CLSPN Polyclonal Antibody, 100ul Culture Plate Inserts SLC8 subfamily

SLC8 subfamily

Defects in GJC2 are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1

which is involved in large ribosomal subunit biogenesis

is a nuclear receptor protein that in humans is encoded by the THRB gene

Desmosome Associated Protein) is a Protein Coding gene

CLSPN Polyclonal Antibody, 100ul Culture Plate Inserts SLC8 subfamilyThe product of this gene is an essential upstream regulator of checkpoint kinase 1 and triggers a checkpoint arrest of the cell cycle in response to replicative stress or DNA damage. The protein is also required for efficient DNA replication during a normal S phase. Multiple transcript variants encoding different isoforms have been found for this gene.