MYL6B Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification Expand your experiments and grow

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Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin

Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome

miscellaneous:The EU sequence has the INV (3) allotypic marker| Ala-45 and Val-83

MYL6B Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification Expand your experiments and growMyosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in both slow twitch skeletal muscle and in nonmuscle tissue. Alternative splicing results in multiple transcript variants.