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p akt2  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc p akt2
    P Akt2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 187 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+akt2/Phospho-Akt2+(Ser474)+Rabbit+mAb/pm41714926-106-23-26
    Average 95 stars, based on 187 article reviews
    p akt2 - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: Oxidized Low-Density Lipoprotein Accumulation in Macrophages Impairs Lipopolysaccharide-Induced Activation of AKT2, ATP Citrate Lyase, Acetyl-Coenzyme A Production, and Inflammatory Gene H3K27 Acetylation.
    Article Snippet: Membranes were blocked with 5% skim milk nonfat powder or 3% BSA (BioShop, no. ALB003) in TBST for 1 h at room temperature. .. Membranes were incubated with primary Abs overnight as follows: antiactin (Sigma-Aldrich, no. A2066), anti p-AKT (Ser473) (CST, no. 4060), anti p-AKT (Thr308) (CST, no. 4056), AKT (CST, no. 4685), anti p-PRAS40 (Thr246) (CST, no. 13175), anti-PRAS40 (CST, no. 2691), anti p-S6K (Thr389) (CST, no. 9234), anti-S6K (CST, no. 9202), anti p-S6 (Ser235/236) (CST, no. 4858), anti-S6 (CST, no. 2217), anti p-4EBP1 (Ser65) (CST, no. 9451), anti-4EBP1 (CST, no. 9644), anti p-GSK3a/b (Ser21/9) (CST, no. 9327), anti p-GSK3a/b (CST, no. 5676), anti p-AKT1 (Ser473) (CST, no. 9018), anti-AKT1 (CST, no. 2938), anti p-AKT2 (Ser474) (CST, no. 8599), anti-AKT2 (CST, no. 2964), anti p-AKT3 (Ser472) (Biorbyt, no. orb6790), anti-AKT3 (CST, no. 3788), anti p-ACLY (Ser455) (CST, no. 4331), anti-ACLY (Abcam, no. ab40793), anti p-TBK1 (Thr172) (CST, no. 5483), anti-TBK1 (CST, no. 38066), anti p-p65 (Ser536) (CST, no. 3033), anti-p65 (CST, no. 8242), anti p-ERK(Thr202/Tyr204) (CST, no. 4370), and anti-ERK (CST, no. 4695), followed by washing and incubation with HRP-conjugated anti-rabbit IgG (CST, no. 7074) (22 C, 1 h). .. Blots were developed using Immobilon Forte Western HRP substrate (Sigma-Aldrich, no. WBLUF0100), imaged with MicroChemi 4.2 (Bio-Rad), and analyzed with ImageJ.

    Article Title: LRRC8 complexes are adenosine nucleotide release channels regulating platelet activation and arterial thrombosis
    Article Snippet: Gels were transferred onto Immun-Blot PVDF Membranes (#1620177, Bio-Rad) in tris/glycine buffer (#1610771, Bio-Rad) for at 100 V for 1.5 h at 4°C. .. Membranes were then blocked in 5% bovine serum albumin (#A-420-10, GoldBio, St. Louis, MO, USA), or milk, in tris-buffered saline with Tween (TBS-T; 0.2 M Tris, 1.37 M NaCl, 0.2% Tween-20, pH 7.4) at room temperature for 1 h. Membranes were subsequently incubated with rabbit polyclonal anti-LRRC8A against the epitope QRTKSRIEQGIVDRSE (Pacific Immunology, Ramona, CA, USA), anti-LRRC8B*, anti-LRRC8C (#21601-1-AP, Proteintech, Rosemont, IL, USA), anti-LRRC8D*, anti-LRRC8E*, anti-AKT1 (#2938, Cell Signaling Technology, Danvers, MA, USA), anti-pAKT1 Ser473 (#9018, Cell Signaling Technology), anti-AKT2 (#3063, Cell Signaling Technology), anti-pAKT2 Ser474 (#8599, Cell Signaling Technology), anti-P-selectin (#AF737, R&D Systems, Minneapolis, MN, USA), anti-GSK-3β (#12456, Cell Signaling Technology), anti-pGSK-3β Ser9 (#9323, Cell Signaling Technology), anti-Integrin β3 (#sc-6627, Santa Cruz Biotechnology, Dallas, TX, USA), Anti-pPI3K p85 Tyr458 / p55 Tyr199 (#4228, Cell Signaling Technology), anti-β-Actin (#8457, Cell Signaling Technology), or anti-GAPDH (#5174, Cell Signaling Technology) at a concentration of 1:1000 in 1% BSA or milk overnight at 4°C (* Indicates antibodies which were kindly provided by T.J. Jentsch, previously validated in KO cell lines 75 ). .. Membranes were washed three times in TBS-T prior to incubation with goat anti-rabbit IgG (H+L)-Horseradish Peroxidase Conjugate (#1706515, Bio-Rad) or donkey anti-Goat IgG (H+L)-Horseradish Peroxidase Conjugate (Invitrogen #A15999, Thermo Fisher Scientific, Waltham, MA, USA) at a concentration of 1:5000 in 1% BSA or milk at room temperature for 1 h prior to further washing.

