Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IHC-P, IF-Cell, FC |
Clonality: | Monoclonal |
Clone number: | 1A5 |
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: 192 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human RICTOR aa 1459-1708 / 1708. |
Positive control: | HepG2 cell lysates, mouse liver tissue, A431, Hela. |
Subcellular location: | Cytosol, TORC2 complex. |
Recommended Dilutions:
WB IHC-P IF-Cell FC |
1:500 1:500 1:100 1:500-1:1,000 |
Uniprot #: | SwissProt: Q6R327 Human | Q6QI06 Mouse |
Alternative names: | AVO3 AVO3 homolog DKFZp686B11164 hAVO3 KIAA1999 Likely ortholog of mouse TORC2 specific protein AVO3 (S. cerevisiae) mAVO3 MGC39830 PIA Pianissimo Rapamycin insensitive companion of mTOR Rapamycin-insensitive companion of mTOR Rictor RICTR RICTR_HUMAN RPTOR independent companion of MTOR complex 2 TORC2 specific protein AVO3 |
Fig1:
Western blot analysis of RICTOR on HepG2 cell lysates with Rabbit anti-RICTOR antibody (HA721142) at 1/500 dilution. Lysates/proteins at 10 µg/Lane. Predicted band size: 192 kDa Observed band size: 192 kDa Exposure time: 2 minutes; 6% 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 (HA721142) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-RICTOR antibody (HA721142) at 1/500 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 (HA721142) at 1/500 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:
Immunocytochemistry analysis of A431 cells labeling RICTOR with Rabbit anti-RICTOR antibody (HA721142) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-RICTOR antibody (HA721142) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. |
Fig4:
Flow cytometric analysis of Hela cells labeling RICTOR. Cells were fixed and permeabilized. Then stained with the primary antibody (HA721142, 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). |