Stat4 Polyclonal Antibody, 20ul[BT-AP14541] Peptide Modification Mutations in SLC16A2 are the

Mutations in SLC16A2 are the cause of Allan-Herndon-Dudley syndrome

endonuclease) is a ubiquitously expressed nuclear protein

The protein encoded by this gene belongs to the lipocalin family

and a pseudogene of this gene is located on the long arm of chromosome 6

Measure MMP-9 levels in human samples and gain valuable insights into potential risks and benefits

Stat4 Polyclonal Antibody, 20ul[BT-AP14541] Peptide Modification Mutations in SLC16A2 are theThe protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is essential for mediating responses to IL12 in lymphocytes, and regulating the differentiation of T helper cells.