Transduction du signal

Anti-ANXA2 Antibody (7N216) is a Mouse antibody targeting ANXA2. Anti-ANXA2 Antibody (7N216) can be used in ELISA, WB, IHC.

Anti-ANXA2 Antibody (7P81) is an antibody targeting ANXA2. Anti-ANXA2 Antibody (7P81) can be used in ELISA, WB, IHC.

Anti-ANXA1 Antibody (3E707) is an antibody targeting ANXA1. Anti-ANXA1 Antibody (3E707) can be used in ELISA, IHC, FCM.

Anti-ITGB1 Antibody (3S449) is an antibody targeting ITGB1. Anti-ITGB1 Antibody (3S449) can be used in ELISA, WB, IHC, IF, FCM.

Anti-OCLN Antibody (2G215) is an antibody targeting OCLN. Anti-OCLN Antibody (2G215) can be used in ELISA, IHC, FCM.

Anti-Phospho-MAP2K1 (Thr292) Antibody (7K602) is an antibody targeting Phospho-MAP2K1 (Thr292). Anti-Phospho-MAP2K1 (Thr292) Antibody (7K602) can be used in ELISA, WB.

Anti-Phospho-PPP2CA (Tyr307) Antibody (7S944) is an antibody targeting Phospho-PPP2CA (Tyr307). Anti-Phospho-PPP2CA (Tyr307) Antibody (7S944) can be used in ELISA, WB.

Anti-STIP1 Antibody (2G123) is an antibody targeting STIP1. Anti-STIP1 Antibody (2G123) can be used in ELISA, WB.

Anti-MYLK Antibody (1O485) is an antibody targeting MYLK. Anti-MYLK Antibody (1O485) can be used in ELISA, WB, FCM.

Anti-WNK1 Antibody (1O394) is an antibody targeting WNK1. Anti-WNK1 Antibody (1O394) can be used in ELISA, IHC.

Anti-PLEKHA1 Antibody (8U160) is an antibody targeting PLEKHA1. Anti-PLEKHA1 Antibody (8U160) can be used in ELISA, WB.

Anti-AGBL2 Antibody (7X394) is a Mouse antibody targeting AGBL2. Anti-AGBL2 Antibody (7X394) can be used in ELISA, WB.

Anti-Phospho-AKT1 (Ser473) Antibody (5C817) is an antibody targeting Phospho-AKT1 (Ser473). Anti-Phospho-AKT1 (Ser473) Antibody (5C817) can be used in ELISA, WB, IHC, IF, IP.

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 PSA, and the Human PSA standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human PSA. After TMB substrate solution is added, only those wells that contain Human PSA and HRP-conjugated antibody 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 PSA 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 VASP, and the Human VASP standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human VASP. After TMB substrate solution is added, only those wells that contain Human VASP and HRP-conjugated antibody 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 VASP 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 PSMA, and the Human PSMA standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human PSMA. After TMB substrate solution is added, only those wells that contain Human PSMA and HRP-conjugated antibody 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 PSMA 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 VEGFR2, and the Human VEGFR2 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human VEGFR2. After TMB substrate solution is added, only those wells that contain Human VEGFR2 and HRP-conjugated antibody 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 VEGFR2 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 NLRP3, and the Human NLRP3 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human NLRP3. After TMB substrate solution is added, only those wells that contain Human NLRP3 and HRP-conjugated antibody 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 NLRP3 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 Rat vWF, and the Rat vWF standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Rat vWF. After TMB substrate solution is added, only those wells that contain Rat vWF and HRP-conjugated antibody 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 vWF 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 VEGFR2, and the Mouse VEGFR2 standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Mouse VEGFR2. After TMB substrate solution is added, only those wells that contain Mouse VEGFR2 and HRP-conjugated antibody 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 VEGFR2 in the samples is then determined by comparing the OD of the samples to the standard curve.