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Linscott's Directory of Immunological & Biological Reagents
CLOUD-CLONE CORP.
 (http://www.cloud-clone.us)

CLOUD-CLONE CORP.

11271 Richmond Ave., Suite H104

Houston TX 77082

Phone: 1-832-538-0970

Phone: 1-888-960-7402

Fax: 1-832-538-0088

service@cloud-clone.us
Sales: sales@cloud-clone.us

Website: http://www.cloud-clone.us

 
CLOUD-CLONE CORP. Products - Page 2 of 200
Page 2 of 200
Records 26 - 50 of 4,999
Name Description Size Catalog #
8-Hydroxydeoxyguanosine (8-OHdG) ELISA Kit This assay has high sensitivity and excellent specificity for detection of 8-Hydroxydeoxyguanosine (8-OHdG) No significant cross-reactivity or interference between 8-Hydroxydeoxyguanosine (8-OHdG) and analogues was observed.. This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific for 8-Hydroxydeoxyguanosine (8-OHdG) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between Horseradish Peroxidase (HRP) labeled 8-Hydroxydeoxyguanosine (8-OHdG) and unlabeled 8-Hydroxydeoxyguanosine (8-OHdG) (Standards or samples) with the pre-coated antibody specific for 8-Hydroxydeoxyguanosine (8-OHdG). After incubation the unbound conjugate is washed off. The amount of bound HRP conjugate is reverse proportional to the concentration of 8-Hydroxydeoxyguanosine (8-OHdG) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of 8-Hydroxydeoxyguanosine (8-OHdG) in the sample.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 49.38-4000pg/mL The standard curve concentrations used for the ELISA's were 4000pg/mL, 1333.33pg/mL, 444.44pg/mL, 148.15pg/mL, 49.38pg/mL. The minimum detectable dose of this kit is typically less than 18.5pg/mL 96-well strip plate CEA660Ge
A Disintegrin And Metalloprotease 10 (ADAM10) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 10 (ADAM10) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 10 (ADAM10) and analogues was observed.. 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 A Disintegrin And Metalloprotease 10 (ADAM10). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 10 (ADAM10). 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 A Disintegrin And Metalloprotease 10 (ADAM10), 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 A Disintegrin And Metalloprotease 10 (ADAM10) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 62.5-4000pg/mL The standard curve concentrations used for the ELISA's were 4000pg/mL, 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL. The minimum detectable dose of this kit is typically less than 24.6pg/mL 96-well strip plate SEA766Hu
A Disintegrin And Metalloprotease 10 (ADAM10) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Rat A Disintegrin And Metalloprotease 10 (ADAM10) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 10 (ADAM10) and analogues was observed.. 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 A Disintegrin And Metalloprotease 10 (ADAM10). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 10 (ADAM10). 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 A Disintegrin And Metalloprotease 10 (ADAM10), 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 A Disintegrin And Metalloprotease 10 (ADAM10) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 78.125-5000pg/mL The standard curve concentrations used for the ELISA's were 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312.5pg/mL, 156.25pg/mL, 78.125pg/mL. The minimum detectable dose of this kit is typically less than 27pg/mL 96-well strip plate SEA766Ra
A Disintegrin And Metalloprotease 12 (ADAM12) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 12 (ADAM12) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 12 (ADAM12) and analogues was observed.. 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 A Disintegrin And Metalloprotease 12 (ADAM12). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 12 (ADAM12). 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 A Disintegrin And Metalloprotease 12 (ADAM12), 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 A Disintegrin And Metalloprotease 12 (ADAM12) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 78.125-5000pg/mL The standard curve concentrations used for the ELISA's were 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312.5pg/mL, 156.25pg/mL, 78.125pg/mL. The minimum detectable dose of this kit is typically less than 28pg/mL 96-well strip plate SEK242Hu
A Disintegrin And Metalloprotease 15 (ADAM15) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 15 (ADAM15) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 15 (ADAM15) and analogues was observed.. 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 A Disintegrin And Metalloprotease 15 (ADAM15). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 15 (ADAM15). 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 A Disintegrin And Metalloprotease 15 (ADAM15), 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 A Disintegrin And Metalloprotease 15 (ADAM15) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.054ng/mL 96-well strip plate SEJ800Hu
A Disintegrin And Metalloprotease 17 (ADAM17) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 17 (ADAM17) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 17 (ADAM17) and analogues was observed.. 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 A Disintegrin And Metalloprotease 17 (ADAM17). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 17 (ADAM17). 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 A Disintegrin And Metalloprotease 17 (ADAM17), 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 A Disintegrin And Metalloprotease 17 (ADAM17) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.063ng/mL 96-well strip plate SEB555Hu
A Disintegrin And Metalloprotease 17 (ADAM17) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Rat A Disintegrin And Metalloprotease 17 (ADAM17) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 17 (ADAM17) and analogues was observed.. 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 A Disintegrin And Metalloprotease 17 (ADAM17). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 17 (ADAM17). 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 A Disintegrin And Metalloprotease 17 (ADAM17), 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 A Disintegrin And Metalloprotease 17 (ADAM17) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.313-20ng/mL The standard curve concentrations used for the ELISA's were 20ng/mL, 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL. The minimum detectable dose of this kit is typically less than 0.112ng/mL 96-well strip plate SEB555Ra
