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The encoded gene product presumably interacts with YY1 protein\; however, its exact function is not known. Additionally we are shipping YY1AP1 Antibodies (22) and and many more products for this protein.
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Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease.
YY1AP1 may serve as a key molecular target for EpCAM (show EPCAM Proteins)(+) AFP (show AFP Proteins)(+) HCC (show FAM126A Proteins) subtype
YY1AP is a novel co-activator of YY1 (show YY1 Proteins)
HCCA2 (show MOB2 Proteins) may play a novel role in cell cycle regulation.
The encoded gene product presumably interacts with YY1 protein\; however, its exact function is not known. Alternative splicing results in multiple transcript variants encoding different isoforms.
YY1-associated protein 1
, YY1 associated protein 1
, Dingo protein
, hepatocellular carcinoma susceptibility protein
, hepatocellular carcinoma-associated protein 2