Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JE64-36 |
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: 74 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human RAVER2 aa 442-691/691. |
Positive control: | 293T cell lysates, human cervix carcinoma tissue. |
Subcellular location: | Cytoplasm, Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:400 |
Uniprot #: | SwissProt: Q9HCJ3 Human |
Alternative names: | DKFZp762D1011 FLJ10770 KIAA1579 Protein raver 2 Protein raver-2 Raver2 RAVR2_HUMAN Ribonucleoprotein PTB binding 2 Ribonucleoprotein PTB-binding 2 |
Fig1:
Western blot analysis of RAVER2 on 293T cell lysates with Rabbit anti-RAVER2 antibody (HA721100) at 1/1,000 dilution. Lysates/proteins at 10 µg/Lane.2 Predicted band size: 74 kDa Observed band size: 74 kDa Exposure time: 2 minutes; 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 (HA721100) at 1/1,000 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. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded human cervix carcinoma tissue with Rabbit anti-RAVER2 antibody (HA721100) at 1/400 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 (HA721100) at 1/400 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. |