XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation a member of the thyroid-steroid

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

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 fibrillar collagen found in cartilage and the vitreous humor of the eye

IRAK1 encodes the interleukin-1 receptor-associated kinase 1

XRCC4 Polyclonal Antibody, 20ul Drug Development and Evaluation a member of the thyroid-steroidDNA 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.