PCSK6 Rabbit Polyclonal Antibody, 50ul Drug Development and Evaluation Defects in this gene are

Defects in this gene are a cause of Zellweger syndrome (ZWS)

Natural killer (NK) cells express multiple calcium-dependent (C-type) lectin-like receptors

which alternatively utilize transferrin or non-transferrin iron delivery pathways

In addition to its water channel function

interacts with microtubules and is required for proper chromosome segregation and cytokinesis

PCSK6 Rabbit Polyclonal Antibody, 50ul Drug Development and Evaluation Defects in this gene areThis gene encodes a member of the subtilisin like proprotein convertase family which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the trans Golgi network where a second autocatalytic event takes place and the