MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing which leads to the loss

which leads to the loss in membrane potential and the release of cytochrome c

The pleckstrin homology and RhoGEF domain containing G4 encoded by PLEKHG4 can function as a guanine nucleotide exchange factor (GEF) and may play a role in intracellular signaling and cytoskeleton dynamics at the Golgi apparatus

An important paralog of this gene is UBTD1

followed by a transmembrane domain and a short C-terminal cytoplasmic tail domain

highly hydrophobic N-terminal domain of 167 amino acids and a conserved C-terminal region of 299 amino acids

MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing which leads to the lossThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.