UTP14A Polyclonal Antibody, 100ul Metabolic enzymes which serves as a light

which serves as a light chain

Mutations in this gene are associated with Nijmegen breakage syndrome| an autosomal recessive chromosomal instability syndrome characterized by microcephaly| growth retardation| immunodeficiency| and cancer predisposition

The encoded protein is present in all cell types and localized in plasma membranes and in intracellular vesicles

4 capacities available: 0

with high regularity

UTP14A Polyclonal Antibody, 100ul Metabolic enzymes which serves as a lightUTP14A encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the U3 small nucleolar RNA associated protein 14 homolog A is involved in ribosome biogenesis and 18S rRNA synthesis. An autosomal retrotransposed copy of this X linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.