    Saline:

    Article Title: LRRC8 complexes are adenosine nucleotide release channels regulating platelet activation and arterial thrombosis
    Article Snippet: Gels were transferred onto Immun-Blot PVDF Membranes (#1620177, Bio-Rad) in tris/glycine buffer (#1610771, Bio-Rad) for at 100 V for 1.5 h at 4°C. .. Membranes were then blocked in 5% bovine serum albumin (#A-420-10, GoldBio, St. Louis, MO, USA), or milk, in tris-buffered saline with Tween (TBS-T; 0.2 M Tris, 1.37 M NaCl, 0.2% Tween-20, pH 7.4) at room temperature for 1 h. Membranes were subsequently incubated with rabbit polyclonal anti-LRRC8A against the epitope QRTKSRIEQGIVDRSE (Pacific Immunology, Ramona, CA, USA), anti-LRRC8B*, anti-LRRC8C (#21601-1-AP, Proteintech, Rosemont, IL, USA), anti-LRRC8D*, anti-LRRC8E*, anti-AKT1 (#2938, Cell Signaling Technology, Danvers, MA, USA), anti-pAKT1 Ser473 (#9018, Cell Signaling Technology), anti-AKT2 (#3063, Cell Signaling Technology), anti-pAKT2 Ser474 (#8599, Cell Signaling Technology), anti-P-selectin (#AF737, R&D Systems, Minneapolis, MN, USA), anti-GSK-3β (#12456, Cell Signaling Technology), anti-pGSK-3β Ser9 (#9323, Cell Signaling Technology), anti-Integrin β3 (#sc-6627, Santa Cruz Biotechnology, Dallas, TX, USA), Anti-pPI3K p85 Tyr458 / p55 Tyr199 (#4228, Cell Signaling Technology), anti-β-Actin (#8457, Cell Signaling Technology), or anti-GAPDH (#5174, Cell Signaling Technology) at a concentration of 1:1000 in 1% BSA or milk overnight at 4°C (* Indicates antibodies which were kindly provided by T.J. Jentsch, previously validated in KO cell lines 75 ). .. Membranes were washed three times in TBS-T prior to incubation with goat anti-rabbit IgG (H+L)-Horseradish Peroxidase Conjugate (#1706515, Bio-Rad) or donkey anti-Goat IgG (H+L)-Horseradish Peroxidase Conjugate (Invitrogen #A15999, Thermo Fisher Scientific, Waltham, MA, USA) at a concentration of 1:5000 in 1% BSA or milk at room temperature for 1 h prior to further washing.

