ZN750 Polyclonal Antibody, 50ul RNA Synthesis Mutations in SLC22A5 (solute carrier

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

and SNAP25 interact to form the SNARE complex

Catalase converts the reactive oxygen species hydrogen peroxide to water and oxygen and thereby mitigates the toxic effects of hydrogen peroxide

designated Q20*) which blocks expression of this protein

as well as the STAT family

ZN750 Polyclonal Antibody, 50ul RNA Synthesis Mutations in SLC22A5 (solute carrierThis gene encodes a protein with a nuclear localization site and a C2H2 zinc finger domain. Mutations in this gene have been associated with seborrhea like dermatitis with psoriasiform elements.