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65°c water bath  (Thermo Fisher)


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    Thermo Fisher 65°c water bath
    65°C Water Bath, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/%E2%97%A6+c/10__22175_slash_mmb__17751-107-11-13
    Average 90 stars, based on 1 article reviews
    65°c water bath - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Human Umbilical Cord Mesenchymal Stem Cell-Derived Extracellular Vesicles Loaded with Emodin Alleviate Intestinal Injury in Acute Pancreatitis.
    Article Snippet: The cell suspension was centrifuged at 1200 rpm for 3 min (Eppendorf, TSGP10). .. CCD-841CON cells were resuspended in DMEM/F12 medium supplemented with 10% foetal bovine serum (ExCell Bio, Cat. FCS500) and 1% penicillinstreptomycin (ThermoFisher, Cat. 15070063) in DMEM/F12 medium, and cultured in a 6 cm culture dish (Corning, 354401) at 37◦C under 5% CO2 (ThermoFisher, 3311E). hUC-MSCs were cultured in the vendor-supplied dedicatedmedium (IMMOCELL, Cat. IMP-H054-1). .. For subculture, confluent cells were washed with phosphate buffer solution (PBS, Corning, Cat. 21-040-CV), digested with 0.25% trypsin (IMMOCELL, Cat. IMC-305) at 37◦C until detachment, and neutralized with complete medium.

    Incubation:

    Article Title: Tumor-specific glyco-detonators: A neuraminidase-3-gated programmable DNA Nanoarchitectonics for liver cancer-exclusive chemotherapy.
    Article Snippet: The silent progression and lack of reliable biomarkers for early-stage hepatocellular carcinoma (HCC) often lead to late-stage diagnoses, where conventional chemotherapies are highly toxic and offer limited efficacy.. To bridge this diagnostic-therapeutic gap, we designed a DNA nanocomputer that functions as a biological logic gate, converting a pathological marker into a therapeutic command.. This “dual-lock” system uses sialic acid ‘caps’ to mask galactose ligands on a DNA scaffold.

    Article Title: Carbamate-based cannabinoids uncover a conserved lipid-sensing pocket in nociceptive TRPA1 and TRPV1 channels.
    Article Snippet: .. Briefly, transfected rTRPV1, rTRPV2, hTRPV1 or hTRPA1 HEK293T cells (wt or mutated); rTRPV1 or hTRPA1 Flp-In TREx 293 stable cells were spotted at Poly-D-Lysine (PDL, 0.1 mg/mL) coated imaging chambers (μ-slide, 8 well) and incubated for 30–40 min in a humidified incubator at 37◦C and 5% CO2 before being loaded with 5 μM Fura− 2 AM (Invitrogen; cat. no. F1201) dissolved in Ringer's solution (in mM: 140 NaCl, 2.5 KCl, 1.8 CaCl2, 2 MgSO4, 20 HEPES and 5 D-glucose, pH 7.4 with NaOH) supplemented with Pluronic F− 127 acid (Sigma-Aldrich; 0.01%) and incubated for 1 hr in the dark at RT. ..

