Peroxin 10 Polyclonal Antibody, 20ul ssDNA Synthesis The amino acid sequence consists

The amino acid sequence consists of predominantly hydrophobic N- and C-terminal regions

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3)

Multiple alternatively spliced transcript variants have been found

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This gene encodes a DNA methyltransferase which is thought to function in de novo methylation

Peroxin 10 Polyclonal Antibody, 20ul ssDNA Synthesis The amino acid sequence consistsPEX10 (peroxisomal biogenesis factor 10) encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.