Sensitivity: 7.2 pg/mL

Standard: 1500 pg/mL

Detection range: 23.44-1500 pg/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 2h

Research Area: Metabolic pathway;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with TXB2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TXB2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 TXB2 in the samples is then determined by comparing the OD of the samples to the standard curve.