ELK6464-96T, Mouse LTA4H(Leukotriene A4 Hydrolase) ELISA Kit, 96T

ELK6464-96T, Mouse LTA4H(Leukotriene A4 Hydrolase) ELISA Kit, 96T

ELK6465-96T, Rat F11(Coagulation Factor XI) ELISA Kit, 96T

ELK6465-96T, Rat F11(Coagulation Factor XI) ELISA Kit, 96T

ELK6465-48T, Rat F11(Coagulation Factor XI) ELISA Kit, 48T

2.142,00 RON

Rat F11(Coagulation Factor XI) ELISA Kit

SKU
ELK6465-48T

Alternative Names: FXI; PTA; Fletcher Factor; Prekallikrein; Plasma Thromboplastin Antecedent

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.21 ng/mL

Standard: 30 ng/mL

Detection range: 0.47-30 ng/mL

Sample type: plasma

Assay length: 3.5h

Research Area: Hematology;

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 Rat F11. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat F11. 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 Rat F11, 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 Rat F11 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: FXI; PTA; Fletcher Factor; Prekallikrein; Plasma Thromboplastin Antecedent

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.21 ng/mL

Standard: 30 ng/mL

Detection range: 0.47-30 ng/mL

Sample type: plasma

Assay length: 3.5h

Research Area: Hematology;

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 Rat F11. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat F11. 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 Rat F11, 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 Rat F11 in the samples is then determined by comparing the OD of the samples to the standard curve.