RICTOR Recombinant Rabbit Monoclonal Antibody [1A5]
cat.: HA721142
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
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
Images
HA721142_1.jpg 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.
HA721142_2.jpg 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.
HA721142_3.jpg 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.
HA721142_4.jpg 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).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.