RPAP2 Polyclonal Antibody, 100ul Pasteur Pipets a rare autosomal recessive lipid

a rare autosomal recessive lipid storage disease

This protein binds to an extended groove that is formed by the interaction of CBF1

a transcriptional regulator of immunoglobulin genes

the encoded protein is localized to the apical membrane and prevents excretion of glycerol into urine

RPAP2 Polyclonal Antibody, 100ul Pasteur Pipets a rare autosomal recessive lipidPutative RNA polymerase II subunit B1 C terminal domain (CTD) phosphatase that forms an interface between the RNA polymerase II enzyme and chaperone scaffolding protein, suggesting that it is required to connect RNA polymerase II to regulators of protein complex formation.