MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing STX1A encodes a member of

STX1A encodes a member of the syntaxin superfamily

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

The complex| consisting of two alpha and four beta subunits| forms a double beta barrel assembly with six protruding coiled-coils

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

MNX1 Polyclonal Antibody, 20ul Microbial Genome Editing STX1A encodes a member ofThis 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.