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anti cd36  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti cd36
    Anti Cd36, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 89 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd36/CD36+Rabbit+mAb/pmc13625660-123-21-23
    Average 95 stars, based on 89 article reviews
    anti cd36 - by Bioz Stars, 2026-10
    95/100 stars

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    Article Title: Preventive Effects of an Opuntia stricta var. dillenii Extract on Lipid Metabolism in a High-Fat High-Fructose Diet-Induced Obesity Animal Model.
    Article Snippet: Primary antibodies anti-total HSL, -CD36, -ATGL, -pACC and -total ACC were obtained from Cell Signalling Technology (Danvers, MA, USA).

    Incubation:

    Article Title: Differential Effects of Opuntia ficus-indica and Opuntia stricta var. dillenii Extracts on Liver Steatosis in a Murine Dietary Model
    Article Snippet: Proteins were separated via electrophoresis on 4–15% SDS-polyacrylamide gels and subsequently transferred to polyvinylidene difluoride (PVDF) membranes (Merck, Darmstadt, Germany). .. Membranes were incubated with 4% BSA for 1.5 h at room temperature, followed by overnight incubation at 4 °C with primary antibodies (1:1000) against FATP2 (Santa Cruz Biotech, Dallas, TX, USA), FATP5 (Lifespan Bioscience, Lynnwood, DC, USA), CD36 (Cell Signaling Danvers, MA, USA), AQP9 (Santa Cruz Biotech, Dallas, TX, USA), ChREBP (Novus Biologicals, Centennial, CO, USA), SREBP-1c (Abcam, Cambridge, UK), pACC (1Cell Signaling Danvers, MA, USA), ACC (Cell Signaling Danvers, MA, USA), FAS (Abcam, Cambridge, UK), pSIK1 (Thermo Fisher Scientific Inc., Rockford, IL, USA), SIK1 (Novus Biologicals, Centennial, CO, USA), DGAT2 (Abcam, Cambridge, UK), pAMPK (Cell Signaling Danvers, MA, USA), AMPK (Cell Signaling Danvers, MA, USA), SIRT1 (Abcam, Cambridge, UK), acetylated lysine (Cell Signaling Danvers, MA, USA), PGC-1α (1Novus Biologicals, Centennial, CO, USA), NRF1 (Abcam, Cambridge, UK), TFAM (Santa Cruz Biotech, Dallas, TX, USA), CPT1A (Abcam, Cambridge, UK), UCP2 (Santa Cruz Biotech, Dallas, TX, USA), ABHD5 (Invitrogen, Waltham, MA, USA), ATGL (Cell Signaling Danvers, MA, USA), MTP (Abcam, Cambridge, UK), pULK1 (Ser 757; Cell Signaling Danvers, MA, USA), ULK1 (Abcam, Cambridge, UK), LC3 (Cell Signaling Danvers, MA, USA), p62 (Abcam, Cambridge, UK), GAPDH (Abcam, Cambridge, UK), and histone H3 (Abcam, Cambridge, UK). .. Afterwards, membranes were incubated for 2 h at room temperature with the corresponding secondary antibodies (1:5000): polyclonal anti-mouse for AQP9, CPT1A, UCP2, p62, and GAPDH; anti-rabbit for FATP5, CD36, ChREBP, SREBP-1c, pACC, ACC, FAS, pSIK1, SIK1, DGAT2, pAMPK, AMPK, SIRT1, acetylated lysine, PGC-1α, NRF1, ABHD5, ATGL, MTP, pULK1, ULK1, LC3, and histone H3; and anti-goat for FATP2 and TFAM (all from Santa Cruz Biotech, Dallas, TX, USA).

