FOXP1 Recombinant Rabbit Monoclonal Antibody [JF1017]
cat.: ET1702-44
| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse, Rat |
| Applications: | WB, IHC-P, FC |
| Clonality: | Monoclonal |
| Clone number: | JF1017 |
| Form: | Liquid |
| Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term. |
| 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: | 77/75 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within human FOXP1 aa 615-653 / 677. |
| Positive control: | Hela cell lysate, Jurkat cell lysate, MCF-7 cell lysate, human colon carcinoma tissue, human breast carcinoma tissue, MCF-7. |
| Subcellular location: | Nucleus. |
| Recommended Dilutions:
WB FC IHC-P |
1:1,000-1:5,000 1:50-1:100 1:50-1:200 |
| Uniprot #: | SwissProt: Q9H334 Human | P58462 Mouse | Q498D1 Rat |
| Alternative names: | 12CC4 FLJ23741 Fork head related protein like B Forkhead box P1 Forkhead box protein P1 FOX P1 FOXP 1 foxp1 FOXP1_HUMAN Glutamine rich factor 1 hFKH1B HSPC215 MGC12942 MGC88572 MGC99551 QRF 1 QRF1 |
Images
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Fig1: Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue using anti-FOXP1 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1702-44, 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. |
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Fig2: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-FOXP1 antibody. 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 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1702-44, 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. |
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Fig3: Flow cytometric analysis of FOXP1 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1702-44, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
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Fig4:
Western blot analysis of FOXP1 on Jurkat cell lysates with Rabbit anti-FOXP1 antibody (ET1702-44) at 1/5,000 dilution. Lysates/proteins at 15 µg/Lane. Exposure time: 1 minutes; ECL: K1801 Blocking: 5% NFDM/TBST, 1 hour at room temperature Primary antibody: ET1702-44, 1/5,000 in primary antibody dilution buffer (K1803), overnight at 4 ℃ Secondary antibody: Goat anti-Rabbit IgG-HRP (HA1001), 1/50,000 in 5% NFDM/TBST, 1 hour at room temperature Predicted band size: 75.3 kDa Observed band size: 75/77 kDa |
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.