DBP Polyclonal Antibody, 20ul Stepper Mutations in C9 cause component

Mutations in C9 cause component C9 deficiency

USP enzymes play critical roles in ubiquitin-dependent processes through polyubiquitin chain disassembly and hydrolysis of ubiquitin-substrate bonds

the gene is called COX1

and the protein is the target for neurodegeneration induced by organophosphorus compounds and chemical warfare agents

Suitable for 15 mL and 50 mL centrifuge tubes

DBP Polyclonal Antibody, 20ul Stepper Mutations in C9 cause componentThe protein encoded by this gene belongs to the albumin gene family. It is a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid and on the surface of many cell types. It binds to vitamin D and its plasma metabolites and transports them to target tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.