Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | IHC-P |
Clonality: | Monoclonal |
Clone number: | PD00-48 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 60 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide. |
Positive control: | Human colon carcinoma tissue, human ovary carcinoma tissue. |
Subcellular location: | Nucleus, Cytoplasm, Mitochondrion, Cell projection. |
Recommended Dilutions:
IHC-P |
1:1,000 |
Uniprot #: | SwissProt: O94763 Human |
Alternative names: | C19orf2 Chromosome 19 open reading frame 2 NNX3 NNX3 protein PPP1R19 Protein NNX3 Protein phosphatase 1 regulatory subunit 19 RMP RMP_HUMAN RNA polymerase II subunit 5 mediating protein RNA polymerase II subunit 5-mediating protein RPB5 mediating protein RPB5-mediating protein Unconventional prefoldin RPB5 interactor 1 Unconventional prefoldin RPB5 interactor URI URI1 URI1, prefoldin-like chaperone |
Fig1:
Immunohistochemical analysis of paraffin-embedded human colon carcinoma tissue with Rabbit anti-C19orf2 antibody (HA721196) at 1/1,000 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 (HA721196) at 1/1,000 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. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded human ovary carcinoma tissue with Rabbit anti-C19orf2 antibody (HA721196) at 1/1,000 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 (HA721196) at 1/1,000 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. |