    Article Title: Differential Effects of Opuntia ficus-indica and Opuntia stricta var. dillenii Extracts on Liver Steatosis in a Murine Dietary Model.
    Article Snippet: Proteins were separated via electrophoresis on 4–15% SDS-polyacrylamide gels and subsequently transferred to polyvinylidene difluoride (PVDF) membranes (Merck, Darmstadt, Germany). .. Membranes were incubated with 4% BSA for 1.5 h at room temperature, followed by overnight incubation at 4 ◦C with primary antibodies (1:1000) against FATP2 (Santa Cruz Biotech, Dallas, TX, USA), FATP5 (Lifespan Bioscience, Lynnwood, DC, USA), CD36 (Cell Signaling Danvers, MA, USA), AQP9 (Santa Cruz Biotech, Dallas, TX, USA), ChREBP (Novus Biologicals, Centennial, CO, USA), SREBP-1c (Abcam, Cambridge, UK), pACC (1Cell Signaling Danvers, MA, https://doi.org/10.3390/nu18030420 USA), ACC (Cell Signaling Danvers, MA, USA), FAS (Abcam, Cambridge, UK), pSIK1 (Thermo Fisher Scientific Inc., Rockford, IL, USA), SIK1 (Novus Biologicals, Centennial, CO, USA), DGAT2 (Abcam, Cambridge, UK), pAMPK (Cell Signaling Danvers, MA, USA), AMPK (Cell Signaling Danvers, MA, USA), SIRT1 (Abcam, Cambridge, UK), acetylated lysine (Cell Signaling Danvers, MA, USA), PGC-1α (1Novus Biologicals, Centennial, CO, USA), NRF1 (Abcam, Cambridge, UK), TFAM (Santa Cruz Biotech, Dallas, TX, USA), CPT1A (Abcam, Cambridge, UK), UCP2 (Santa Cruz Biotech, Dallas, TX, USA), ABHD5 (Invitrogen, Waltham, MA, USA), ATGL (Cell Signaling Danvers, MA, USA), MTP (Abcam, Cambridge, UK), pULK1 (Ser 757; Cell Signaling Danvers, MA, USA), ULK1 (Abcam, Cambridge, UK), LC3 (Cell Signaling Danvers, MA, USA), p62 (Abcam, Cambridge, UK), GAPDH (Abcam, Cambridge, UK), and histone H3 (Abcam, Cambridge, UK). .. Afterwards, membranes were incubated for 2 h at room temperature with the corresponding secondary antibodies (1:5000): polyclonal anti-mouse for AQP9, CPT1A, UCP2, p62, and GAPDH; anti-rabbit for FATP5, CD36, ChREBP, SREBP-1c, pACC, ACC, FAS, pSIK1, SIK1, DGAT2, pAMPK, AMPK, SIRT1, acetylated lysine, PGC-1α, NRF1, ABHD5, ATGL, MTP, pULK1, ULK1, LC3, and histone H3; and anti-goat for FATP2 and TFAM (all from Santa Cruz Biotech, Dallas, TX, USA).

    Article Title: Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance
    Article Snippet: Proteins were separated by SDS-PAGE and transferred to 0.45 μm polyvinyl difluoride (PVDF) membranes (Millipore) according to standard immunoblotting protocols. .. After blocking with 5% of defatted milk in TBST (20 mM of Tris-HCl pH 7.4, 500 mM of NaCl and 0.1% of Tween-20) for 1 h at room temperature, the membranes were incubated with the following primary antibodies: CD36 (#14347, 1:1000), Caspase 9 (#9502, 1:1000), Cytochrome-C (#4272, 1:1000), YAP (#14074, 1:1000), p-YAP (Ser127) (#4911, 1:1000) from Cell Signaling Technology; Cox-IV (ab14744, 1:5000), Histone H3 (ab1791, 1:5000), β-tublin (ab179513, 1:5000), CTGF (ab6992, 1:1000) from Abcam; Bcl-2 (sc-7382, 1:1000), Bak (sc-832, 1:1000), Bax (sc-6236, 1:1000) from Santa Cruz; Bim (AF1573, 1:1000) from Beyotime; Bid (MB0118, 1:1000) from bioworld; β-actin (A5441, 1:5000) from Sigma-Aldrich (St. Louis, USA); Ubiquitin Rabbit mAb (A19686, 1:1000) from ABclonal; Lamin B1 Ab (AB0054, 1:5000) from Abways. .. HRP-conjugated anti-rabbit IgG (Cell Signaling Tech, #7074) and anti-mouse IgG (Sigma-Aldrich, AP308P) were used as secondary antibodies.

