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

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|subunit:Homodimer when inactive

STX1A encodes a member of the syntaxin superfamily

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.