FA72A Rabbit Polyclonal Antibody, 50ul Vector Construction 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

The encoded protein also functions as a calcium-regulated transcriptional repressor

Solute carrier family 25 proteins are localized to mitochondria and play critical roles in the transport of molecules across the inner mitochondrial membrane

This gene encodes a trypsin-like serine protease released from the submucosal serous glands onto mucous membrane

Black letter markings to help quickly identify and trace samples when manually adding samples

FA72A Rabbit Polyclonal Antibody, 50ul Vector Construction Mutations in this gene are