Stat5a Polyclonal Antibody, 100ul[BT-AP08640] Cell Culture Mutations in SLC52A2 have been

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

MDD patients who also have a mutation in intron 2 of this gene show a significantly reduced response to citalopram as this antidepressant downregulates expression of this gene

human MEGF9 shares 76% aa sequence identity with mouse MEGF9

express MHC class II molecules and CD74 and act as APCs

with multiple epiphyseal dysplasia

Stat5a Polyclonal Antibody, 100ul[BT-AP08640] Cell Culture Mutations in SLC52A2 have beenThe protein encoded by STAT5A (signal transducer and activator of transcription 5A) 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 activated by, and mediates the responses of many cell ligands,