    Concentration Assay:

    Article Title: LRRC8 complexes are adenosine nucleotide release channels regulating platelet activation and arterial thrombosis
    Article Snippet: Gels were transferred onto Immun-Blot PVDF Membranes (#1620177, Bio-Rad) in tris/glycine buffer (#1610771, Bio-Rad) for at 100 V for 1.5 h at 4°C. .. Membranes were then blocked in 5% bovine serum albumin (#A-420-10, GoldBio, St. Louis, MO, USA), or milk, in tris-buffered saline with Tween (TBS-T; 0.2 M Tris, 1.37 M NaCl, 0.2% Tween-20, pH 7.4) at room temperature for 1 h. Membranes were subsequently incubated with rabbit polyclonal anti-LRRC8A against the epitope QRTKSRIEQGIVDRSE (Pacific Immunology, Ramona, CA, USA), anti-LRRC8B*, anti-LRRC8C (#21601-1-AP, Proteintech, Rosemont, IL, USA), anti-LRRC8D*, anti-LRRC8E*, anti-AKT1 (#2938, Cell Signaling Technology, Danvers, MA, USA), anti-pAKT1 Ser473 (#9018, Cell Signaling Technology), anti-AKT2 (#3063, Cell Signaling Technology), anti-pAKT2 Ser474 (#8599, Cell Signaling Technology), anti-P-selectin (#AF737, R&D Systems, Minneapolis, MN, USA), anti-GSK-3β (#12456, Cell Signaling Technology), anti-pGSK-3β Ser9 (#9323, Cell Signaling Technology), anti-Integrin β3 (#sc-6627, Santa Cruz Biotechnology, Dallas, TX, USA), Anti-pPI3K p85 Tyr458 / p55 Tyr199 (#4228, Cell Signaling Technology), anti-β-Actin (#8457, Cell Signaling Technology), or anti-GAPDH (#5174, Cell Signaling Technology) at a concentration of 1:1000 in 1% BSA or milk overnight at 4°C (* Indicates antibodies which were kindly provided by T.J. Jentsch, previously validated in KO cell lines 75 ). .. Membranes were washed three times in TBS-T prior to incubation with goat anti-rabbit IgG (H+L)-Horseradish Peroxidase Conjugate (#1706515, Bio-Rad) or donkey anti-Goat IgG (H+L)-Horseradish Peroxidase Conjugate (Invitrogen #A15999, Thermo Fisher Scientific, Waltham, MA, USA) at a concentration of 1:5000 in 1% BSA or milk at room temperature for 1 h prior to further washing.

    other:

    Article Title: Phosphorylation of plectin by Akt3 promotes triple-negative breast cancer cell invasive migration
    Article Snippet: Anti-phospho-Akt substrate (pAkt-motif) (9614S), anti-phospho-Akt Ser473 (4060L), anti-Akt (4691S), anti-phospho-PRAS40 Thr246 (2997S), anti-PRAS40 (2691S), anti-phospho-GSK3β (9336S), anti-GSK3β (9315), anti-Akt1 (2938S), anti-Akt2 (3063S), anti-Akt3 (8018S), and anti-actin (3700S) were purchased from Cell Signaling Technology.

    Article Title: Pleiotropic tumor suppressive functions of PTEN missense mutations during gliomagenesis
    Article Snippet: anti-AKT2 , Cell Signaling Technology , 3063.



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    (A) Schematic overview of the canonical signaling events modulating muscle insulin action and its interaction with mTORC1 signaling. (B to D) Canonical insulin signaling as determined by phosphorylation of <t>Akt2</t> on Ser473 and Thr308, and phosphorylation of the Akt substrates GSK3β on Ser9 and TBC1D4 on Thr 642 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the hyperinsulinemic-euglycemic (HE) clamp. Levels of total Akt2, GSK3β, and TBC1D4 were comparable across groups and unaffected by insulin. (E and F) mTORC1 signaling as determined by phosphorylation of p70 S6 kinase (p70S6K) on Thr389 and S6 on Ser235/236 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the HE clamp. Levels of total p70S6K and S6 were comparable across groups and unaffected by insulin. Linear mixed models were used to estimate within– and between-group differences. Data are presented as observed individual values (with lines connecting individually matched participants) and estimated means ± 95% confidence limits, unless otherwise stated. For m.3243A>G carriers, individual datapoints are color-shaded to indicate muscle mtDNA heteroplasmy (light red = low, dark red = high). *Different from Basal ( P < 0.05). Basal, n = 30; Insulin, n = 27 (13 in m.3243A>G, 14 in Controls). Illustrations in (A) were created with BioRender.com.
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    Image Search Results


