BCL3 Polyclonal Antibody, 100ul Cell Biology This autosomal dominant disorder is

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

is found in mature neurons and cells of neuronal origin

and the truncated form additionally interacts with CCR1 and CCR2

Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness

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

BCL3 Polyclonal Antibody, 100ul Cell Biology This autosomal dominant disorder isThis 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