Rad18 Polyclonal Antibody, 100ul Hepatocytes This gene is a candidate

This gene is a candidate gene for autosomal dominant retinitis pigmentosa

Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT)

frontal cortex

one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome

The product of SMAD4 forms homomeric complexes and heteromeric complexes with other activated Smad proteins

Rad18 Polyclonal Antibody, 100ul Hepatocytes This gene is a candidateRAD18, E3 ubiquitin protein ligase encoded by RAD18 is highly similar to S. cerevisiae DNA damage repair protein Rad18. Yeast Rad18 functions through its interaction with Rad6, which is an ubiquitin conjugating enzyme required for post replication repair of damaged DNA. Similar to its yeast counterpart, RAD18, E3 ubiquitin protein ligase is able to interact with the human homolog of yeast Rad6 protein through a conserved ring finger motif. Mutation of