DIAPH3 Rabbit Polyclonal Antibody
cat.: ER1802-54
Product Type: Rabbit polyclonal IgG, primary antibodies
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
Images
ER1802-54_1.jpg Fig1: Western blot analysis of DIAPH3 on SiHa cell lysate using anti-DIAPH3 antibody at 1/500 dilution.
ER1802-54_2.jpg 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.
ER1802-54_3.jpg 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.
ER1802-54_4.jpg 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.
ER1802-54_5.png 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.
ER1802-54_6.png 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.
ER1802-54_7.jpg 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.