Sistema cardiovascolare

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

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat NMU. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NMU. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 NMU in the samples is then determined by comparing the OD of the samples to the standard curve.

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 Rabbit ANG1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rabbit ANG1. 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 Rabbit ANG1, 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 Rabbit ANG1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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 P4HTM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human P4HTM. 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 P4HTM, 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 P4HTM in the samples is then determined by comparing the OD of the samples to the standard curve.

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

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

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with PGF2a. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PGF2a. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 PGF2a in the samples is then determined by comparing the OD of the samples to the standard curve.

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

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Dog ANP. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Dog ANP. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 ANP in the samples is then determined by comparing the OD of the samples to the standard curve.

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

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Chicken DA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Chicken DA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Chicken DA in the samples is then determined by comparing the OD of the samples to the standard curve.

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 GLUT4. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human GLUT4. 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 GLUT4, 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 GLUT4 in the samples is then determined by comparing the OD of the samples to the standard curve.

A unique collection of xnum GPCR-active agents for high throughput screening and high content screening for GPCR drug discovery, and new GPCR target

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2-Hydroxybenzylamine captures IsoLGs, prevents early atrial fibrillation recurrence post-ablation.

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Regaloside C is a glycerol glucoside isolated from Lilium genus with anti-inflammatory properties.

Sirtuin modulator 2 (N-(3-(imidazo[2,1-b]thiazol-6-yl)phenyl)-2-methoxybenzamide) exhibits antidiabetic, anti-inflammatory and antitumor activities.

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A unique collection of 1336 HIF-1 related small chemicals can be used for drug discovery in ischemic disease and cancer and related mechanism studies；

A unique collection of 1353 proangiogenic and antiangiogenic compounds for new targets identification, research in mechanisms of angiogenesis, and high

Anti-FABP3 Antibody (7D420) is a Mouse antibody targeting FABP3. Anti-FABP3 Antibody (7D420) can be used in ELISA, WB, IHC.

Anti-GLA/alpha-Galactosidase A Antibody (3E14) is an antibody targeting GLA/alpha-Galactosidase A. Anti-GLA/alpha-Galactosidase A Antibody (3E14) can be used in ELISA, IHC, FCM.

Anti-FABP4 Antibody (6E726) is an antibody targeting FABP4. Anti-FABP4 Antibody (6E726) can be used in ELISA.

Anti-Coagulation factor X/F10 Antibody (5F696) is an antibody targeting Coagulation factor X/F10. Anti-Coagulation factor X/F10 Antibody (5F696) can be used in ELISA, IHC.

Anti-Glycophorin A Antibody (2S153) is an antibody targeting Glycophorin A. Anti-Glycophorin A Antibody (2S153) can be used in ELISA, FCM.

Anti-IL-8/CXCL8 Antibody (5C84) is a Mouse antibody targeting IL-8/CXCL8. Anti-IL-8/CXCL8 Antibody (5C84) can be used in ELISA, IHC.

Anti-Haptoglobin Antibody (4J724) is an antibody targeting Haptoglobin. Anti-Haptoglobin Antibody (4J724) can be used in ELISA, IHC.

Anti-CD9 Antibody (6U52) is an antibody targeting CD9. Anti-CD9 Antibody (6U52) can be used in ELISA, WB, IHC, IF, FCM.

Anti-CETP Antibody (2H481) is an antibody targeting CETP. Anti-CETP Antibody (2H481) can be used in ELISA, IHC.

Anti-CD9 Antibody (5F780) is a Mouse antibody targeting CD9. Anti-CD9 Antibody (5F780) can be used in ELISA, WB.

Anti-CD31 Antibody (6V47) is an antibody targeting CD31. Anti-CD31 Antibody (6V47) can be used in ELISA, WB, IHC, FCM.

Anti-SAA1 Antibody (5E204) is a Mouse antibody targeting SAA1. Anti-SAA1 Antibody (5E204) can be used in ELISA.

Anti-Phospho-PTK2 (Tyr397) Antibody (5N156) is an antibody targeting Phospho-PTK2 (Tyr397). Anti-Phospho-PTK2 (Tyr397) Antibody (5N156) can be used in ELISA, WB.

Anti-Carbonic Anhydrase 9 Antibody (8S986) is an antibody targeting Carbonic Anhydrase 9. Anti-Carbonic Anhydrase 9 Antibody (8S986) can be used in ELISA, IHC.

Anti-Serum albumin Antibody (3I761) is a Mouse antibody targeting Serum albumin. Anti-Serum albumin Antibody (3I761) can be used in ELISA, WB.

Anti-Phospho-PDGFRB (Tyr740) Antibody (9D509) is an antibody targeting Phospho-PDGFRB (Tyr740). Anti-Phospho-PDGFRB (Tyr740) Antibody (9D509) can be used in ELISA, WB.

Anti-CD63 Antibody (2H536) is an antibody targeting CD63. Anti-CD63 Antibody (2H536) can be used in ELISA, IHC, IF.

Anti-Osteopontin Antibody (6U756) is a Mouse antibody targeting Osteopontin. Anti-Osteopontin Antibody (6U756) can be used in ELISA, WB, IHC.

Antibody Type: Mouse Monoclonal
Application: ELISA,IHC
Reactivity: Human

Anti-AMBP Antibody (8J942) is a Mouse antibody targeting AMBP. Anti-AMBP Antibody (8J942) can be used in ELISA, IHC.

Anti-ANGPT2/Angiopoietin-2 Antibody (6U152) is an antibody targeting ANGPT2/Angiopoietin-2. Anti-ANGPT2/Angiopoietin-2 Antibody (6U152) can be used in ELISA, IHC.

Anti-Adiponectin Antibody (6G540) is a Mouse antibody targeting Adiponectin. Anti-Adiponectin Antibody (6G540) can be used in ELISA.