domestic rabbit monoclonal (PSH17-46)
reactivity: human
application: ELISA
reactivity: human
application: ELISA
Sandwich ELISA analysis of Human CXADR matched pair antibodies Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA725293) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Human CXADR protein (HA211206) starting from 3,000 pg/ml to 0 pg/ml and detect antibody (HA725294, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Interpolated concentrations of native CXADR in A549 and K-562 Cell extract samples based on a 1,000 µg/ml extract load. Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Interpolated concentration of native CXADR was measured in duplicate at different sample concentrations. The interpolated dilution factor corrected values were plotted (mean +/- SD, n=2). The mean CXADR concentration was determined to be 8,412 pg/mL in HeLa Cell extract and undetectable in K-562 Cell extract.
quantity: 100μl
price: 649.00 USD
to the supplier
domestic rabbit monoclonal (PSH17-47)
reactivity: human
application: ELISA
reactivity: human
application: ELISA
Sandwich ELISA analysis of Human CXADR matched pair antibodies Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA725293) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Human CXADR protein (HA211206) starting from 3,000 pg/ml to 0 pg/ml and detect antibody (HA725294, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Interpolated concentrations of native CXADR in A549 and K-562 Cell extract samples based on a 1,000 µg/ml extract load. Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Interpolated concentration of native CXADR was measured in duplicate at different sample concentrations. The interpolated dilution factor corrected values were plotted (mean +/- SD, n=2). The mean CXADR concentration was determined to be 8,412 pg/mL in HeLa Cell extract and undetectable in K-562 Cell extract.
quantity: 100μl
price: 649.00 USD
to the supplier
domestic rabbit monoclonal (PSH17-47)
reactivity: human
conjugate: biotin
application: ELISA
reactivity: human
conjugate: biotin
application: ELISA
Sandwich ELISA analysis of Human CXADR matched pair antibodies Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA725293) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Human CXADR protein (HA211206) starting from 3,000 pg/ml to 0 pg/ml and detect antibody (HA725294, Biotin, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Then the plate was washed and incubated with 100 µl per well of SA-HRP for 0.5 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
Interpolated concentrations of native CXADR in A549 and K-562 Cell extract samples based on a 1,000 µg/ml extract load. Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Interpolated concentration of native CXADR was measured in duplicate at different sample concentrations. The interpolated dilution factor corrected values were plotted (mean +/- SD, n=2). The mean CXADR concentration was determined to be 8,412 pg/mL in HeLa Cell extract and undetectable in K-562 Cell extract.
quantity: 100μl
price: 409.00 USD
to the supplier
domestic rabbit monoclonal (PSH17-47)
reactivity: human
conjugate: HRP
application: ELISA
reactivity: human
conjugate: HRP
application: ELISA
Sandwich ELISA analysis of Human CXADR matched pair antibodies Capture: HA725293, Human CXADR Rabbit mAb [PSH17-46] Detector: HA725294, Human CXADR Rabbit mAb [PSH17-47] Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA725293) diluted in carbonate/bicarbonate buffer, at a concentration of 2 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with 150 µl 0.05% tween-20 1% BSA blocking buffer, and incubated with serial diluted Recombinant Human CXADR protein (HA211206) starting from 20,000 pg/ml to 0 pg/ml and detect antibody (HA725294, HRP, 0.2 µg/ml) for 1 hour at 30℃ with shaking. Detection was performed using an Ultra TMB Substrate for 10 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.
quantity: 100μl
price: 385.00 USD
to the supplier