PXK Rabbit Polyclonal Antibody, 20ul Pipette Micro Tips which shows substantial homology to

which shows substantial homology to Ca2+/calmodulin-dependent protein kinase

10-methylenetetrahydrofolate to 5-methyltetrahydrofolate

Mediates pleiotropic functions among others in the cardiovascular

The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme

and the synaptosomal-associated protein SNAP25 are the main components of a protein complex involved in the docking and/or fusion of synaptic vesicles with the presynaptic membrane

PXK Rabbit Polyclonal Antibody, 20ul Pipette Micro Tips which shows substantial homology toThis gene encodes a phox (PX) domain containing protein which may be involved in synaptic transmission and the ligand induced internalization and degradation of epidermal growth factors. Variations in this gene may be associated with susceptibility to systemic lupus erythematosus (SLE). Alternative splicing results in multiple transcript variants.