PRPF31 Polyclonal Antibody, 100ul Peptide Synthesis The protein activates STK11 leading

The protein activates STK11 leading to the phosphorylation of both proteins and excluding STK11 from the nucleus

axon growth

Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3)

is associated with clathrin

Its expression has also been detected in developing CNS and testis and so the encoded protein may also play a role in neural development and spermatogenesis

PRPF31 Polyclonal Antibody, 100ul Peptide Synthesis The protein activates STK11 leadingPRPF31 encodes a component of the spliceosome complex and is one of several retinitis pigmentosa causing genes. When the gene product is added to the spliceosome complex, activation occurs.