CD56 Polyclonal Antibody, 100ul[BT-AP02415] Immunoassays The lack of RFX binding

The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al

More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases

Multimerin is a massive| soluble protein found in platelets and in the endothelium of blood vessels

Multiple transcript variants encoding distinct isoforms have been identified for this gene

DYNLRB2 (Dynein Light Chain Roadblock-Type 2) is a Protein Coding gene

CD56 Polyclonal Antibody, 100ul[BT-AP02415] Immunoassays The lack of RFX bindingCYP2U1 encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This enzyme is a hydroxylase that metabolizes arachidonic acid, docosahexaenoic acid, and other long chain fatty acids.