ELK9489-96T, Cattle LDH(Lactate Dehydrogenase) ELISA Kit, 96T

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ELK9490-96T, Chicken SEPP1(Selenoprotein P1, Plasma) ELISA Kit, 96T

ELK9490-96T, Chicken SEPP1(Selenoprotein P1, Plasma) ELISA Kit, 96T

ELK9490-48T, Chicken SEPP1(Selenoprotein P1, Plasma) ELISA Kit, 48T

2.142,00 RON

Chicken SEPP1(Selenoprotein P1, Plasma) ELISA Kit

SKU
ELK9490-48T

Alternative Names: SEPP; SeP; SEP-P1; SELP

Species: Chicken

Assay Type: Sandwich

Sensitivity: 29.6 pg/mL

Standard: 4000 pg/mL

Detection range: 62.5-4000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;Infection 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 Chicken SEPP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken SEPP1. 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 Chicken SEPP1, 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 Chicken SEPP1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: SEPP; SeP; SEP-P1; SELP

Species: Chicken

Assay Type: Sandwich

Sensitivity: 29.6 pg/mL

Standard: 4000 pg/mL

Detection range: 62.5-4000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Metabolic pathway;Infection 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 Chicken SEPP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken SEPP1. 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 Chicken SEPP1, 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 Chicken SEPP1 in the samples is then determined by comparing the OD of the samples to the standard curve.