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Mutations in this gene are associated with susceptibility to schizophrenia and obsessive-compulsive disorder
Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency
Model Number HPLC-112210 Description Amber Glass Screw Thread Vials
Full name ISYNA1 rabbit polyclonal antibody Alternative names 50 μl/100 μl Reactivity rabbit polyclonal Applications WB
Method validation and CRO testing workflows
ATG5 rabbit monoclonal antibody MycGuard-1 Solution Mutations in this gene areSpecification Full name ATG5 rabbit monoclonal antibody Alternative names 50 l 100 l Reactivity rabbit monoclonal Applications WB, IF Host Rabbit Clone type rabbit monoclonal Target Background The protein encoded by this gene, in combination with autophagy protein 12, functions as an E1 like activating enzyme in a ubiquitin like conjugating system. The encoded protein is involved in several cellular processes, including autophagic vesicle formation,
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