![Recombinant Anti-SUCLA2 antibody [EPR14925] (ab183513) | Abcam](https://www.abcam.com/ps/products/183/ab183513/Images/ab183513-215190-anti-sucla2-antibody-epr14925-western-blot.jpg "Recombinant Anti-SUCLA2 antibody [EPR14925] (ab183513) | Abcam")
Recombinant Anti-SUCLA2 antibody [EPR14925] (ab183513) | Abcam
SUCLA2 Fusion Protein Ag3319 | Proteintech
SUCLA2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech 20 μL; Unconjugated products | Fisher Scientific
Disorders caused by deficiency of succinate‐CoA ligase - Ostergaard - 2008 - Journal of Inherited Metabolic Disease - Wiley Online Library
Screening of small molecules that selectively kill SUCLA2-deleted... | Download Scientific Diagram
Depletion of mtDNA with MMA: SUCLA2 and SUCLG1 | SpringerLink
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
SUCLA2 CRISPR Knockout and Activation Products (m) | SCBT - Santa Cruz Biotechnology
SUCLA2 gene | Semantic Scholar
SUCLA2 gene | Semantic Scholar
SUCLA2-coupled regulation of GLS succinylation and activity counteracts oxidative stress in tumor cells - ScienceDirect
Anti-SUCLA2 Antibody | Rabbit anti-Human Polyclonal ICC,IHC,WB | LSBio
SUCLA2 Antibody (NBP1-33015): Novus Biologicals
進行前立腺がんの新しい治療薬を開発 – 金沢大学
IJMS | Free Full-Text | Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit
SUCLA2 antibody (12627-1-AP) | Proteintech
Relevant metabolic pathways illustrating the metabolic effects of... | Download Scientific Diagram
SUCLA2 Polyclonal Antibody, Invitrogen™ 100 μL; Unconjugated Products | Fisher Scientific
Cranial MRI of MDS. Cranial MRI of the patient with SUCLA2 mutation... | Download Scientific Diagram
Clinical and molecular features of mitochondrial DNA depletion syndromes - Spinazzola - 2009 - Journal of Inherited Metabolic Disease - Wiley Online Library
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 children - ScienceDirect
SUCLA2 mutations cause global protein succinylation contributing to the pathomechanism of a hereditary mitochondrial disease | Nature Communications
Thymoquinone targets SUCLA2 loss that collaterally takes place with RB1... | Download Scientific Diagram
