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DCAF8 encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Additionally we are shipping DCAF8 Antibodies (9) and DCAF8 Proteins (4) and many more products for this protein.
DCAF8 p.R317C mutation is responsible for specific variety of HMSN2 with infrequent giant axons and mild cardiomyopathy.
WDR42A is a nucleocytoplasmic shuttling protein.
while RNF10 (show RNF10 ELISA Kits) and WDR42A or VP22 alone showed distinct subcellular localization patterns, RNF10 (show RNF10 ELISA Kits) and WDR42A were relocated when co-expressed with VP22 or its homologues; these potential host cell factors of VP22 might expand the list of host targets of VP22
This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddb1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have been found for this gene.
DDB1 and CUL4 associated factor 8
, WD repeat domain 42A
, DDB1- and CUL4-associated factor 8
, WD repeat-containing protein 42A