SETMAR Polyclonal Antibody, 20ul Culture Tubes Specific mutations in DYSF have

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

not easy to break

KCNIP3 encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins

The extracellular domain of NG2 sequesters growth factors and binds to both growth factor receptors and extracellular matrix ligands such as fibronectin

SETMAR Polyclonal Antibody, 20ul Culture Tubes Specific mutations in DYSF haveSETMAR (SET domain and mariner transposase fusion gene) encodes a fusion protein that contains an N terminal histone lysine N methyltransferase domain and a C terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. SETMAR exists as a fusion