Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 137/80 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human DIAPH3 aa 1,059-1,108 / 1,193. |
Positive control: | A431, LOVO, SiHa, human kidney tissue, human placenta tissue. |
Subcellular location: | Cytoplasm, Nucleus. |
Recommended Dilutions:
IF-Cell IHC-P FC WB |
1:50-1:200 1:50-1:400 1:50-1:100 1:500 |
Uniprot #: | SwissProt: Q9NSV4 Human | Q9Z207 Mouse |
Alternative names: | AN AUNA1 Dia2 diap3 DIAP3_HUMAN DIAPH3 Diaphanous homolog 3 (Drosophila) Diaphanous homolog 3 Diaphanous related formin 3 Diaphanous, Drosophila, homolog of, 3 Diaphanous-related formin-3 DKFZp434C0931 DKFZp686A13178 DRF3 FLJ34705 mDia2 NSDAN OTTHUMP00000018480 Protein diaphanous homolog 3 RP11-26P21.1 |
Fig1: Western blot analysis of DIAPH3 on SiHa cell lysate using anti-DIAPH3 antibody at 1/500 dilution. | |
Fig2: ICC staining DIAPH3 in LOVO cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig3: ICC staining DIAPH3 in SiHa cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig4: ICC staining DIAPH3 in A431 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig5:
Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-DIAPH3 antibody (ER1802-54) at 1/400 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 (ER1802-54) 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. |
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Fig6:
Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-DIAPH3 antibody (ER1802-54) at 1/400 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 (ER1802-54) 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. |
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Fig7: Flow cytometric analysis of LOVO cells with DIAPH3 antibody at 1/100 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti-rabbit IgG was used as the secondary antibody. |