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

A pseudogene of this gene is found on chromosome Y

Activation of this receptor induces cell-cell adhesion

human MEGF9 shares 76% aa sequence identity with mouse MEGF9

is located approximately 25 kb away from CYP1A1 on chromosome 15

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,