    Article Title: Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance.
    Article Snippet: Proteins were separated by SDS-PAGE and transferred to 0.45 μm polyvinyl difluoride (PVDF) membranes (Millipore) according to standard immunoblotting protocols. .. After blocking with 5% of defatted milk in TBST (20 mM of Tris-HCl pH 7.4, 500 mM of NaCl and 0.1% of Tween-20) for 1 hr at room temperature, the membranes were incubated with the following primary antibodies: CD36 (#14347, 1:1000), Caspase 9 (#9502, 1:1000), Cytochrome-C (#4272, 1:1000), YAP (#14074, 1:1000), p-YAP (Ser127) (#4911, 1:1000) from Cell Signaling Technology; Cox-IV (ab14744, 1:5000), Histone H3 (ab1791, 1:5000), β-tublin (ab179513, 1:5000), CTGF (ab6992, 1:1000) from Abcam; Bcl-2 (sc-7382, 1:1000), Bak (sc-832, 1:1000), Bax (sc-6236, 1:1000) from Santa Cruz; Bim (AF1573, 1:1000) from Beyotime; Bid (MB0118, 1:1000) from bioworld; β-actin (A5441, 1:5000) from Sigma-Aldrich (St. Louis, USA);Ubiquitin Rabbit mAb (A19686, 1:1000) from ABclonal; Lamin B1 Ab (AB0054, 1:5000) from Abways. .. HRP-conjugated anti-rabbit IgG (Cell Signaling Tech, #7074) and anti-mouse IgG (Sigma-Aldrich, AP308P) were used as secondary antibodies.

    Pyrolysis Gas Chromatography:

    Article Title: Differential Effects of Opuntia ficus-indica and Opuntia stricta var. dillenii Extracts on Liver Steatosis in a Murine Dietary Model
    Article Snippet: Proteins were separated via electrophoresis on 4–15% SDS-polyacrylamide gels and subsequently transferred to polyvinylidene difluoride (PVDF) membranes (Merck, Darmstadt, Germany). .. Membranes were incubated with 4% BSA for 1.5 h at room temperature, followed by overnight incubation at 4 °C with primary antibodies (1:1000) against FATP2 (Santa Cruz Biotech, Dallas, TX, USA), FATP5 (Lifespan Bioscience, Lynnwood, DC, USA), CD36 (Cell Signaling Danvers, MA, USA), AQP9 (Santa Cruz Biotech, Dallas, TX, USA), ChREBP (Novus Biologicals, Centennial, CO, USA), SREBP-1c (Abcam, Cambridge, UK), pACC (1Cell Signaling Danvers, MA, USA), ACC (Cell Signaling Danvers, MA, USA), FAS (Abcam, Cambridge, UK), pSIK1 (Thermo Fisher Scientific Inc., Rockford, IL, USA), SIK1 (Novus Biologicals, Centennial, CO, USA), DGAT2 (Abcam, Cambridge, UK), pAMPK (Cell Signaling Danvers, MA, USA), AMPK (Cell Signaling Danvers, MA, USA), SIRT1 (Abcam, Cambridge, UK), acetylated lysine (Cell Signaling Danvers, MA, USA), PGC-1α (1Novus Biologicals, Centennial, CO, USA), NRF1 (Abcam, Cambridge, UK), TFAM (Santa Cruz Biotech, Dallas, TX, USA), CPT1A (Abcam, Cambridge, UK), UCP2 (Santa Cruz Biotech, Dallas, TX, USA), ABHD5 (Invitrogen, Waltham, MA, USA), ATGL (Cell Signaling Danvers, MA, USA), MTP (Abcam, Cambridge, UK), pULK1 (Ser 757; Cell Signaling Danvers, MA, USA), ULK1 (Abcam, Cambridge, UK), LC3 (Cell Signaling Danvers, MA, USA), p62 (Abcam, Cambridge, UK), GAPDH (Abcam, Cambridge, UK), and histone H3 (Abcam, Cambridge, UK). .. Afterwards, membranes were incubated for 2 h at room temperature with the corresponding secondary antibodies (1:5000): polyclonal anti-mouse for AQP9, CPT1A, UCP2, p62, and GAPDH; anti-rabbit for FATP5, CD36, ChREBP, SREBP-1c, pACC, ACC, FAS, pSIK1, SIK1, DGAT2, pAMPK, AMPK, SIRT1, acetylated lysine, PGC-1α, NRF1, ABHD5, ATGL, MTP, pULK1, ULK1, LC3, and histone H3; and anti-goat for FATP2 and TFAM (all from Santa Cruz Biotech, Dallas, TX, USA).

