Human TM(Thrombomodulin) ELISA Kit

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Human Thrombomodulin (TM) in Plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Human Thrombomodulin (TM) in samples from Plasma with no significant corss-reactivity with analogues from other species.

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

Description: A sandwich ELISA kit for quantitative measurement of Human TM (Thrombomodulin) in samples from Serum, Plasma, Cell supernatant

Description: A sandwich ELISA kit for detection of Thrombomodulin from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.

Description: A sandwich quantitative ELISA assay kit for detection of Rat Thrombomodulin (TM) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Rat Thrombomodulin (TM) in samples from plasma.

Description: Quantitativecompetitive ELISA kit for measuring Dog thrombomodulin, TM in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.

Description: Quantitativecompetitive ELISA kit for measuring Dog thrombomodulin, TM in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.

Description: Quantitativesandwich ELISA kit for measuring Pig thrombomodulin, TM in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.

Description: Quantitativesandwich ELISA kit for measuring Pig thrombomodulin, TM in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.

Description: Quantitativesandwich ELISA kit for measuring Rat thrombomodulin, TM in samples from serum, plasma, tissue homogenates, cell lysates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.

Description: Quantitativesandwich ELISA kit for measuring Rat thrombomodulin, TM in samples from serum, plasma, tissue homogenates, cell lysates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Dog Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Dog Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Dog Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Dog Thrombomodulin (TM) in Plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Dog Thrombomodulin (TM) in samples from Plasma. with no significant corss-reactivity with analogues from other species.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Pig Thrombomodulin (TM) in plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Pig Thrombomodulin (TM) in samples from plasma with no significant corss-reactivity with analogues from other species.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Thrombomodulin (TM) in Plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Thrombomodulin (TM) in Plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Rat Thrombomodulin (TM) in samples from Plasma with no significant corss-reactivity with analogues from other species.

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

Description: A sandwich quantitative ELISA assay kit for detection of Mouse Thrombomodulin (TM) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Mouse Thrombomodulin (TM) in samples from plasma.

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Mus ;Sensitivity: 37.5pg/ml

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombomodulin (TM) in plasma.

Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Mouse Thrombomodulin (TM) in plasma.

Description: Enzyme-linked immunosorbent assay based on the Double-antibody Sandwich method for detection of Mouse Thrombomodulin (TM) in samples from plasma with no significant corss-reactivity with analogues from other species.

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

Description: A sandwich quantitative ELISA assay kit for detection of Canine Thrombomodulin (TM) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Canine Thrombomodulin (TM) in samples from plasma.

Description: A sandwich quantitative ELISA assay kit for detection of Rabbit Thrombomodulin (TM) in samples from serum, plasma or other biological fluids.

Description: A sandwich quantitative ELISA assay kit for detection of Rabbit Thrombomodulin (TM) in samples from serum, plasma or other biological fluids.

Description: Method of detection: Double Antibody, Sandwich ELISA;Reacts with: Rabbit;Sensitivity: 37.5pg/ml