Rad51B Polyclonal Antibody, 50ul Monoclonal Antibodies Mutations in TEAD1 cause Sveinsson's

Mutations in TEAD1 cause Sveinsson's chorioretinal atrophy

which is involved in multiubiquitin chain assembly

a kringle domain and a proline-rich domain

transient neonatal diabetes mellitus type 3 (TNDM3)

The MAF bZIP transcription factor F encoded by MAFF is a basic leucine zipper (bZIP) transcription factor that lacks a transactivation domain

Rad51B Polyclonal Antibody, 50ul Monoclonal Antibodies Mutations in TEAD1 cause Sveinsson'sThe protein encoded by RAD51B (RAD51 paralog B) is a member of the RAD51 protein family. RAD51 family members are evolutionarily conserved proteins essential for DNA repair by homologous recombination. This protein has been shown to form a stable heterodimer with the family member RAD51C, which further interacts with the other family members, such as RAD51, XRCC2, and XRCC3. Overexpression of RAD51B was found to cause cell cycle G1 delay and cell