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90
BeiGene Inc guangzhou biologics manufacturing co
Guangzhou Biologics Manufacturing Co, supplied by BeiGene Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Novus Biologicals pmpcb
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
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Cytiva Europe hitrap
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
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90
Valiant Co Ltd anti-gfp
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
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99
Enamine Ltd cetylpyridinium chloride
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Cetylpyridinium Chloride, supplied by Enamine Ltd, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytiva Europe pd-10 desalting column
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Pd 10 Desalting Column, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Techne corporation 4000-011-001
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
4000 011 001, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATS Scientific Inc hull lyostar 4.0 r&d/process development freeze dryer
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Hull Lyostar 4.0 R&D/Process Development Freeze Dryer, supplied by ATS Scientific 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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NSJ Bioreagents tag-72 antibody
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Tag 72 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytiva Europe sepharose 4b
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Sepharose 4b, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Shodex ohpak sb 805 hq
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
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JEOL jsm-7600f scanning electron microscope
Mitochondrial dynamic <t>and</t> <t>PMPCA</t> distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, <t>PMPCB,</t> OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.
Jsm 7600f Scanning Electron Microscope, supplied by JEOL, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Mitochondrial dynamic and PMPCA distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, PMPCB, OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.

Journal: Genes

Article Title: Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy

doi: 10.3390/genes13071202

Figure Lengend Snippet: Mitochondrial dynamic and PMPCA distribution studies of fibroblasts from control and PMPCA mutated patients. ( A ): Representative fluorescent images of mitochondrial network structure overlaid on phase-contrast (on the left) showed a mitochondrial network hyperconnection in PMPCA fibroblasts. Mitochondrial volume (in purple on black background in the middle) was assessed using the Mitotracker Green fluorescent signal by Imaris software and color-coded on the right. The inset illustrates the classification code. To present the changes in mitochondrial morphology in patients’ cells, types of mitochondria were classified into 5 groups according to mitochondrial length: blobs < 1 μm; fragmented < 5 μm; tubular < 10 μm; filamentous < 20 μm; mitochondrial network > 20 um. Bar graphs show the distribution of the mitochondrial population of Control, P1 and P2. Mean ± SEM. Scale bar: 10 μm. ( B ): Western blots (left) against PMPCA, PMPCB, OPA1 and citrate synthase (CS) on control (C1) and two patients’ (P1 and P2) fibroblasts reveal decreased levels of PMPCA and equal levels of PMPCB and OPA1 in the pathological conditions, as shown on the histogram (right). ( C ): Enzymatic activities of the respiratory complexes (CI to CV) from the control and the PMPCA mutated fibroblast strains related to the citrate synthase (CS) enzymatic activity, did not reveal a significant difference between control and mutated fibroblasts. Biochemical data were generated using the two-tailed paired t -test. Results are Mean ± S.E.M. from four independent experiments. ( D ): Single-molecule localization microscopy dSTORM was used to analyze PMPCA distribution, correlated to total internal reflection fluorescence TIRF microscopy for mitochondrial staining. Using Imaris 8.0 ® software, the dSTORM PMPCA immunofluorescence signal was used to quantify their mitochondrial surface protein distribution.

Article Snippet: Respiratory chain enzymatic activities and western blots were assessed as described [ , ], using the following antibodies: PMPCA (Novus Biologicals, CO, USA, #NBP1-89126; 56kD), PMPCB (Novus Biologicals, #NBP1-92120; 56kD); OPA1 (Abcam, Cambridge, England, ab42364; 95 and 85kD); Citrate Synthase (Abcam ab96600; 52kD).

Techniques: Control, Software, Western Blot, Activity Assay, Generated, Two Tailed Test, Microscopy, Fluorescence, Staining, Immunofluorescence