Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P, IP |
Clonality: | Monoclonal |
Clone number: | JA10-32 |
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: | 43 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human GATA1 aa 1-250. |
Positive control: | K562 cell lysates, human breast carcinoma tissue, human liver tissue, human kidney tissue. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:500-1:1,000 1:50-1:200 |
Uniprot #: | SwissProt: P15976 Human |
Alternative names: | Anemia, X-linked, without thrombocytopenia, included ERYF 1 Eryf1 Erythroid transcription factor Erythrold transcription factor 1 GATA 1 GATA binding factor 1 GATA binding protein 1 (globin transcription factor 1) GATA binding protein 1 GATA-1 GATA-binding factor 1 GATA1 GATA1_HUMAN GF 1 GF-1 GF1 Globin transcription factor 1 NF E1 NF E1 DNA binding protein NF-E1 DNA-binding protein NFE 1 NFE1 Nuclear factor erythroid 1 Transcription factor GATA1 XLANP XLTDA XLTT |
Fig1:
Western blot analysis of GATA1 on K562 cell lysates with Rabbit anti-GATA1 antibody (ET1704-41) at 1/500 dilution. Lysates/proteins at 10 µg/Lane. Predicted band size: 43 kDa Observed band size: 50 kDa Exposure time: 30 seconds; 10% 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 (ET1704-41) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig2: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-GATA1 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-41, 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 liver tissue using anti-GATA1 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-41, 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. |
Fig4: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-GATA1 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-41, 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. |