FTCD Rabbit Polyclonal Antibody, 20ul Cell Culture Flasks a rare autosomal dominant proximal

a rare autosomal dominant proximal myopathy with early childhood onset

Defects in this gene are a cause of mitochondrial pyruvate carrier deficiency

Non-enzymatic cell harvesting solution to recover organoids/cells from hydrogel or an animal-based ECM within 15 minutes

in the conversion of tyrosine to melanin

The protein encoded by this gene is a member of the APBB protein family

FTCD Rabbit Polyclonal Antibody, 20ul Cell Culture Flasks a rare autosomal dominant proximalThe protein encoded by this gene is a bifunctional enzyme that channels 1 carbon units from formiminoglutamate a metabolite of the histidine degradation pathway to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.