XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation it is thought to play

it is thought to play a role in nitric oxide and polyamine metabolism

ephrin-A2 (ELF-1) has been described as the ligand for EphA4

Mutations in TUFM have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy

SLC52A2 (solute carrier family 52 member 2) encodes a membrane protein which belongs to the riboflavin transporter family

and thus represents a receptor-type PTP

XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation it is thought to playDNA repair protein XRCC4 encoded by XRCC4 functions together with DNA ligase IV and the DNA dependent protein kinase in the repair of DNA double strand breaks. This protein plays a role in both non homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternative splicing generates several transcript variants.