UT2 Rabbit Polyclonal Antibody, 50ul ssDNA Synthesis Defects in this gene could

Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

This protein is also a transcriptional co-repressor of androgen receptor-regulated genes and other cell cycle regulatory genes through its interactions with histone deacetylases

and is implicated in the transcriptional regulation of Hox genes and cytokines

Functional Modes: The DLAB pipette has four functional modes: liquid aspiration and dispensing

Four alternatively spliced transcript variants of MAPK14 encoding distinct isoforms have been reported

UT2 Rabbit Polyclonal Antibody, 50ul ssDNA Synthesis Defects in this gene couldThe protein encoded by this gene belongs to the urea transporter family. In mammalian cells urea is the chief end product of nitrogen catabolism and plays an important role in the urinary concentration mechanism. This protein is expressed in the inner medulla of the kidney and mediates rapid transepithelial urea transport across the inner medullary collecting duct. Alternatively spliced transcript variants have been found for this gene.