FoxR1 Polyclonal Antibody, 50ul Vector Construction Defects in PEX19 are a

Defects in PEX19 are a cause of Zellweger syndrome (ZWS)

making it a potential candidate for therapeutic stem cell expansion

This record represents the most centromeric copy which is in intron 22 of the F8 gene

subunit:Interacts with RENT2

This gene encodes a large multidomain protein of the phosphoinositide 3-kinase-related kinases (PIKK) family

FoxR1 Polyclonal Antibody, 50ul Vector Construction Defects in PEX19 are aFOXR1 encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix turn helix proteins with a core DNA binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. Forkhead box protein R1 lacks the C terminal basic region found in many other FOX family members. It is located within the 11q23. 3 region which is commonly