Home

gebrochen alltäglich Waffenkammer opa1 western blot locker Kissen Elite

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

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

OPA1 antibody (66583-1-Ig) | Proteintech
OPA1 antibody (66583-1-Ig) | Proteintech

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

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

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

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

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

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

p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to  maintain mitochondrial connectivity related to mitochondrial dysfunction  and apoptosis | Scientific Reports
p32/C1QBP regulates OMA1-dependent proteolytic processing of OPA1 to maintain mitochondrial connectivity related to mitochondrial dysfunction and apoptosis | Scientific Reports

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

Anti-OPA1 Antibody Picoband™ | Bosterbio
Anti-OPA1 Antibody Picoband™ | Bosterbio

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

OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions
OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions

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‐dependent cristae modulation is essential for cellular adaptation to  metabolic demand | The EMBO Journal
OPA1‐dependent cristae modulation is essential for cellular adaptation to metabolic demand | The EMBO Journal

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

Anti-OPA1 antibody (ab42364) | Abcam
Anti-OPA1 antibody (ab42364) | Abcam

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

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

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

Western blotting analysis of Drp1 and Opa1 after 24 and 72 hours of... |  Download Scientific Diagram
Western blotting analysis of Drp1 and Opa1 after 24 and 72 hours of... | Download Scientific Diagram

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

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