    Article Title: De novo pyrimidine synthesis controls germinal center B cell and plasma cell fates and systemic autoimmunity.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER PerCP/Cy5.5 Conjugation Kit – Lightning Link AbCam Cat# ab102911 Alexa Fluor 647 Conjugation Kit (Fast) – Lightning Link AbCam Cat# ab269823 CellTrace Yellow Cell Proliferation kit, for flow cytometry Invitrogen Cat# C34573 Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit Thermo Fisher Scientific Cat# C10425 EasySep Mouse B cell Isolation Kit StemCell Technologies Cat# 19854 Seahorse XFe96/XF Pro FluxPak Agilent Technologies Cat# 103792-100 Immulon 4 HBX 96-well plates Thermo Scientific Cat# 3855 Multiscreen hydrophobic PVDF plates Millipore Sigma Cat# MSIPS4W10 Hep–2 slides Antibodies Incorporated Cat# 15-112 High-capacity cDNA Reverse Transcription Kit Thermo Fisher Scientific Cat# 4374966 ADP/ATP Ratio Assay Kit Sigma Aldrich Cat# MAK135 nCounter Mouse Metabolic Pathways Panel nanoString Technologies Cat# XT-CSO-MMP1-12 Deposited data RNA-sequencing Raw and processed data This paper GEO: GSE329002 Metabolomics and isotope tracing Raw data This paper Metabolomics Workbench: Project ID PR003059 https://doi.org/10.21228/M88G4 Experimental models: Organisms/strains Mouse: B6: C57BL/6 Jackson Laboratories Strain: 000664; RRID: IMSR_JAX:000664 Mouse: FcγRIIB− /− : B6;129 S-Fcgr2btm1Ttk/J Jackson Laboratories Strain: 002848; RRID: IMSR_JAX:002848 Mouse: B6.yaa: B6.SB-Yaa-J Jackson Laboratories Strain: 000483; RRID: IMSR_JAX:000483 Mouse: UMPSfl: C57BL/6 J-Umpsem1Cflox/Cya Cyagen Cat# S-CKO_06542; Strain ID: CKOCMP-22247- Umps-B6J-VA Mouse: CD23Cre+: B6.Cg-Tg(Fcer2a-cre)5Mbu Jackson Laboratories Strain: 028197; RRID: IMSR_JAX:028197 Software and algorithms FlowJo v9 and v10 Waters Biosciences http://www.flowjo.com Seahorse Wave Pro Agilent Technologies N/A Agilent Seahorse Analytics Agilent Technologies N/A Perseus Tyanova et al.63 N/A nSolver 4.0 Analysis Software nanoString Technologies N/A Leica Application Suite (LAS) X software Leica Microsystems N/A NovaSeq Control Software (NCS) Illumina N/A Illumina bcl2fastq Conversion Software v2.20 Illumina N/A GeneSCF Subhash and Kanduri64 N/A Panther Classification System Gene Ontology Paul Thomas Lab https://pantherdb.org Cell Reports 45, 117587, July 28, 2026 23 figure legend. .. B cells were incubated at 37◦C for 24 h, then 6-azauridine was added at the indicated concentrations and cells were incubated for another 72 h. To detect EdU by flow cytometry, cells were surface stained, then Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit was used according to manufacturer’s protocol (ThermoFisher Scientific). .. Stained cells were analyzed on a BD FACSymphony A5 Cell Analyzer (BD Biosciences).

    Article Title: Sex-specific acceleration of Alzheimer's pathogenesis by chronic sleep-deprivation.
    Article Snippet: .. Following three 5-min TBS-T washes, membranes were incubated overnight at 4◦C with primary antibodies described in Table S2 in SuperBlock/TBS solution: ATG5 (Invitrogen, Catalog No.: PA1-46178), Beclin-1 (Invitrogen, Catalog No.: 66665-1-Ig), GAPDH (Millipore Sigma, CatalogNo. .. : G8795), LC3B (Cell Signaling Technology, Catalog No.: 2775S), and PHF1 (Albert Einstein College of Medicine, Catalog No.: AB_2315150).

    Concentration Assay:

    Article Title: Tumor-specific glyco-detonators: A neuraminidase-3-gated programmable DNA Nanoarchitectonics for liver cancer-exclusive chemotherapy.
    Article Snippet: The silent progression and lack of reliable biomarkers for early-stage hepatocellular carcinoma (HCC) often lead to late-stage diagnoses, where conventional chemotherapies are highly toxic and offer limited efficacy.. To bridge this diagnostic-therapeutic gap, we designed a DNA nanocomputer that functions as a biological logic gate, converting a pathological marker into a therapeutic command.. This “dual-lock” system uses sialic acid ‘caps’ to mask galactose ligands on a DNA scaffold.

    Conjugation Assay:

    Article Title: Tumor-specific glyco-detonators: A neuraminidase-3-gated programmable DNA Nanoarchitectonics for liver cancer-exclusive chemotherapy.
    Article Snippet: The silent progression and lack of reliable biomarkers for early-stage hepatocellular carcinoma (HCC) often lead to late-stage diagnoses, where conventional chemotherapies are highly toxic and offer limited efficacy.. To bridge this diagnostic-therapeutic gap, we designed a DNA nanocomputer that functions as a biological logic gate, converting a pathological marker into a therapeutic command.. This “dual-lock” system uses sialic acid ‘caps’ to mask galactose ligands on a DNA scaffold.

