ELOVL6 Polyclonal Antibody, 20ul Molecular Weight Markers which comprises the proton channel

which comprises the proton channel

membrane-associated glycoproteins

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

AQP1 is a possible candidate for disorders involving imbalance in ocular fluid movement

ELOVL6 Polyclonal Antibody, 20ul Molecular Weight Markers which comprises the proton channelFatty 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]).