DPOG1 Polyclonal Antibody, 20ul Pipette Controller Defects in EIF2B4 are a

Defects in EIF2B4 are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy

By acting through a filamin-A/F-actin axis

Multiple transcript variants encoding different isoforms have been found for EIF2B4

Synbio Technologies also provides multiple fluorescent groups and quenchers at 3’

DPOG1 Polyclonal Antibody, 20ul Pipette Controller Defects in EIF2B4 are aMitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy