R4RL1 Polyclonal Antibody, 20ul Hepatocytes Mutations in this gene that

Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I)

Sec7 and coiled-coil domains) family

EPAS1 encodes a transcription factor involved in the induction of genes regulated by oxygen

Apolipoprotein C-III is a very low density lipoprotein (VLDL) protein

R4RL1 Polyclonal Antibody, 20ul Hepatocytes Mutations in this gene thatMay play a role in regulating axonal regeneration and plasticity in the adult central nervous system.,Belongs to the Nogo receptor family.,Contains 8 LRR (leucine rich) repeats.,subcellular location: Localized to the surface of neurons, including axons.,tissue specificity: Predominantly expressed in brain. Expressed at lower levels in kidney, lung, mammary gland, placenta, salivary gland, skeletal muscle and spleen.,