WTAP Polyclonal Antibody, 20ul PCR Series it also exhibits endonuclease activity

it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins

Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome

ABCA6 is clustered among 4 other ABC1 family members on 17q24 and may play a role in macrophage lipid homeostasis

CpG methylation is an epigenetic modification that is important for embryonic development

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WTAP Polyclonal Antibody, 20ul PCR Series it also exhibits endonuclease activityThe Wilms tumor suppressor gene WT1 appears to play a role in both transcriptional and posttranscriptional regulation of certain cellular genes. WTAP encodes a WT1 associating protein, which is a ubiquitously expressed nuclear protein. Like WT1 protein, pre mRNA splicing regulator WTAP is localized throughout the nucleoplasm as well as in speckles and partially colocalizes with splicing factors. Alternative splicing of this gene results in several