NKAP Polyclonal Antibody, 20ul Cell Biology TNF-alpha causes translocation from the

TNF-alpha causes translocation from the cytoplasm to the nucleus

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

This gene encodes a member of the epidermal growth factor receptor (EGFR) family of receptor tyrosine kinases

The product of MED13 is proposed to form a sub-complex with MED12

The gene encoding FAM84B maps to human chromosome 8

NKAP Polyclonal Antibody, 20ul Cell Biology TNF-alpha causes translocation from theThis gene encodes a protein that is involved in the activation of the ubiquitous transcription factor NF kappaB. This protein is associated with the the histone deacetylase HDAC3 and with the Notch corepressor complex, and it thereby acts as a transcriptional repressor of Notch target genes. It is also required for alphabeta T cell development. A related pseudogene has been identified on chromosome X, while a related and intronless retrocopy, which