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ELK1352-48T, Horse HB(Hemoglobin) ELISA Kit, 48T
2.439,50 RON
Horse HB(Hemoglobin) ELISA Kit
SKU
ELK1352-48T
Alternative Names: Hgb; Haemoglobin; Heterotetramer(αβ)2
Species: Horse
Assay Type: Sandwich
Sensitivity: 3.7 ng/mL
Standard: 600 ng/mL
Detection range: 9.38-600 ng/mL
Sample type: Serum, plasma, erythrocyte lysates.
Assay length: 3.5h
Research Area: Metabolic pathway;Infection immunity;Hematology;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 Horse HB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse HB. 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 HB, 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 HB in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 2.050,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: Hgb; Haemoglobin; Heterotetramer(αβ)2 Species: Horse Assay Type: Sandwich Sensitivity: 3.7 ng/mL Standard: 600 ng/mL Detection range: 9.38-600 ng/mL Sample type: Serum, plasma, erythrocyte lysates. Assay length: 3.5h Research Area: Metabolic pathway;Infection immunity;Hematology;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 Horse HB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse HB. 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 HB, 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 HB in the samples is then determined by comparing the OD of the samples to the standard curve. |
