Peroxin 10 Polyclonal Antibody, 20ul ssDNA Synthesis This gene encodes a DNA

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

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

which predominantly produces full-length

Volume Range: The MicroPette Plus offers a volume range of 0

Peroxin 10 Polyclonal Antibody, 20ul ssDNA Synthesis This gene encodes a DNAPEX10 (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.