LAG-3 Recombinant Rabbit Monoclonal Antibody [PSH0-43]
cat.: HA721345
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: PSH0-43
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 57.4 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human LAG-3 aa 1-500 / 525.
Positive control: NIH/3T3 transfected with LAG3 cell lysate, human tonsil tissue.
Subcellular location: Cell membrane; Secreted.
Recommended Dilutions:
  WB
  IHC-P

1:2,000
1:200
Uniprot #: SwissProt: P18627 Human | Q61790 Mouse
Alternative names: CD223 CD223 antigen FDC protein LAG-3 Lag3 LAG3_HUMAN Lymphocyte activating 3 Lymphocyte activation gene 3 Lymphocyte activation gene 3 protein Protein FDC
Images
HA721345_1.jpg Fig1: Western blot analysis of LAG-3 on different lysates with Rabbit anti-LAG-3 antibody (HA721345) at 1/2,000 dilution.

Lane 1: NIH/3T3 transfected with LAG3 expression vector, whole cell lysate
Lane 2: NIH/3T3 cell lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 57.4 kDa
Observed band size: 55/70 kDa

Exposure time: 1 minute 10 seconds;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721345) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
HA721345_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-LAG-3 antibody (HA721345) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721345) at 1/200 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.