RPC6 Polyclonal Antibody, 100ul Recombinant Protein TPD52L1 (D53)

TPD52L1 (D53)

A splice-site mutation in this gene has been associated with a novel progressive myoclonic epilepsy disease with similar symptoms to MERRF syndrome

likely plays a role in non-homologous end joining and other DNA repair processes

Members of this family are part of a multisubunit complex that functions as a microtubule motor in intracellular organelle transport

This protein is thought to be be involved in multiple cellular processes| including maintenance of skin homeostasis| and suppression of invasiveness and metastasis

RPC6 Polyclonal Antibody, 100ul Recombinant Protein TPD52L1 (D53)The protein encoded by this gene is one of more than a dozen subunits forming eukaryotic RNA polymerase III (RNA Pol III), which transcribes 5S ribosomal RNA and tRNA genes. This protein has been shown to bind both TFIIIB90 and TBP, two subunits of RNA polymerase III transcription initiation factor IIIB (TFIIIB). Unlike most of the other RNA Pol III subunits, the encoded protein is unique to this polymerase. Alternative splicing results in multiple