TSC-22 Polyclonal Antibody, 100ul Recombinant Protein Defects in PRF1 cause familial

Defects in PRF1 cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2)

Galanin is an important neuromodulator present in the brain

It is a member of the p160/steroid receptor coactivator (SRC) family and like other family members has histone acetyltransferase activity and contains a nuclear localization signal| as well as bHLH and PAS domains

SOD2 is a member of the iron/manganese superoxide dismutase family

TSC-22 Polyclonal Antibody, 100ul Recombinant Protein Defects in PRF1 cause familialTSC22D1 (TSC22 domain family member 1) encodes a member of the TSC22 domain family of leucine zipper transcription factors. The encoded protein is stimulated by transforming growth factor beta, and regulates the transcription of multiple genes including C type natriuretic peptide. The encoded protein may play a critical role in tumor suppression through the induction of cancer cell apoptosis, and a single nucleotide polymorphism in the promoter of