DYH5 Rabbit Polyclonal Antibody, 100ul Stepper an autosomal recessive disorder characterized

an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline

Overall rectangular structure

functionally different GSTP1 variant proteins that are thought to function in xenobiotic metabolism and play a role in susceptibility to cancer

With 30 ready-to-use reactions and a concentration of 1 rxn/μl

CSRP1 encodes a member of the cysteine-rich protein (CSRP) family

DYH5 Rabbit Polyclonal Antibody, 100ul Stepper an autosomal recessive disorder characterizedThis gene encodes a dynein protein which is part of a microtubule associated motor protein complex consisting of heavy light and intermediate chains. This protein is an axonemal heavy chain dynein. It functions as a force generating protein with ATPase activity whereby the release of ADP is thought to produce the force producing power stroke. Mutations in this gene cause primary ciliary dyskinesia type 3 as well as Kartagener syndrome which are both