Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, IF-Cell |
Clonality: | Monoclonal |
Clone number: | JM66-31 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 125 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within N-terminal human JAK3. |
Positive control: | Hela, human spleen tissue, human tonsil tissue. |
Subcellular location: | Endomembrane system, Cytoplasm. |
Recommended Dilutions:
WB IHC-P IF-Cell |
1:500 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P52333 Human |
Alternative names: | EC 2.7.10.2 JAK 3 JAK L JAK-3 Jak3 JAK3 HUMAN JAK3_HUMAN JAKL Janus kinase 3 (a protein tyrosine kinase, leukocyte) Janus kinase 3 Janus Kinase3 L JAK L-JAK Leukocyte janus kinase LJAK Protein tyrosine kinase leukocyte Tyrosine protein kinase JAK3 Tyrosine-protein kinase JAK3 |
Fig1: ICC staining of JAK3 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1705-1, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). | |
Fig2: Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-JAK3 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-1, 1/50) for 30 minutes 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-JAK3 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1705-1, 1/50) for 30 minutes 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. |