    Article Title: Differential Effects of Opuntia ficus-indica and Opuntia stricta var. dillenii Extracts on Liver Steatosis in a Murine Dietary Model.
    Article Snippet: Proteins were separated via electrophoresis on 4–15% SDS-polyacrylamide gels and subsequently transferred to polyvinylidene difluoride (PVDF) membranes (Merck, Darmstadt, Germany). .. Membranes were incubated with 4% BSA for 1.5 h at room temperature, followed by overnight incubation at 4 ◦C with primary antibodies (1:1000) against FATP2 (Santa Cruz Biotech, Dallas, TX, USA), FATP5 (Lifespan Bioscience, Lynnwood, DC, USA), CD36 (Cell Signaling Danvers, MA, USA), AQP9 (Santa Cruz Biotech, Dallas, TX, USA), ChREBP (Novus Biologicals, Centennial, CO, USA), SREBP-1c (Abcam, Cambridge, UK), pACC (1Cell Signaling Danvers, MA, https://doi.org/10.3390/nu18030420 USA), ACC (Cell Signaling Danvers, MA, USA), FAS (Abcam, Cambridge, UK), pSIK1 (Thermo Fisher Scientific Inc., Rockford, IL, USA), SIK1 (Novus Biologicals, Centennial, CO, USA), DGAT2 (Abcam, Cambridge, UK), pAMPK (Cell Signaling Danvers, MA, USA), AMPK (Cell Signaling Danvers, MA, USA), SIRT1 (Abcam, Cambridge, UK), acetylated lysine (Cell Signaling Danvers, MA, USA), PGC-1α (1Novus Biologicals, Centennial, CO, USA), NRF1 (Abcam, Cambridge, UK), TFAM (Santa Cruz Biotech, Dallas, TX, USA), CPT1A (Abcam, Cambridge, UK), UCP2 (Santa Cruz Biotech, Dallas, TX, USA), ABHD5 (Invitrogen, Waltham, MA, USA), ATGL (Cell Signaling Danvers, MA, USA), MTP (Abcam, Cambridge, UK), pULK1 (Ser 757; Cell Signaling Danvers, MA, USA), ULK1 (Abcam, Cambridge, UK), LC3 (Cell Signaling Danvers, MA, USA), p62 (Abcam, Cambridge, UK), GAPDH (Abcam, Cambridge, UK), and histone H3 (Abcam, Cambridge, UK). .. Afterwards, membranes were incubated for 2 h at room temperature with the corresponding secondary antibodies (1:5000): polyclonal anti-mouse for AQP9, CPT1A, UCP2, p62, and GAPDH; anti-rabbit for FATP5, CD36, ChREBP, SREBP-1c, pACC, ACC, FAS, pSIK1, SIK1, DGAT2, pAMPK, AMPK, SIRT1, acetylated lysine, PGC-1α, NRF1, ABHD5, ATGL, MTP, pULK1, ULK1, LC3, and histone H3; and anti-goat for FATP2 and TFAM (all from Santa Cruz Biotech, Dallas, TX, USA).

    Blocking Assay:

    Article Title: Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance
    Article Snippet: Proteins were separated by SDS-PAGE and transferred to 0.45 μm polyvinyl difluoride (PVDF) membranes (Millipore) according to standard immunoblotting protocols. .. After blocking with 5% of defatted milk in TBST (20 mM of Tris-HCl pH 7.4, 500 mM of NaCl and 0.1% of Tween-20) for 1 h at room temperature, the membranes were incubated with the following primary antibodies: CD36 (#14347, 1:1000), Caspase 9 (#9502, 1:1000), Cytochrome-C (#4272, 1:1000), YAP (#14074, 1:1000), p-YAP (Ser127) (#4911, 1:1000) from Cell Signaling Technology; Cox-IV (ab14744, 1:5000), Histone H3 (ab1791, 1:5000), β-tublin (ab179513, 1:5000), CTGF (ab6992, 1:1000) from Abcam; Bcl-2 (sc-7382, 1:1000), Bak (sc-832, 1:1000), Bax (sc-6236, 1:1000) from Santa Cruz; Bim (AF1573, 1:1000) from Beyotime; Bid (MB0118, 1:1000) from bioworld; β-actin (A5441, 1:5000) from Sigma-Aldrich (St. Louis, USA); Ubiquitin Rabbit mAb (A19686, 1:1000) from ABclonal; Lamin B1 Ab (AB0054, 1:5000) from Abways. .. HRP-conjugated anti-rabbit IgG (Cell Signaling Tech, #7074) and anti-mouse IgG (Sigma-Aldrich, AP308P) were used as secondary antibodies.

