Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Monoclonal |
Clone number: | JG96-30 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. 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: 52 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human FKBP52 aa 1-132 / 459. |
Positive control: | SK-Br-3 cell lysate, HeLa cell lysate, Mouse testis tissue lysate, Rat testis tissue lysate, human prostate cancer tissue, 293T, MCF-7. |
Subcellular location: | Cytoplasm. Cytoskeleton. Microtubule. Mitochondrion. Nucleus. |
Recommended Dilutions:
WB IF-Cell IHC-P FC |
1:2,000 1:50-1:200 1:1,000 1:1,000 |
Uniprot #: | SwissProt: Q02790 Human | P30416 Mouse | Q9QVC8 Rat |
Alternative names: | 51 kDa FK506-binding protein 52 kDa FK506 binding protein 52 kDa FK506-binding protein 52 kDa FKBP 59 kDa immunophilin FK506 binding protein 4 FK506-binding protein 4 FKBP 4 FKBP 52 FKBP 59 FKBP-4 FKBP-52 FKBP4 FKBP4_HUMAN FKBP51 FKBP52 protein FKBP59 HBI Hsp 56 HSP binding immunophilin HSP-binding immunophilin Hsp56 Immunophilin FKBP52 N-terminally processed p52 p59 p59 protein Peptidyl prolyl cis trans isomerase Peptidyl-prolyl cis-trans isomerase FKBP4 Peptidylprolyl cis trans isomerase PPIase PPIase FKBP4 Rotamase T cell FK506 binding protein 59kD |
Fig1:
Western blot analysis of FKBP52 on different lysates with Rabbit anti-FKBP52 antibody (ET7108-93) at 1/2,000 dilution. Lane 1: SK-Br-3 cell lysate (20 µg/Lane) Lane 2: HeLa cell lysate (20 µg/Lane) Lane 3: Mouse testis tissue lysate (40 µg/Lane) Lane 3: Rat testis tissue lysate (40 µg/Lane) Predicted band size: 52 kDa Observed band size: 55 kDa Exposure time: 25 seconds; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET7108-93) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded human prostate cancer tissue with Rabbit anti-FKBP52 antibody (ET7108-93) at 1/1,000 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 (ET7108-93) 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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Fig3: ICC staining FKBP52 in 293T cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig4: ICC staining FKBP52 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig5:
Flow cytometric analysis of 293T cells labeling FKBP52. Cells were fixed and permeabilized. Then stained with the primary antibody (ET7108-93, 1/1,000) (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). |