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RICTOR Recombinant Rabbit Monoclonal Antibody [1D5] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA750483

RICTOR Recombinant Rabbit Monoclonal Antibody [1D5] - BSA and Azide free

Application

  • WB

  • IF-Cell

  • FC

Reactivity

  • Human

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

RICTOR Recombinant Rabbit Monoclonal Antibody [1D5] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human RICTOR aa 1459-1708 / 1708.

Species Reactivity

Human

Validated Applications

WB, IF-Cell, FC

Target Molecular Weight

Predicted band size: 192 kDa

Positive Control

A549 cell lysate, SW480 cell lysate, A431, Hela.

Conjugation

unconjugated

Clone Number

1D5

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Rapamycin-insensitive companion of mammalian target of rapamycin (RICTOR) is a protein that in humans is encoded by the RICTOR gene. RICTOR and mTOR are components of a protein complex that integrates nutrient- and growth factor-derived signals to regulate cell growth. RICTOR is a subunit of the mammalian target of rapamycin complex 2 (mTORC2) which contains mTOR, GβL, RICTOR (this protein) and mSIN1. The mammalian target of rapamycin (mTOR) is a highly conserved Ser/Thr kinase that regulates cell growth and proliferation. mTOR may exist as mTOR complex 1 (mTORC1) or mTOR complex 2 (mTORC2). RICTOR is a key component of mTORC2, which, unlike mTORC1, is not directly inhibited by rapamycin. mTORC2, and RICTOR, specifically, has been shown to phosphorylate Akt/protein kinase B (PKB) on SER473. This phosphorylation activates Akt/PKB, where deregulation of Akt/PKB has been implicated in cancer and diabetes. RICTOR and mTORC2 have been shown to play an essential role in embryonic growth and development, perhaps due to the control that mTORC2 exerts on actin cytoskeleton organization. Diseases associated with mutation in the RICTOR gene include foramen magnum meningioma and syringomyelia. Akt/PMB activation is also involved in glucose metabolism and activation of Akt by RICTOR has been shown to mediate glucose and lipid metabolism. Therefore, the influence of RICTOR and mTORC2 on Akt signaling has been associated with insulin resistance and type 2 diabetes.

Background References

1. Ramaiah MJ. et. al. mTOR-Rictor-EGFR axis in oncogenesis and diagnosis of glioblastoma multiforme. Mol Biol Rep. 2021 May

2. Xu S. et. al. Rictor Is a Novel Regulator of TRAF6/TRAF3 in Osteoclasts. J Bone Miner Res. 2021 Oct

Subcellular Location

Cytosol, Golgi apparatus.

UNIPROT

SwissProt: Q6R327 Human

Synonyms

AVO3 antibody

AVO3 homolog antibody

DKFZp686B11164 antibody

hAVO3 antibody

KIAA1999 antibody

Likely ortholog of mouse TORC2 specific protein AVO3 (S. cerevisiae) antibody

mAVO3 antibody

MGC39830 antibody

PIA antibody

Pianissimo antibody

Expand

Images

  • This data was developed using <a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of RICTOR on different lysates with Rabbit anti-RICTOR antibody (<a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>) at 1/500 dilution.<br /><br />Lane 1: A549 cell lysate<br />Lane 2: SW480 cell lysate<br /><br />Lysates/proteins at 10 µg/Lane.<br /><br />Predicted band size: 192 kDa<br />Observed band size: 192 kDa<br /><br />Exposure time: 2 minutes;<br /><br />6% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1:300,000 dilution was used for 1 hour at room temperature.

    This data was developed using HA721141, the same antibody clone in a different buffer formulation.
    Western blot analysis of RICTOR on different lysates with Rabbit anti-RICTOR antibody (HA721141) at 1/500 dilution.

    Lane 1: A549 cell lysate
    Lane 2: SW480 cell lysate

    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 (HA721141) 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.

  • This data was developed using <a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of A431 cells labeling RICTOR with Rabbit anti-RICTOR antibody (<a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>) at 1/100 dilution.<br /><br />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 (<a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>) at 1/100 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 488, <a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) 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.

    This data was developed using HA721141, the same antibody clone in a different buffer formulation.
    Immunocytochemistry analysis of A431 cells labeling RICTOR with Rabbit anti-RICTOR antibody (HA721141) 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 (HA721141) 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.

  • This data was developed using <a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>, the same antibody clone in a different buffer formulation.<br />Flow cytometric analysis of Hela cells labeling RICTOR.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA721141" style="font-weight: bold;text-decoration: underline;">HA721141</a>, 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&trade; 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (<a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    This data was developed using HA721141, the same antibody clone in a different buffer formulation.
    Flow cytometric analysis of Hela cells labeling RICTOR.

    Cells were fixed and permeabilized. Then stained with the primary antibody (HA721141, 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).

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