Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JB38-41 |
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: 38 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human RING2 aa 83-256 . |
Positive control: | K562 cell lysate, human placenta tissue, human breast carcinoma tissue. |
Subcellular location: | Chromosome. Nucleus. |
Recommended Dilutions:
WB IHC-P |
1:500-1:1,000 1:50-1:1,000 |
Uniprot #: | SwissProt: Q99496 Human |
Alternative names: | BAP 1 BAP1 DING DinG protein E3 ubiquitin protein ligase RING 2 E3 ubiquitin protein ligase RING2 E3 ubiquitin-protein ligase RING2 HIP2 interacting protein 3 HIP2-interacting protein 3 HIPI 3 HIPI3 Huntingtin interacting protein 2 interacting protein 3 Huntingtin-interacting protein 2-interacting protein 3 OTTHUMP00000060668 Polycomb M33 interacting protein Ring 1B Polycomb M33 interacting protein Ring1B Protein DinG RING 1B RING 2 RING finger protein 1B RING finger protein 2 RING finger protein BAP 1 RING finger protein BAP-1 RING finger protein BAP1 RING1b RING2_HUMAN RNF 2 Rnf2 |
Fig1: Western blot analysis of RING2 on k562 cell using anti-RING2 antibody at 1/500 dilution. | |
Fig2: Immunohistochemical analysis of paraffin-embedded human placenta tissue using anti-RING2 antibody. Counter stained with hematoxylin. | |
Fig3:
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-RING2 antibody (ET7107-07) at 1/200 dilution. 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 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET7107-07) at 1/200 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. |