Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in samples from serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids with no significant corss-reactivity with analogues from other species. This is a cost efficient bulk pack of 10 plates of 96 wells each, conveniently packed along with the other reagents in 10 separate kits to avoid unsealing the plates and reagents that won't be immediately used.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.

Description: A sandwich ELISA kit for detection of Epithelial Neutrophil Activating Peptide 78 from Mouse in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: 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 ENA78. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ENA78. 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 ENA78, 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 ENA78 in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: 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 ENA78. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat ENA78. 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 ENA78, 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 ENA78 in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma and other biological fluids.

Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma and other biological fluids.

Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma and other biological fluids.

Description: This is Double-antibody Sandwich Chemiluminescent immunoassay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78) in serum, plasma and other biological fluids.

Description: Double-antibody Sandwich chemiluminescent immunoassay for detection of Mouse Epithelial Neutrophil Activating Peptide 78 (ENA78)Serum, plasma and other biological fluids

Description: 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 Human ENA78. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ENA78. 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 Human ENA78, 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 Human ENA78 in the samples is then determined by comparing the OD of the samples to the standard curve.

Description: 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 Human ENA78. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ENA78. 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 Human ENA78, 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 Human ENA78 in the samples is then determined by comparing the OD of the samples to the standard curve.