ELOVL6 Polyclonal Antibody, 20ul Molecular Weight Markers Mutations in this gene are

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

which comprises the proton channel

Members of the subfamily share similarity in sequence and splice sites

while the natural color allows for easy identification

membrane-associated glycoproteins

ELOVL6 Polyclonal Antibody, 20ul Molecular Weight Markers Mutations in this gene areFatty acid elongases (EC 6. 2. 1. 3), such as ELOVL6, use malonyl CoA as a 2 carbon donor in the first and rate limiting step of fatty acid elongation (Moon et al., 2001 [PubMed 11567032]).