    Liquid Chromatography with Mass Spectroscopy:

    Article Title: Tumor-specific glyco-detonators: A neuraminidase-3-gated programmable DNA Nanoarchitectonics for liver cancer-exclusive chemotherapy.
    Article Snippet: The silent progression and lack of reliable biomarkers for early-stage hepatocellular carcinoma (HCC) often lead to late-stage diagnoses, where conventional chemotherapies are highly toxic and offer limited efficacy.. To bridge this diagnostic-therapeutic gap, we designed a DNA nanocomputer that functions as a biological logic gate, converting a pathological marker into a therapeutic command.. This “dual-lock” system uses sialic acid ‘caps’ to mask galactose ligands on a DNA scaffold.

    Mass Spectrometry:

    Article Title: Tumor-specific glyco-detonators: A neuraminidase-3-gated programmable DNA Nanoarchitectonics for liver cancer-exclusive chemotherapy.
    Article Snippet: The silent progression and lack of reliable biomarkers for early-stage hepatocellular carcinoma (HCC) often lead to late-stage diagnoses, where conventional chemotherapies are highly toxic and offer limited efficacy.. To bridge this diagnostic-therapeutic gap, we designed a DNA nanocomputer that functions as a biological logic gate, converting a pathological marker into a therapeutic command.. This “dual-lock” system uses sialic acid ‘caps’ to mask galactose ligands on a DNA scaffold.

    Transfection:

    Article Title: Carbamate-based cannabinoids uncover a conserved lipid-sensing pocket in nociceptive TRPA1 and TRPV1 channels.
    Article Snippet: .. Briefly, transfected rTRPV1, rTRPV2, hTRPV1 or hTRPA1 HEK293T cells (wt or mutated); rTRPV1 or hTRPA1 Flp-In TREx 293 stable cells were spotted at Poly-D-Lysine (PDL, 0.1 mg/mL) coated imaging chambers (μ-slide, 8 well) and incubated for 30–40 min in a humidified incubator at 37◦C and 5% CO2 before being loaded with 5 μM Fura− 2 AM (Invitrogen; cat. no. F1201) dissolved in Ringer's solution (in mM: 140 NaCl, 2.5 KCl, 1.8 CaCl2, 2 MgSO4, 20 HEPES and 5 D-glucose, pH 7.4 with NaOH) supplemented with Pluronic F− 127 acid (Sigma-Aldrich; 0.01%) and incubated for 1 hr in the dark at RT. ..

    Imaging:

    Article Title: Carbamate-based cannabinoids uncover a conserved lipid-sensing pocket in nociceptive TRPA1 and TRPV1 channels.
    Article Snippet: .. Briefly, transfected rTRPV1, rTRPV2, hTRPV1 or hTRPA1 HEK293T cells (wt or mutated); rTRPV1 or hTRPA1 Flp-In TREx 293 stable cells were spotted at Poly-D-Lysine (PDL, 0.1 mg/mL) coated imaging chambers (μ-slide, 8 well) and incubated for 30–40 min in a humidified incubator at 37◦C and 5% CO2 before being loaded with 5 μM Fura− 2 AM (Invitrogen; cat. no. F1201) dissolved in Ringer's solution (in mM: 140 NaCl, 2.5 KCl, 1.8 CaCl2, 2 MgSO4, 20 HEPES and 5 D-glucose, pH 7.4 with NaOH) supplemented with Pluronic F− 127 acid (Sigma-Aldrich; 0.01%) and incubated for 1 hr in the dark at RT. ..

    Polymerase Chain Reaction:

    Article Title: Germline sequence variation within the ribosomal DNA is associated with human complex traits.
    Article Snippet: .. Preparation of LCL cell line lysate was adapted from a public protocol for polysome profiling followed by quantitative PCR.64 A minimum of 50 million LCLs were treated with 100μg/ml cycloheximide (Thermo Fisher Scientific Cat. No. J66004.XF) for 15 min at 37◦C. .. Cells were pelleted by centrifugation at 500g for 3 min at 4◦C, and washed twice with ice-cold PBS (Thermo Fisher Scientific Cat. No. 10010023) supplemented with 100μg/ml cycloheximide.

