OPA1 (D6U6N) Rabbit mAb | Cell Signaling Technology
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
Anti-OPA1 antibody (ab42364) | Abcam
OPA1‐dependent cristae modulation is essential for cellular adaptation to metabolic demand | The EMBO Journal
Western blot analysis and quantitative analysis of OPA1 protein levels... | Download Scientific Diagram
Genes | Free Full-Text | Reduced OPA1, Mitochondrial Fragmentation and Increased Susceptibility to Apoptosis in Granular Corneal Dystrophy Type 2 Corneal Fibroblasts
OPA1 (D7C1A) Rabbit mAb | Cell Signaling Technology
OPA1 (D6U6N) Rabbit mAb | Cell Signaling Technology
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L
OPA1 Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1B2D8, Proteintech 150 μL; Unconjugated Products | Fisher Scientific
Western blot analysis of OPA1. (A) Western blot analysis of OPA1... | Download Scientific Diagram
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions
Biomedicines | Free Full-Text | PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels
Western blot analysis and quantification of OPA1 protein expression (A)... | Download Scientific Diagram
OPA1 antibody (27733-1-AP) | Proteintech
Human OPA1 Antibody MAB9506-100: R&D Systems
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
Frontiers | OPA1-Exon4b Binds to mtDNA D-Loop for Transcriptional and Metabolic Modulation, Independent of Mitochondrial Fusion
p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to maintain mitochondrial connectivity related to mitochondrial dysfunction and apoptosis | Scientific Reports
Anti-OPA1 Antibody Picoband™ | Bosterbio
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy - Caporali - 2020 - Annals of Neurology - Wiley Online Library
OPA1 antibody (27733-1-AP) | Proteintech