    Article Title: Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance.
    Article Snippet: Proteins were separated by SDS-PAGE and transferred to 0.45 μm polyvinyl difluoride (PVDF) membranes (Millipore) according to standard immunoblotting protocols. .. After blocking with 5% of defatted milk in TBST (20 mM of Tris-HCl pH 7.4, 500 mM of NaCl and 0.1% of Tween-20) for 1 hr at room temperature, the membranes were incubated with the following primary antibodies: CD36 (#14347, 1:1000), Caspase 9 (#9502, 1:1000), Cytochrome-C (#4272, 1:1000), YAP (#14074, 1:1000), p-YAP (Ser127) (#4911, 1:1000) from Cell Signaling Technology; Cox-IV (ab14744, 1:5000), Histone H3 (ab1791, 1:5000), β-tublin (ab179513, 1:5000), CTGF (ab6992, 1:1000) from Abcam; Bcl-2 (sc-7382, 1:1000), Bak (sc-832, 1:1000), Bax (sc-6236, 1:1000) from Santa Cruz; Bim (AF1573, 1:1000) from Beyotime; Bid (MB0118, 1:1000) from bioworld; β-actin (A5441, 1:5000) from Sigma-Aldrich (St. Louis, USA);Ubiquitin Rabbit mAb (A19686, 1:1000) from ABclonal; Lamin B1 Ab (AB0054, 1:5000) from Abways. .. HRP-conjugated anti-rabbit IgG (Cell Signaling Tech, #7074) and anti-mouse IgG (Sigma-Aldrich, AP308P) were used as secondary antibodies.

    Ubiquitin Proteomics:

    Article Title: Elevated CD36 drives lymph node metastasis of breast cancer by activating Hippo-YAP signaling-mediated anoikis resistance
    Article Snippet: Proteins were separated by SDS-PAGE and transferred to 0.45 μm polyvinyl difluoride (PVDF) membranes (Millipore) according to standard immunoblotting protocols. .. After blocking with 5% of defatted milk in TBST (20 mM of Tris-HCl pH 7.4, 500 mM of NaCl and 0.1% of Tween-20) for 1 h at room temperature, the membranes were incubated with the following primary antibodies: CD36 (#14347, 1:1000), Caspase 9 (#9502, 1:1000), Cytochrome-C (#4272, 1:1000), YAP (#14074, 1:1000), p-YAP (Ser127) (#4911, 1:1000) from Cell Signaling Technology; Cox-IV (ab14744, 1:5000), Histone H3 (ab1791, 1:5000), β-tublin (ab179513, 1:5000), CTGF (ab6992, 1:1000) from Abcam; Bcl-2 (sc-7382, 1:1000), Bak (sc-832, 1:1000), Bax (sc-6236, 1:1000) from Santa Cruz; Bim (AF1573, 1:1000) from Beyotime; Bid (MB0118, 1:1000) from bioworld; β-actin (A5441, 1:5000) from Sigma-Aldrich (St. Louis, USA); Ubiquitin Rabbit mAb (A19686, 1:1000) from ABclonal; Lamin B1 Ab (AB0054, 1:5000) from Abways. .. HRP-conjugated anti-rabbit IgG (Cell Signaling Tech, #7074) and anti-mouse IgG (Sigma-Aldrich, AP308P) were used as secondary antibodies.



