ELK4257-48T, Goat HB(Hemoglobin) ELISA Kit, 48T

ELK4257-48T, Goat HB(Hemoglobin) ELISA Kit, 48T

ELK4258-48T, Pig HB(Hemoglobin) ELISA Kit, 48T

ELK4258-48T, Pig HB(Hemoglobin) ELISA Kit, 48T

ELK4257-96T, Goat HB(Hemoglobin) ELISA Kit, 96T

3.736,60 RON

Goat HB(Hemoglobin) ELISA Kit

SKU
ELK4257-96T

Alternative Names: Hgb; Haemoglobin; Heterotetramer(αβ)2

Species: Goat

Assay Type: Sandwich

Sensitivity: 2.7 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 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 Goat HB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Goat 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 Goat 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 Goat HB in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Hgb; Haemoglobin; Heterotetramer(αβ)2

Species: Goat

Assay Type: Sandwich

Sensitivity: 2.7 ng/mL

Standard: 500 ng/mL

Detection range: 7.82-500 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 Goat HB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Goat 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 Goat 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 Goat HB in the samples is then determined by comparing the OD of the samples to the standard curve.