| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | ELISA(Det) |
| Clonality: | Monoclonal |
| Clone number: | PSH09-82 |
| Form: | Liquid |
| Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term. |
| Storage buffer: | 1*PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclean 950. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Isotype: | IgG |
| Immunogen: | Recombinant protein within Human PD-L2 Protein aa 20-220 (HA210599) |
| Positive control: | Recombinant Human PD-L2 Protein (HA210599). |
| Subcellular location: | Cell membrane, Secreted. |
| Recommended Dilutions:
ELISA(Det) |
Use at an assay dependent concentration. Can be paired for Sandwich ELISA with Rabbit monoclonal [PSH09-80] to Human PD-L2 antibody (Capture) (HA723145) or Rabbit monoclonal [PSH09-81] to Human PD-L2 antibody (Capture) (HA723146) and Recombinant Human PD-L2 protein (HA210599) as the standard. |
| Uniprot #: | SwissProt: Q9BQ51 Human |
| Alternative names: | B7 dendritic cell molecule B7-DC B7DC bA574F11.2 Btdc Butyrophilin B7 DC Butyrophilin B7-DC Butyrophilin B7DC CD 273 CD273 CD273 antigen MGC142238 MGC142240 PD 1 ligand 2 PD L2 PD-1 ligand 2 PD-L2 PD1 ligand 2 PD1L2_HUMAN PDCD 1 ligand 2 PDCD1 ligand 2 PDCD1L2 Pdcd1lg2 PDL 2 PDL2 Programmed cell death 1 ligand 2 Programmed death ligand 2 |
|
Fig1:
Sandwich ELISA analysis of Human PD-L2 matched pair antibodies Elisa assay was performed by coating wells of a 96-well plate with 100 µl per well of capture antibody (HA723146) diluted in carbonate/bicarbonate buffer, at a concentration of 0.5ug/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 PD-L2 (HA210599) starting from 111.11 ng/ml to 0 ng/ml and detect antibody (HA723373H, HRP, 0.01 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. |