ELK8964-96T, Human SNCb(Synuclein beta) ELISA Kit, 96T

ELK8964-96T, Human SNCb(Synuclein beta) ELISA Kit, 96T

ELK8965-96T, Horse FG(Fibrinogen) ELISA Kit, 96T

ELK8965-96T, Horse FG(Fibrinogen) ELISA Kit, 96T

ELK8965-48T, Horse FG(Fibrinogen) ELISA Kit, 48T

2.142,00 RON

Horse FG(Fibrinogen) ELISA Kit

SKU
ELK8965-48T

Alternative Names: F1; FI; Fbg; Coagulation Factor I

Species: Horse

Assay Type: Sandwich

Sensitivity: 5.6 ng/mL

Standard: 800 ng/mL

Detection range: 12.5-800 ng/mL

Sample type: Plasma

Assay length: 3.5h

Research Area: Cardiovascular

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

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Description

Alternative Names: F1; FI; Fbg; Coagulation Factor I

Species: Horse

Assay Type: Sandwich

Sensitivity: 5.6 ng/mL

Standard: 800 ng/mL

Detection range: 12.5-800 ng/mL

Sample type: Plasma

Assay length: 3.5h

Research Area: Cardiovascular

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