    Flow Cytometry:

    Article Title: De novo pyrimidine synthesis controls germinal center B cell and plasma cell fates and systemic autoimmunity.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER PerCP/Cy5.5 Conjugation Kit – Lightning Link AbCam Cat# ab102911 Alexa Fluor 647 Conjugation Kit (Fast) – Lightning Link AbCam Cat# ab269823 CellTrace Yellow Cell Proliferation kit, for flow cytometry Invitrogen Cat# C34573 Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit Thermo Fisher Scientific Cat# C10425 EasySep Mouse B cell Isolation Kit StemCell Technologies Cat# 19854 Seahorse XFe96/XF Pro FluxPak Agilent Technologies Cat# 103792-100 Immulon 4 HBX 96-well plates Thermo Scientific Cat# 3855 Multiscreen hydrophobic PVDF plates Millipore Sigma Cat# MSIPS4W10 Hep–2 slides Antibodies Incorporated Cat# 15-112 High-capacity cDNA Reverse Transcription Kit Thermo Fisher Scientific Cat# 4374966 ADP/ATP Ratio Assay Kit Sigma Aldrich Cat# MAK135 nCounter Mouse Metabolic Pathways Panel nanoString Technologies Cat# XT-CSO-MMP1-12 Deposited data RNA-sequencing Raw and processed data This paper GEO: GSE329002 Metabolomics and isotope tracing Raw data This paper Metabolomics Workbench: Project ID PR003059 https://doi.org/10.21228/M88G4 Experimental models: Organisms/strains Mouse: B6: C57BL/6 Jackson Laboratories Strain: 000664; RRID: IMSR_JAX:000664 Mouse: FcγRIIB− /− : B6;129 S-Fcgr2btm1Ttk/J Jackson Laboratories Strain: 002848; RRID: IMSR_JAX:002848 Mouse: B6.yaa: B6.SB-Yaa-J Jackson Laboratories Strain: 000483; RRID: IMSR_JAX:000483 Mouse: UMPSfl: C57BL/6 J-Umpsem1Cflox/Cya Cyagen Cat# S-CKO_06542; Strain ID: CKOCMP-22247- Umps-B6J-VA Mouse: CD23Cre+: B6.Cg-Tg(Fcer2a-cre)5Mbu Jackson Laboratories Strain: 028197; RRID: IMSR_JAX:028197 Software and algorithms FlowJo v9 and v10 Waters Biosciences http://www.flowjo.com Seahorse Wave Pro Agilent Technologies N/A Agilent Seahorse Analytics Agilent Technologies N/A Perseus Tyanova et al.63 N/A nSolver 4.0 Analysis Software nanoString Technologies N/A Leica Application Suite (LAS) X software Leica Microsystems N/A NovaSeq Control Software (NCS) Illumina N/A Illumina bcl2fastq Conversion Software v2.20 Illumina N/A GeneSCF Subhash and Kanduri64 N/A Panther Classification System Gene Ontology Paul Thomas Lab https://pantherdb.org Cell Reports 45, 117587, July 28, 2026 23 figure legend. .. B cells were incubated at 37◦C for 24 h, then 6-azauridine was added at the indicated concentrations and cells were incubated for another 72 h. To detect EdU by flow cytometry, cells were surface stained, then Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit was used according to manufacturer’s protocol (ThermoFisher Scientific). .. Stained cells were analyzed on a BD FACSymphony A5 Cell Analyzer (BD Biosciences).

