BCL3 Polyclonal Antibody, 100ul Cell Biology ETS family members have a

ETS family members have a highly conserved 85-amino acid ETS domain that binds purine-rich DNA sequences

and the truncated form additionally interacts with CCR1 and CCR2

also known as autosomal dominant speech and language disorder with orofacial dyspraxia

This autosomal dominant disorder is characterized by abnormal water reabsorption by kidney tubules due

This gene is localized to chromosome 8q22 which is disrupted in a variety of cancers

BCL3 Polyclonal Antibody, 100ul Cell Biology ETS family members have aThis gene is a proto oncogene candidate. It is identified by its translocation into the immunoglobulin alpha locus in some cases of B cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co activator that activates through its association with NF kappa B homodimers. The expression of this gene can be induced by NF