    (A) Schematic overview of the canonical signaling events modulating muscle insulin action and its interaction with mTORC1 signaling. (B to D) Canonical insulin signaling as determined by phosphorylation of Akt2 on Ser473 and Thr308, and phosphorylation of the Akt substrates GSK3β on Ser9 and TBC1D4 on Thr 642 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the hyperinsulinemic-euglycemic (HE) clamp. Levels of total Akt2, GSK3β, and TBC1D4 were comparable across groups and unaffected by insulin. (E and F) mTORC1 signaling as determined by phosphorylation of p70 S6 kinase (p70S6K) on Thr389 and S6 on Ser235/236 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the HE clamp. Levels of total p70S6K and S6 were comparable across groups and unaffected by insulin. Linear mixed models were used to estimate within– and between-group differences. Data are presented as observed individual values (with lines connecting individually matched participants) and estimated means ± 95% confidence limits, unless otherwise stated. For m.3243A>G carriers, individual datapoints are color-shaded to indicate muscle mtDNA heteroplasmy (light red = low, dark red = high). *Different from Basal ( P < 0.05). Basal, n = 30; Insulin, n = 27 (13 in m.3243A>G, 14 in Controls). Illustrations in (A) were created with BioRender.com.

    Journal: medRxiv

    Article Title: Physiological and molecular characterization of individuals carrying a diabetogenic mtDNA mutation establishes a mitochondrial basis for insulin resistance in humans

    doi: 10.64898/2025.12.17.25342274

    Figure Lengend Snippet: (A) Schematic overview of the canonical signaling events modulating muscle insulin action and its interaction with mTORC1 signaling. (B to D) Canonical insulin signaling as determined by phosphorylation of Akt2 on Ser473 and Thr308, and phosphorylation of the Akt substrates GSK3β on Ser9 and TBC1D4 on Thr 642 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the hyperinsulinemic-euglycemic (HE) clamp. Levels of total Akt2, GSK3β, and TBC1D4 were comparable across groups and unaffected by insulin. (E and F) mTORC1 signaling as determined by phosphorylation of p70 S6 kinase (p70S6K) on Thr389 and S6 on Ser235/236 in whole-muscle lysates from skeletal muscle biopsy samples obtained before (Basal) and immediately after (Insulin) the HE clamp. Levels of total p70S6K and S6 were comparable across groups and unaffected by insulin. Linear mixed models were used to estimate within– and between-group differences. Data are presented as observed individual values (with lines connecting individually matched participants) and estimated means ± 95% confidence limits, unless otherwise stated. For m.3243A>G carriers, individual datapoints are color-shaded to indicate muscle mtDNA heteroplasmy (light red = low, dark red = high). *Different from Basal ( P < 0.05). Basal, n = 30; Insulin, n = 27 (13 in m.3243A>G, 14 in Controls). Illustrations in (A) were created with BioRender.com.

    Article Snippet: The following antibodies were used: Phospho-Akt (Thr308) (Cell Signaling, catalog no. 9275); Phospho-Akt (Ser473) (Cell Signaling, catalog no. 9271); Akt2 (Cell Signaling, catalog no. 3063); Phospho-GSK-3β (Ser9) (Cell Signaling, catalog no. 5558); GSK-3β (BD Transduction Laboratories, catalog no. 610202); Phospho-TBC1D4 (Thr642) (Cell Signaling, catalog no. 8881); TBC1D4 (Abcam, catalog no. ab189890); Phospho-p70S6K (Thr389) (Cell Signaling, catalog no. 9205); p70S6K (Cell Signaling, catalog no. 9202); Phospho-S6 (Ser235/236) (Cell Signaling, catalog no. 4858); S6 (Cell Signaling, catalog no. 2217); PRDX2 (Abcam, catalog no. ab109367); PRDX3 (Abcam, catalog no. ab73349).

    Techniques: Phospho-proteomics