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    Impact of high fat feeding and voluntary exercise on left ventricle morphology in male mice. (A) Representative images of Picrosirius red staining for measurement of interstitial and perivascular fibrosis with 20× magnification. (B) Representative images for Hematoxylin and Eosin for measurement of cardiomyocyte width and area with 40× magnification. (C) Representative images of Oil red O staining for measurement of interstitial lipid deposition with 40× magnification. Quantitative analysis of percent area of (D) interstitial and (E) perivascular fibrosis expressed as fold change from sedentary chow group. Quantitative analysis of (F) cardiomyocyte width and (G) cardiomyocyte area. (H) Quantitative analysis of percent area of lipid deposition expressed as fold change from sedentary chow group left ventricle mRNA expression of fatty acid transporters (I) FABP3, (J) <t>CD36,</t> and hypertrophy markers (K) β-MHC and (L) ANP in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (D–H) n : 8–12 per group. (I–L) n : 8–9 per group. * p < 0.05, **** p < 0.0001. ANP = atrial natriuretic peptide; β-MHC = beta myosin heavy chain; CD36 = platelet glycoprotein 4; FABP3 = fatty acid-binding protein 3; HFD = high fat diet; Myh7 = moysin heavy chain 7; VET = voluntary exercise training.
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    Impact of high fat feeding and voluntary exercise on left ventricle morphology in male mice. (A) Representative images of Picrosirius red staining for measurement of interstitial and perivascular fibrosis with 20× magnification. (B) Representative images for Hematoxylin and Eosin for measurement of cardiomyocyte width and area with 40× magnification. (C) Representative images of Oil red O staining for measurement of interstitial lipid deposition with 40× magnification. Quantitative analysis of percent area of (D) interstitial and (E) perivascular fibrosis expressed as fold change from sedentary chow group. Quantitative analysis of (F) cardiomyocyte width and (G) cardiomyocyte area. (H) Quantitative analysis of percent area of lipid deposition expressed as fold change from sedentary chow group left ventricle mRNA expression of fatty acid transporters (I) FABP3, (J) CD36, and hypertrophy markers (K) β-MHC and (L) ANP in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (D–H) n : 8–12 per group. (I–L) n : 8–9 per group. * p < 0.05, **** p < 0.0001. ANP = atrial natriuretic peptide; β-MHC = beta myosin heavy chain; CD36 = platelet glycoprotein 4; FABP3 = fatty acid-binding protein 3; HFD = high fat diet; Myh7 = moysin heavy chain 7; VET = voluntary exercise training.

    Journal: Journal of Sport and Health Science

    Article Title: Influence of diet-induced obesity and voluntary exercise training on cardiac lipids and mitochondrial function in mice

    doi: 10.1016/j.jshs.2025.101095

    Figure Lengend Snippet: Impact of high fat feeding and voluntary exercise on left ventricle morphology in male mice. (A) Representative images of Picrosirius red staining for measurement of interstitial and perivascular fibrosis with 20× magnification. (B) Representative images for Hematoxylin and Eosin for measurement of cardiomyocyte width and area with 40× magnification. (C) Representative images of Oil red O staining for measurement of interstitial lipid deposition with 40× magnification. Quantitative analysis of percent area of (D) interstitial and (E) perivascular fibrosis expressed as fold change from sedentary chow group. Quantitative analysis of (F) cardiomyocyte width and (G) cardiomyocyte area. (H) Quantitative analysis of percent area of lipid deposition expressed as fold change from sedentary chow group left ventricle mRNA expression of fatty acid transporters (I) FABP3, (J) CD36, and hypertrophy markers (K) β-MHC and (L) ANP in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Analysis was performed using two-way analysis of variance with Tukey’s post hoc test for multiple comparisons. Data are expressed as mean ± standard error of the mean. (D–H) n : 8–12 per group. (I–L) n : 8–9 per group. * p < 0.05, **** p < 0.0001. ANP = atrial natriuretic peptide; β-MHC = beta myosin heavy chain; CD36 = platelet glycoprotein 4; FABP3 = fatty acid-binding protein 3; HFD = high fat diet; Myh7 = moysin heavy chain 7; VET = voluntary exercise training.

    Article Snippet: The following TaqMan assay gene transcripts were used: fatty acid-binding protein 3 (FABP3, Mm02342495_m1), platelet glycoprotein 4 (CD36, Mm00432403_m1), beta myosin heavy chain (β-MHC, Mm00600555_m1), atrial natriuretic peptide (ANP, Mm01255747_g1), OPA1 (Mm01349707_g1), DRP1 (Mm01342903_m1), robosomal18S (18S, Mm03928990_g1).

    Techniques: Staining, Expressing, Binding Assay