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mfn2 d2010  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc mfn2 d2010
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
Mfn2 D2010, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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d2010 plus microcentrifuge  (Dragon Laboratory)
86
Dragon Laboratory d2010 plus microcentrifuge
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
D2010 Plus Microcentrifuge, supplied by Dragon Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/d2010 plus microcentrifuge/product/Dragon Laboratory
Average 86 stars, based on 1 article reviews
d2010 plus microcentrifuge - by Bioz Stars, 2025-07
86/100 stars
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stabilat d2010  (FUJIFILM)
86
FUJIFILM stabilat d2010
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
Stabilat D2010, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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stabilat d2010 - by Bioz Stars, 2025-07
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d2010 spectrophotometer  (Danaher Inc)
86
Danaher Inc d2010 spectrophotometer
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
D2010 Spectrophotometer, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/d2010 spectrophotometer/product/Danaher Inc
Average 86 stars, based on 1 article reviews
d2010 spectrophotometer - by Bioz Stars, 2025-07
86/100 stars
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hach d2010 spectrophotometer  (Danaher Inc)
86
Danaher Inc hach d2010 spectrophotometer
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
Hach D2010 Spectrophotometer, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hach d2010 spectrophotometer/product/Danaher Inc
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hach d2010 spectrophotometer - by Bioz Stars, 2025-07
86/100 stars
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thermocirculator labtech d2010  (LabTech Inc)
86
LabTech Inc thermocirculator labtech d2010
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
Thermocirculator Labtech D2010, supplied by LabTech Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/thermocirculator labtech d2010/product/LabTech Inc
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thermocirculator labtech d2010 - by Bioz Stars, 2025-07
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wipo case no d2010 2011  (Mine Safety Appliances)
86
Mine Safety Appliances wipo case no d2010 2011
A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), <t>Mitofusin-2</t> <t>(MFN2)</t> and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.
Wipo Case No D2010 2011, supplied by Mine Safety Appliances, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/wipo case no d2010 2011/product/Mine Safety Appliances
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wipo case no d2010 2011 - by Bioz Stars, 2025-07
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d2010  (Santa Cruz Biotechnology)
86
Santa Cruz Biotechnology d2010
Antibodies for ChIP, western blot, immunocytochemistry, and immunohistochemistry. References, quantities and working dilutions are indicated. IF: immunofluorescence, WB: western blot, TMA: tissue microarray.
D2010, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/d2010/product/Santa Cruz Biotechnology
Average 86 stars, based on 1 article reviews
d2010 - by Bioz Stars, 2025-07
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söll d2010  (Biocell Technology)
86
Biocell Technology söll d2010
Antibodies for ChIP, western blot, immunocytochemistry, and immunohistochemistry. References, quantities and working dilutions are indicated. IF: immunofluorescence, WB: western blot, TMA: tissue microarray.
Söll D2010, supplied by Biocell Technology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/söll d2010/product/Biocell Technology
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Image Search Results


A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), Mitofusin-2 (MFN2) and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.

Journal: bioRxiv

Article Title: Cardiomyocyte STIM1 downregulation exacerbates post-Myocardial Infarction remodeling by dysregulating mitochondrial ultrastructure and metabolic signaling

doi: 10.1101/2024.12.05.625436

Figure Lengend Snippet: A. Transmission electron microscopy images from the left ventricles of Ctrl and shSTIM1 hearts 4 weeks post gene transfer showing differences in mitochondrial network ultrastructure and morphology. B . Mitochondrial dimensions (perimeters and areas) were quantified. C-D . Representative immunoblots and densitometric quantifications of total and phosphorylated DRP1 at Ser 637 and Ser 616 in tissue lysates from Ctrl and shSTIM1 hearts, 4 weeks post gene transfer. DRP1 protein levels were normalized to GAPDH and pDRP1 proteins were normalized to total DRP1 levels. shSTIM1 hearts showed a 55% and 21% increase in pS616/tDRP1 ratio (1.55±0.11 vs 1±0.09 in Ctrl) and p637/tDRP1 ratio (1.21±0.04 vs 1±0.03 in Ctrl), respectively versus Ctrl hearts. N=5 hearts per group was used. E-F . Representative immunoblots and densitometric quantifications of the major mitochondrial fission/fusion proteins, Mitofusin-1 (MFN1), Mitofusin-2 (MFN2) and OPA1 normalized to GAPDH in lysates from Ctrl and shSTIM1 hearts 4 weeks post gene transfer. While MFN1 and MFN2 protein levels were unchanged, OPA1 was decreased by 15.4% (84.6±2.4% vs 100±5.8% in Ctrl hearts). N=5 hearts per group. Statistics: t-test. GAPDH* and GAPDH# mean that the same GAPDH blot was used to normalize the expression of multiple proteins (as indicated in Panels C and E) after stripping the membrane and blotting for those proteins.

Article Snippet: Primary antibodies used were STIM1 (Sigma-Aldrich 6197), GAPDH (Cell Signaling 2118), DRP1 (Cell Signaling 8570), pDRP1-S616 (Cell Signaling 3455), pDRP1-S637 (Cell Signaling 4867), MFN1 (Proteintech 13798-1-AP), MFN2 (D2010) (Cell Signaling 9482), OPA1 (D6UN6) (Cell Signaling 80471), tAMPK (Cell Signaling 2532), pAMPK (Cell Signaling 2535), tACC (Cell Signaling 3661), pACC (Cell Signaling 3661), tRaptor (Cell Signaling 2280), pRaptor-S792 (Cell Signaling 2083), Cx43 (Cell Signaling 3512) and Nav1.5 (Alomone #ASC-005) were used.

Techniques: Transmission Assay, Electron Microscopy, Western Blot, Expressing, Stripping Membranes, Membrane

Antibodies for ChIP, western blot, immunocytochemistry, and immunohistochemistry. References, quantities and working dilutions are indicated. IF: immunofluorescence, WB: western blot, TMA: tissue microarray.

Journal: Cancers

Article Title: Global Decrease of Histone H3K27 Acetylation in ZEB1-Induced Epithelial to Mesenchymal Transition in Lung Cancer Cells

doi: 10.3390/cancers5020334

Figure Lengend Snippet: Antibodies for ChIP, western blot, immunocytochemistry, and immunohistochemistry. References, quantities and working dilutions are indicated. IF: immunofluorescence, WB: western blot, TMA: tissue microarray.

Article Snippet: Rabbit anti-ZEB1 , Santa Cruz Biotechnology, H102 , D2010 , 10 µg , 1:50 , , 1:50.

Techniques: Western Blot, Immunocytochemistry, Immunohistochemistry, Immunofluorescence, Microarray