Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE57-62 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: 58 kDa. |
Isotype: | IgG |
Immunogen: | Recombinant protein within human EGR1 aa 1-200. |
Positive control: | SW480 cell lysates, human thyroid carcinoma tissue. |
Subcellular location: | Nucleus, Cytoplasm. |
Recommended Dilutions:
WB IHC-P |
1:500-1:2,000 1:50-1:200 |
Uniprot #: | SwissProt: P18146 Human |
Alternative names: | AT225 Early growth response 1 Early growth response protein 1 EGR 1 EGR-1 EGR1 EGR1_HUMAN G0S30 KROX 24 KROX24 Nerve growth factor-induced clone A Nerve growth factor-induced protein A NGFI-A NGFIA TIS8 Transcription factor ETR103 Transcription factor Zif268 ZIF 268 ZIF268 Zinc finger protein 225 Zinc finger protein Krox-24 ZNF225 |
Fig1: Western blot analysis of EGR1 on SW480 cell lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET7111-41, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. | |
Fig2:
Immunohistochemical analysis of paraffin-embedded human thyroid carcinoma tissue with Rabbit anti-EGR1 antibody (ET7111-41) at 1/800 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7111-41) at 1/800 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. |