PEG3 Polyclonal Antibody, 100ul Cell Culture Dishes and is able to complement

and is able to complement the yeast cdc42-1 mutant

Also component of the mSin3A complex which acts to repress transcription by deacetylation of nucleosomal histones

Mutations in this gene have been associated with hypokalemic periodic paralysis

An aberrant form of this protein has been detected in patients with Alzheimer's disease and Down syndrome

This family member functions in the translocation of peptides from the cytosol into the lysosomal lumen

PEG3 Polyclonal Antibody, 100ul Cell Culture Dishes and is able to complementIn human, ZIM2 and PEG3 are treated as two distinct genes though they share multiple 5' exons and a common promoter and both genes are paternally expressed (PMID: 15203203). Alternative splicing events connect their shared 5' exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. In contrast, in other mammals ZIM2 does not undergo imprinting and, in mouse, cow, and likely other mammals as well, the ZIM2