A Disintegrin And Metalloprotease 19 (ADAM19) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 19 (ADAM19) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 19 (ADAM19) and analogues was observed.. 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 A Disintegrin And Metalloprotease 19 (ADAM19). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 19 (ADAM19). 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 A Disintegrin And Metalloprotease 19 (ADAM19), 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 A Disintegrin And Metalloprotease 19 (ADAM19) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates and other biological fluids.. Detection Range: 0.313-20ng/mL The standard curve concentrations used for the ELISA's were 20ng/mL, 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL. The minimum detectable dose of this kit is typically less than 0.108ng/mL 96-well strip plate SEK240Hu
A Disintegrin And Metalloprotease 22 (ADAM22) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 22 (ADAM22) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 22 (ADAM22) and analogues was observed.. 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 A Disintegrin And Metalloprotease 22 (ADAM22). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 22 (ADAM22). 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 A Disintegrin And Metalloprotease 22 (ADAM22), 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 A Disintegrin And Metalloprotease 22 (ADAM22) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.057ng/mL 96-well strip plate SEK165Hu
A Disintegrin And Metalloprotease 28 (ADAM28) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 28 (ADAM28) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 28 (ADAM28) and analogues was observed.. 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 A Disintegrin And Metalloprotease 28 (ADAM28). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 28 (ADAM28). 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 A Disintegrin And Metalloprotease 28 (ADAM28), 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 A Disintegrin And Metalloprotease 28 (ADAM28) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.061ng/mL 96-well strip plate SEK202Hu
A Disintegrin And Metalloprotease 33 (ADAM33) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 33 (ADAM33) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 33 (ADAM33) and analogues was observed.. 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 A Disintegrin And Metalloprotease 33 (ADAM33). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 33 (ADAM33). 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 A Disintegrin And Metalloprotease 33 (ADAM33), 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 A Disintegrin And Metalloprotease 33 (ADAM33) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.060ng/mL 96-well strip plate SEP196Hu
A Disintegrin And Metalloprotease 8 (ADAM8) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 8 (ADAM8) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 8 (ADAM8) and analogues was observed.. 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 A Disintegrin And Metalloprotease 8 (ADAM8). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 8 (ADAM8). 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 A Disintegrin And Metalloprotease 8 (ADAM8), 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 A Disintegrin And Metalloprotease 8 (ADAM8) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates, cell lysates and other biological fluids.. Detection Range: 6.25-400pg/mL The standard curve concentrations used for the ELISA's were 400pg/mL, 200pg/mL, 100pg/mL, 50pg/mL, 25pg/mL, 12.5pg/mL, 6.25pg/mL. The minimum detectable dose of this kit is typically less than 2.35pg/mL 96-well strip plate SEA620Hu
A Disintegrin And Metalloprotease 8 (ADAM8) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Mouse A Disintegrin And Metalloprotease 8 (ADAM8) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 8 (ADAM8) and analogues was observed.. 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 A Disintegrin And Metalloprotease 8 (ADAM8). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 8 (ADAM8). 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 A Disintegrin And Metalloprotease 8 (ADAM8), 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 A Disintegrin And Metalloprotease 8 (ADAM8) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 15.625-1000pg/mL The standard curve concentrations used for the ELISA's were 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.25pg/mL, 15.625pg/mL. The minimum detectable dose of this kit is typically less than 5.7pg/mL 96-well strip plate SEA620Mu
A Disintegrin And Metalloprotease 9 (ADAM9) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloprotease 9 (ADAM9) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 9 (ADAM9) and analogues was observed.. 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 A Disintegrin And Metalloprotease 9 (ADAM9). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 9 (ADAM9). 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 A Disintegrin And Metalloprotease 9 (ADAM9), 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 A Disintegrin And Metalloprotease 9 (ADAM9) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates ,cell culture supernates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.064ng/mL 96-well strip plate SEB829Hu
A Disintegrin And Metalloprotease 9 (ADAM9) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Rat A Disintegrin And Metalloprotease 9 (ADAM9) No significant cross-reactivity or interference between A Disintegrin And Metalloprotease 9 (ADAM9) and analogues was observed.. 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 A Disintegrin And Metalloprotease 9 (ADAM9). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloprotease 9 (ADAM9). 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 A Disintegrin And Metalloprotease 9 (ADAM9), 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 A Disintegrin And Metalloprotease 9 (ADAM9) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.054ng/mL 96-well strip plate SEB829Ra
A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1). 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1), 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 1.563-100ng/mL The standard curve concentrations used for the ELISA's were 100ng/mL, 50ng/mL, 25ng/mL, 12.5ng/mL, 6.25ng/mL, 3.125ng/mL, 1.563ng/mL. The minimum detectable dose of this kit is typically less than 0.54ng/mL 96-well strip plate SEB973Hu
A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Rat A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1). 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1), 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 A Disintegrin And Metalloproteinase With Thrombospondin 1 (ADAMTS1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 78.125-5000pg/mL The standard curve concentrations used for the ELISA's were 5000pg/mL, 2500pg/mL, 1250pg/mL, 625pg/mL, 312.5pg/mL, 156.25pg/mL, 78.125pg/mL. The minimum detectable dose of this kit is typically less than 30.5pg/mL 96-well strip plate SEB973Ra
A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4). 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 A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4), 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 A Disintegrin And Metalloproteinase With Thrombospondin 4 (ADAMTS4) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates and other biological fluids.. Detection Range: 62.5-4000pg/mL The standard curve concentrations used for the ELISA's were 4000pg/mL, 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL. The minimum detectable dose of this kit is typically less than 26.3pg/mL 96-well strip plate SEK204Hu
A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5). 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 A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5), 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 A Disintegrin And Metalloproteinase With Thrombospondin 5 (ADAMTS5) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 0.313-20ng/mL The standard curve concentrations used for the ELISA's were 20ng/mL, 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL. The minimum detectable dose of this kit is typically less than 0.112ng/mL 96-well strip plate SEK205Hu
A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7). 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7), 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.059ng/mL 96-well strip plate SEB974Hu
A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Rat A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7). 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7), 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 A Disintegrin And Metalloproteinase With Thrombospondin 7 (ADAMTS7) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.058ng/mL 96-well strip plate SEB974Ra
A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9) No significant cross-reactivity or interference between A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9) and analogues was observed.. 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 A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9). 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 A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9), 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 A Disintegrin And Metalloproteinase With Thrombospondin 9 (ADAMTS9) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.313-20ng/mL The standard curve concentrations used for the ELISA's were 20ng/mL, 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL. The minimum detectable dose of this kit is typically less than 0.109ng/mL 96-well strip plate SEK209Hu
Abl Interactor 1 (ABI1) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human Abl Interactor 1 (ABI1) No significant cross-reactivity or interference between Abl Interactor 1 (ABI1) and analogues was observed.. 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 Abl Interactor 1 (ABI1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Abl Interactor 1 (ABI1). 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 Abl Interactor 1 (ABI1), 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 Abl Interactor 1 (ABI1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.055ng/mL 96-well strip plate SEJ696Hu
Abscisic Acid (ABA) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Abscisic Acid (ABA) No significant cross-reactivity or interference between Abscisic Acid (ABA) and analogues was observed.. This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific for Abscisic Acid (ABA) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between Horseradish Peroxidase (HRP) labeled Abscisic Acid (ABA) and unlabeled Abscisic Acid (ABA) (Standards or samples) with the pre-coated antibody specific for Abscisic Acid (ABA). After incubation the unbound conjugate is washed off. The amount of bound HRP conjugate is reverse proportional to the concentration of Abscisic Acid (ABA) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Abscisic Acid (ABA) in the sample.. Sample Types: Tissue or cell culture supernates.. Detection Range: 1.23-100ng/mL The standard curve concentrations used for the ELISA's were 100ng/mL, 33.33ng/mL, 11.11ng/mL, 3.7ng/mL, 1.23ng/mL. The minimum detectable dose of this kit is typically less than 0.51ng/mL 96-well strip plate CEB218Ge
Absent In Melanoma 2 (AIM2) ELISA Kit This assay has high sensitivity and excellent specificity for detection of Human Absent In Melanoma 2 (AIM2) No significant cross-reactivity or interference between Absent In Melanoma 2 (AIM2) and analogues was observed.. 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 Absent In Melanoma 2 (AIM2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Absent In Melanoma 2 (AIM2). 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 Absent In Melanoma 2 (AIM2), 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 Absent In Melanoma 2 (AIM2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.. Sample Types: Serum, plasma, tissue homogenates, cell lysates and other biological fluids.. Detection Range: 0.156-10ng/mL The standard curve concentrations used for the ELISA's were 10ng/mL, 5ng/mL, 2.5ng/mL, 1.25ng/mL, 0.625ng/mL, 0.313ng/mL, 0.156ng/mL. The minimum detectable dose of this kit is typically less than 0.059ng/mL 96-well strip plate SEG302Hu
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