    Staining:

    Article Title: De novo pyrimidine synthesis controls germinal center B cell and plasma cell fates and systemic autoimmunity.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER PerCP/Cy5.5 Conjugation Kit – Lightning Link AbCam Cat# ab102911 Alexa Fluor 647 Conjugation Kit (Fast) – Lightning Link AbCam Cat# ab269823 CellTrace Yellow Cell Proliferation kit, for flow cytometry Invitrogen Cat# C34573 Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit Thermo Fisher Scientific Cat# C10425 EasySep Mouse B cell Isolation Kit StemCell Technologies Cat# 19854 Seahorse XFe96/XF Pro FluxPak Agilent Technologies Cat# 103792-100 Immulon 4 HBX 96-well plates Thermo Scientific Cat# 3855 Multiscreen hydrophobic PVDF plates Millipore Sigma Cat# MSIPS4W10 Hep–2 slides Antibodies Incorporated Cat# 15-112 High-capacity cDNA Reverse Transcription Kit Thermo Fisher Scientific Cat# 4374966 ADP/ATP Ratio Assay Kit Sigma Aldrich Cat# MAK135 nCounter Mouse Metabolic Pathways Panel nanoString Technologies Cat# XT-CSO-MMP1-12 Deposited data RNA-sequencing Raw and processed data This paper GEO: GSE329002 Metabolomics and isotope tracing Raw data This paper Metabolomics Workbench: Project ID PR003059 https://doi.org/10.21228/M88G4 Experimental models: Organisms/strains Mouse: B6: C57BL/6 Jackson Laboratories Strain: 000664; RRID: IMSR_JAX:000664 Mouse: FcγRIIB− /− : B6;129 S-Fcgr2btm1Ttk/J Jackson Laboratories Strain: 002848; RRID: IMSR_JAX:002848 Mouse: B6.yaa: B6.SB-Yaa-J Jackson Laboratories Strain: 000483; RRID: IMSR_JAX:000483 Mouse: UMPSfl: C57BL/6 J-Umpsem1Cflox/Cya Cyagen Cat# S-CKO_06542; Strain ID: CKOCMP-22247- Umps-B6J-VA Mouse: CD23Cre+: B6.Cg-Tg(Fcer2a-cre)5Mbu Jackson Laboratories Strain: 028197; RRID: IMSR_JAX:028197 Software and algorithms FlowJo v9 and v10 Waters Biosciences http://www.flowjo.com Seahorse Wave Pro Agilent Technologies N/A Agilent Seahorse Analytics Agilent Technologies N/A Perseus Tyanova et al.63 N/A nSolver 4.0 Analysis Software nanoString Technologies N/A Leica Application Suite (LAS) X software Leica Microsystems N/A NovaSeq Control Software (NCS) Illumina N/A Illumina bcl2fastq Conversion Software v2.20 Illumina N/A GeneSCF Subhash and Kanduri64 N/A Panther Classification System Gene Ontology Paul Thomas Lab https://pantherdb.org Cell Reports 45, 117587, July 28, 2026 23 figure legend. .. B cells were incubated at 37◦C for 24 h, then 6-azauridine was added at the indicated concentrations and cells were incubated for another 72 h. To detect EdU by flow cytometry, cells were surface stained, then Click-iT EdU Alexa Fluor 488 Flow Cytometry Assay Kit was used according to manufacturer’s protocol (ThermoFisher Scientific). .. Stained cells were analyzed on a BD FACSymphony A5 Cell Analyzer (BD Biosciences).

    Article Title: Bioactive fibrous microwell platforms induce m1 macrophage clusters that enhance anti-tumor activity and T cell polarization
    Article Snippet: Engineering immune-regulatory microenvironments that direct macrophage function is central to advancing immunotherapies for solid tumors.. Here, we present a bioactive fibrous microwell platform that integrates electrospun polycaprolactone/polyvinylpyrrolidone (PCL/PVP) nanofibers with photopatterned threedimensional confinement and sustained lipopolysaccharide (LPS) delivery, enabling the formation of stable M1-polarized macrophage clusters beyond conventional transient stimulation.. The hybrid microenvironment guided macrophages into compact clusters while providing continuous pro-inflammatory cues.

