XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation EIF1AY (eukaryotic translation initiation factor

EIF1AY (eukaryotic translation initiation factor 1A

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

a member of the thyroid-steroid hormone receptor superfamily of nuclear transcriptional regulators

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

XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation EIF1AY (eukaryotic translation initiation factorDNA 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.