Mouse CXCL16 Recombinant Rabbit Monoclonal Antibody - BSA and Azide free (Detector) [PSH17-72] (HA723941)
Catalog# HA723941
Rabbit Monoclonal to CXCL16
Tested for
-
ELISA(Det)
Reacts with
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Mouse
Recombinant production enables lot-to-lot consistency and is animal-cruelty-free
Sandwich ELISA analysis of Mouse CXCL16 matched pair antibodies
Capture: HA723940, Mouse CXCL16 Rabbit mAb [PSH17-71]
Detector: HA723941, Mouse CXCL16 Rabbit mAb [PSH17-72]
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723940) diluted in carbonate/bicarbonate buffer, at a concentration of 2ug/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 Mouse CXCL16 protein (HA211059) starting from 4000 pg/ml to 0 pg/ml and detect antibody (HA723941, 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.
Capture: HA723940, Mouse CXCL16 Rabbit mAb [PSH17-71]
Detector: HA723941, Mouse CXCL16 Rabbit mAb [PSH17-72]
Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723940) diluted in carbonate/bicarbonate buffer, at a concentration of 2ug/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 Mouse CXCL16 protein (HA211059) starting from 4000 pg/ml to 0 pg/ml and detect antibody (HA723941, 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.