Prohibitin(Mitochondrial Marker) Rabbit Polyclonal Antibody
cat.: R1510-30
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 30kDa
Isotype: IgG
Immunogen: Synthetic peptide within C-terminal human Prohibitin.
Positive control: Hela, HepG2, C2C12, F9, PC12, Jurkat, human kidney tissue, mouse liver tissue, human liver carcinoma tissue, mouse kidney tissue, mouse heart tissue.
Subcellular location: Mitochondrion inner membrane, Nucleus, Cytoplasm, Cell membrane.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:1,000-1:2,000
1:50-1:200
1:50-1:200
1:500-1:1,000
Uniprot #: SwissProt: P35232 Human | P67778 Mouse | P67779 Rat
Alternative names: Epididymis luminal protein 215 Epididymis secretory sperm binding protein Li 54e HEL 215 HEL S 54e PHB PHB_HUMAN PHB1 Prohibitin
Images
R1510-30_1.jpg Fig1: Western blot analysis on different cell lysates using anti-Prohibitin rabbit polyclonal antibody. Positive control:
Lane 1: F9
Lane 2: Jurkat
Lane 3: Mouse kidney
Lane 4: PC-12
R1510-30_2.jpg Fig2: Immunocytochemical staining of Hela cells using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_3.jpg Fig3: Immunocytochemical staining of HepG2 cells using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_4.jpg Fig4: Immunocytochemical staining of C2C12 cells using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-Prohibitin(Mitochondrial Marker) antibody (R1510-30) 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 (R1510-30) 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.
R1510-30_6.jpg Fig6: Immunohistochemical analysis of paraffin- embedded human kidney tissue using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-Prohibitin(Mitochondrial Marker) antibody (R1510-30) 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 (R1510-30) 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.
R1510-30_8.jpg Fig8: Immunohistochemical analysis of paraffin- embedded mouse kidney tissue using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_9.jpg Fig9: Immunohistochemical analysis of paraffin- embedded mouse heart tissue using anti-Prohibitin rabbit polyclonal antibody.
R1510-30_10.jpg Fig10: Flow cytometric analysis of HepG2 cells labeling Prohibitin(Mitochondrial Marker).

Cells were fixed and permeabilized. Then stained with the primary antibody (R1510-30, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.