RASF9 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Mutations in this gene are

Mutations in this gene are the cause of hyperlipoproteinemia| type 1D

It contains a C4-type zinc finger domain that can bind to zinc

Polymorphisms in this gene are associated with bipolar disorder and risk for schizophrenia

SRC-family kinases are recruited to the phosphorylated sites and can phosphorylate other tyrosine residues

this 100 mL solution is ideal for those willing to take risks and achieve maximum results

RASF9 Rabbit Polyclonal Antibody, 20ul Antibody Humanization Mutations in this gene areThe protein encoded by this gene localizes to perinuclear endosomes. This protein associates with peptidylglycine alpha amidating monooxygenase and may be involved with the trafficking of this enzyme through secretory or endosomal pathways.