p53 Rabbit Polyclonal Antibody, 50ul[BT-AP11724] Contamination Detection & Removal Mutations in ACTA1 cause nemaline

Mutations in ACTA1 cause nemaline myopathy type 3

Note that the integrin alpha 5 and integrin alpha V subunits are encoded by distinct genes

TUBB3 encodes a class III member of the beta tubulin protein family

The encoded protein has additionally been identified to have uracil DNA glycosylase activity in the nucleus

Deficiencies in N-acetylglutamate synthase have been associated with hyperammonemia

p53 Rabbit Polyclonal Antibody, 50ul[BT-AP11724] Contamination Detection & Removal Mutations in ACTA1 cause nemalineThis gene encodes a tumor suppressor protein containing transcriptional activation DNA binding and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes thereby inducing cell cycle arrest apoptosis senescence DNA repair or changes in metabolism. Mutations in this gene are associated with a variety of human cancers including hereditary cancers such as Li Fraumeni syndrome. Alternative