STX16 Rabbit Polyclonal Antibody, 20ul Gene Synthesis Several transcript variants encoding different

Several transcript variants encoding different isoforms have been found for MARK3

flatness and other series of tests to ensure product quality

and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph

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

STX16 Rabbit Polyclonal Antibody, 20ul Gene Synthesis Several transcript variants encoding differentThis gene encodes a protein that is a member of the syntaxin or t SNARE (target SNAP receptor) family. These proteins are found on cell membranes and serve as the targets for V SNARES (vesicle SNAP receptors) permitting specific synaptic vesicle docking and fusion. A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib. Multiple transcript variants have been found for this