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Genes | Free Full-Text | Reduced OPA1, Mitochondrial Fragmentation and Increased Susceptibility to Apoptosis in Granular Corneal Dystrophy Type 2 Corneal Fibroblasts
Genes | Free Full-Text | Reduced OPA1, Mitochondrial Fragmentation and Increased Susceptibility to Apoptosis in Granular Corneal Dystrophy Type 2 Corneal Fibroblasts

Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology - ScienceDirect
Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology - ScienceDirect

Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy | Molecular Neurodegeneration | Full Text
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy | Molecular Neurodegeneration | Full Text

OPA1 antibody (27733-1-AP) | Proteintech
OPA1 antibody (27733-1-AP) | Proteintech

Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell
Identification of new OPA1 cleavage site reveals that short isoforms regulate mitochondrial fusion | Molecular Biology of the Cell

Western blot analysis and quantitative analysis of OPA1 protein levels... | Download Scientific Diagram
Western blot analysis and quantitative analysis of OPA1 protein levels... | Download Scientific Diagram

OPA1 (D6U6N) Rabbit mAb | Cell Signaling Technology
OPA1 (D6U6N) Rabbit mAb | Cell Signaling Technology

OPA1 antibody (27733-1-AP) | Proteintech
OPA1 antibody (27733-1-AP) | Proteintech

OPA1 (D7C1A) Rabbit mAb | Cell Signaling Technology
OPA1 (D7C1A) Rabbit mAb | Cell Signaling Technology

OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion | PNAS
OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion | PNAS

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy - Caporali - 2020 - Annals of Neurology - Wiley Online Library
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy - Caporali - 2020 - Annals of Neurology - Wiley Online Library

OPA1 Antibody (D-9) | SCBT - Santa Cruz Biotechnology
OPA1 Antibody (D-9) | SCBT - Santa Cruz Biotechnology

Anti-OPA1 Antibody (A16345) | Antibodies.com
Anti-OPA1 Antibody (A16345) | Antibodies.com

HIGD‑1B inhibits hypoxia‑induced mitochondrial fragmentation by regulating OPA1 cleavage in cardiomyocytes
HIGD‑1B inhibits hypoxia‑induced mitochondrial fragmentation by regulating OPA1 cleavage in cardiomyocytes

Human OPA1 Antibody MAB9506-100: R&D Systems
Human OPA1 Antibody MAB9506-100: R&D Systems

OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L

OPA1 Polyclonal Antibody (PA5-57874)
OPA1 Polyclonal Antibody (PA5-57874)

OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific
OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific

Biomedicines | Free Full-Text | PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels
Biomedicines | Free Full-Text | PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels

OPA1 Antibody (1284B) - Azide and BSA Free (NBP2-80894): Novus Biologicals
OPA1 Antibody (1284B) - Azide and BSA Free (NBP2-80894): Novus Biologicals

OPA1 antibody (27733-1-AP) | Proteintech
OPA1 antibody (27733-1-AP) | Proteintech

Anti-OPA1 antibody [1E81D9] (ab119685) | Abcam
Anti-OPA1 antibody [1E81D9] (ab119685) | Abcam