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Akt, also known as protein kinase B (PKB) or Rac, is a serine/threonine kinase that is of significant interest in pharmaceutical research due to its implicated roles in cell growth, cell survival, cancer, diabetes, and neurological disorders. Activated Akt promotes growth factor-mediated cell survival by inhibiting apoptosis through several signaling pathways. An anti-apoptotic effect of Akt overexpression has been observed in breast, pancreatic, and ovarian cancer cells. Akt also regulates glycogen synthesis and may play a role in glucose uptake following insulin stimulation. The central role of Akt signaling in multiple disease conditions has created a need for immunoassays that can accurately quantify this protein in biological samples. Such quantification can be obtained with an electrochemiluminescence assay by using recombinant protein standards as calibrators as opposed to the qualitative Western blot method. To enable the accurate measurement of active Akt, MSD has developed a Phospho-Akt (Ser473) Kit that uses purified protein calibrator and provides assay-specific components for the quantitative determination of endogenous Akt phosphorylated at serine 473 in human, mouse, rat, and non-human primate cell lysates and tissue lysates. This all-inclusive kit includes the MULTI-SPOT Akt Plate, Akt Calibrator, Anti-Phospho-Akt (Ser473) Antibody, Diluent 39, Tris Wash Buffer, Read Buffer T, inhibitors, and blockers. As supplementary materials, MSD also offers the Akt Control Pack I, which includes cell lysates at two concentrations, and an Inhibitor Pack, which contains phosphatase and protease inhibitors.
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Specifications
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Kit Contents
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Documentation
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References
Application(s)
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Phosphoproteins
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Intracellular Signaling
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Analyte(s)
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Akt
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Species
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Human, Mouse, Rat, Non-human primate
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Instrument(s)
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SECTOR Imager 2400
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MESO SECTOR S 600MM
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SECTOR Imager 6000
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MESO QuickPlex SQ 120MM
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MESO QuickPlex SQ 120
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MESO SECTOR S 600
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Plate Type
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96-well
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Capture Antibody
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Mouse Monoclonal
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Detection Antibody
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Mouse Monoclonal
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LLOD (Sensitivity)
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0.0050 UP473/well
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Dynamic Range
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0.0050-50 UP473/well
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Phospho relation sites
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pS473
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Recombinant standards
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Full length recombinant human Akt1, phosphorylated in vitro
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Usage Statement
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For Research Use Only. Not for use in diagnostic procedures.
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Storage Statement(s)
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Please refer to the product insert for the storage conditions of individual kit components.
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Storage Condition
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Multi-Component
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Schedule B Code
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3822.19.0000
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Product Description
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Storage
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Quantity per Kit
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Phosphatase Inhibitor I 0.1 mL
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2-8 °C
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1 each (0.1 mL)
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Phosphatase Inhibitor II 0.1 mL
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2-8 °C
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1 each (1 each)
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Protease Inhibitor Solution 0.1 mL
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2-8 °C
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1 each (1 each)
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≤-70 °C
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1 vial (20 μL)
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2-8 °C
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1 vial (75 μL)
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Akt Plate
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2-8 °C
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1 each (1 each)
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2-8 °C
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1 bottle (50 mL)
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2-8 °C
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1 bottle (200 mL)
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RT
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1 bottle (50 mL)
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RT
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1 bottle (15 g)
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Product Description
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Storage
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Quantity per Kit
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Phosphatase Inhibitor I 0.5mL
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2-8 °C
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1 each (1 each)
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Phosphatase Inhibitor II 0.5mL
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2-8 °C
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1 each (1 each)
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Protease Inhibitor Solution 0.5mL
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2-8 °C
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1 each (1 each)
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≤-70 °C
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5 vial (20 μL)
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2-8 °C
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1 vial (375 μL)
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Akt Plate
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2-8 °C
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5 each (1 each)
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2-8 °C
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1 bottle (50 mL)
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2-8 °C
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1 bottle (200 mL)
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RT
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1 bottle (50 mL)
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RT
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1 bottle (15 g)
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Product Description
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Storage
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Quantity per Kit
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Phosphatase Inhibitor I 0.5mL
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2-8 °C
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5 each (1 each)
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Phosphatase Inhibitor II 0.5mL
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2-8 °C
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5 each (1 each)
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Protease Inhibitor Solution 0.5mL
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2-8 °C
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5 each (1 each)
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≤-70 °C
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25 vial (20 μL)
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2-8 °C
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5 vial (375 μL)
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Akt Plate
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2-8 °C
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25 each (1 each)
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2-8 °C
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5 bottle (50 mL)
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2-8 °C
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5 bottle (200 mL)
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RT
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5 bottle (50 mL)
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RT
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5 bottle (15 g)
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Product Inserts
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Product Highlights
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Certificate of analysis
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SDS
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Title
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Journal
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Year
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Discovery of diverse and functional antibodies from large human repertoire antibody libraries.
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Dual blockade of the PI3K/AKT/mTOR (AZD8055) and RAS/MEK/ERK (AZD6244) pathways synergistically inhibits rhabdomyosarcoma cell growth in vitro and in vivo.
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Functional Consequences of the Macrophage Stimulating Protein 689C Inflammatory Bowel Disease Risk Allele.
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Multimodal microvascular imaging reveals that selective inhibition of class I PI3K is sufficient to induce an antivascular response.
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S49076 is a novel kinase inhibitor of MET, AXL and FGFR with strong preclinical activity alone and in association with bevacizumab.
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