Anti-PD-L2 Antibody (2N448) is a Mouse antibody targeting PD-L2. Anti-PD-L2 Antibody (2N448) can be used in ELISA, WB, IHC, IF, FCM, IP.

IgG2b

2N448

Human

1. Western Blot
-Positive WB detected in: HepG2 whole cell lysate, Hela whole cell lysate, PC-3 whole cell lysate, A549 whole cell lysate
-All lanes PD-L2 antibody at 1:2000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 31,21 KDa
-Observed band size: 45-50 KDa
-Exposure time:5min
2. Western Blot
-Positive WB detected in: Hela whole cell lysate at 20μg, 10μg, 5μg, 2.5μg, 1.25μg
-All lanes: PD-L2 antibody at 1:2000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 31,21 KDa
-Observed band size: 45-50 KDa
-Exposure time:5min
3. Western Blot
-Positive WB detected in: 15μg hela whole cell lysate PD-L2 antibody at 1:5000, 1:10000, 1:20000, 1:40000, 1:80000, 1:160000, 1:320000, 1:640000
-Secondary: Goat polyclonal to mouse IgG at 1/50000 dilution
-Predicted band size: 31,21 KDa
-Observed band size: 45-50 KDa
-Exposure time:5min
4. IHC image of TMAH-00872 diluted at 1:100 and staining in paraffin-embedded human tonsil tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
5. Immunofluorescence staining of HepG2 cells with TMAH-00872 at 1:100, counter-stained with DAPI. The cells were incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
6. Immunofluorescence staining of Hela cells with TMAH-00872 at 1:100, counter-stained with DAPI. The cells were incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
7. Immunofluorescence staining of Raji cells with TMAH-00872 at 1:100, counter-stained with DAPI. The cells were incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
8. Immunofluorescence staining of U251 cells with TMAH-00872 at 1:100, counter-stained with DAPI. The cells were incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
9. Overlay histogram showing 293 cells transfected with PD-L2 stained with TMAH-00872 (red line). The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (2µg/1*106cells) for 1 h at 4°C. The secondary antibody used was R-PE-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4°C. Isotype control antibody (green line) was mouse IgG2b (2µg/1*106cells) used under the same conditions. Acquisition of >10,000 events was performed.
10. Immunoprecipitating PD-L2 in Hela whole cell lysate
-Lane 1: Mouse control IgG instead of TMAH-00872 in Hela whole cell lysate
-Lane 2: TMAH-00872 (2µl) + Hela whole cell lysate (500µg)
-Lane 3: Hela whole cell lysate (20µg)
For western blotting, the blot was detected with TMAH-00872 at 1:2000, and a HRP-conjugated Protein G antibody was used as the secondary antibody at 1:2000

Monoclonal

Unconjugated

Recombinant Protein: Human Programmed cell death 1 ligand 2 Protein (21-118AA)

Human

Immunology