    Suspension:

    Article Title: ZBTB21 Is a Dual Suppressor of Pyroptosis and MHC-I Antigen Presentation That Promotes Tumor Immune Evasion.
    Article Snippet: .. The tissue fragments were resuspended in 10 mL of Hank’s Solution containing 2 mg/mL collagenase I (Gibco, Cat#17100017) and digested at 37◦C with shaking at 140 rpm for 50 min. Digestion was terminated by adding an equal volume of complete medium, and the resulting cell suspension was filtered through a 40 μm cell strainer into a new 50 mL centrifuge tube. .. After centrifugation at 1800 rpm for 5 min, the supernatant was removed, and the pellet was resuspended in 1 mL of erythrocyte lysis buffer (Solarbio, Cat#R1010) for 10 min on ice to lyse red blood cells.



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    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = <t>cytochrome</t> <t>c</t> oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.
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    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.
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    PromoCell human umbilical vein endothelial cells (huvec) pooled
    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.
    Human Umbilical Vein Endothelial Cells (Huvec) Pooled, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/%E2%97%A6+c/Human+Umbilical+Vein+Endothelial+Cells+(HUVEC)+pooled/custom%40c-12203%4042668579
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    ATCC c hutchinsonii atcc 33406
    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.
    C Hutchinsonii Atcc 33406, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/%E2%97%A6+c/Cytophaga+hutchinsonii+Winogradsky/pmc12860637-1-0-2
    Average 95 stars, based on 1 article reviews
    c hutchinsonii atcc 33406 - by Bioz Stars, 2026-09
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    Image Search Results


    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; 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: Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Article Snippet: The plate was centrifuged at 500 g for 5 min at 4°C, and 140 μL of MAS buffer containing 10 μg/mL cytochrome C (Thermo Fisher Scientific) was pipetted to each well.

    Techniques: Expressing, Western Blot, Isolation, Marker, Control, Membrane

    Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; 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: Voluntary exercise alters left ventricle gene and protein expression related to mitochondrial biogenesis and dynamics in high fat- and chow-fed mice. (A) Western blot analysis to assess purity of crude mitochondria isolation where left ventricle mitochondrial pellet expresses mitochondrial marker TOM70 and COXIV and supernatant expresses calnexin. Protein expression of (B) LCLAT1 and (C) MFN2 in left ventricle-isolated crude mitochondria and (D) LCLAT1, (E) PGC-1α, and (F) MFN2 in left ventricle tissue from male VET or sedentary mice fed an HFD or chow diet. Left ventricle mRNA expression of (G) OPA1 and (H) DRP1 in male VET or sedentary mice fed an HFD or chow diet. Values were calculated relative to 18S housekeeper. Calnexin and β-actin were used as internal controls of protein loading in left ventricle samples and COXIV as internal control of protein loading in crude mitochondria samples. 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. (B–C) n : 5–6 per group. (D–F) n = 7 per group. (G and H) n = 9 per group. CE = chow exercise; CS = chow sedentary; COXIV = cytochrome c oxidase subunit 4; DRP1 = dynamin-related protein 1; HE = high fat diet exercise; HFD = high fat diet; HS = high fat diet sedentary; LCLAT1 = lysocardiolipin acyltransferase 1; MFN2 = mitofusin-2; OPA1 = optic atrophy 1; PGC-1α = peroxisome proliferator-activated receptor gamma coactivator-1α; TOM70 = translocase of outer mitochondria membrane 70; VET = voluntary exercise training.

    Article Snippet: Immunoblotting was performed with antibodies against lysocardiolipin acyltransferase 1(LCLAT1, PA5-25627; Thermo Fisher Scientific), PGC-1α (ab191838; Abcam, Cambridge, UK), MFN2 (PA5-118059; Thermo Fisher Scientific), ANP (sc-18811; Santa Cruz, Dallas, TX, USA), tumor necrosis factor alpha (TNFα, 3707; Cell Signaling, Danvers, MA, USA), phosphorylated adenosine monophosphate-activated protein kinase (AMPK, 2531; Cell Signaling), AMPKα (2532; Cell Signaling), Perilipin 5 (PA1-46215; Thermo Fisher Scientific), translocase of outer mitochondria membrane 70 (TOM70, 65675; Cell Signaling), cytochrome c oxidase subunit 4 (COXIV, 4844; Cell Signaling), and calnexin (208880; Merck, Rahway, NJ, USA).

    Techniques: Expressing, Western Blot, Isolation, Marker, Control, Membrane