LIS1 Rabbit Polyclonal Antibody, 20ul Cell Labeling & Imaging 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 separates the site of transcription initiation from protein coding sequence

Since this protein is not capable of binding DNA directly

Microtubule associated proteins regulate the stability of microtubules and control processes such as cell polarity/differentiation

LIS1 Rabbit Polyclonal Antibody, 20ul Cell Labeling & Imaging Mutations in this gene areThis locus was identified as encoding a gene that when mutated or lost caused the lissencephaly associated with Miller Dieker lissencephaly syndrome. This gene encodes the non catalytic alpha subunit of the intracellular Ib isoform of platelet activating factor acteylhydrolase a heterotrimeric enzyme that specifically catalyzes the removal of the acetyl group at the SN 2 position of platelet activating factor (identified as 1 O alkyl 2 acetyl sn