Stat3 Monoclonal Antibody, 50ul[BT-MCA1162] Vessels tethering and fusion through interactions

tethering and fusion through interactions with small GTPases including Rab4

SESN1 encodes a member of the sestrin family

which encode distinct isoforms

Mutations in this gene are the cause of certain genetically-related cataract disorders

Certain mutations in this gene resulting in a functionally inadequate enzyme are associated with a rare genetic disorder causing nonspherocytic hemolytic anemia

Stat3 Monoclonal Antibody, 50ul[BT-MCA1162] Vessels tethering and fusion through interactionsThe protein encoded by this gene is a member of the STAT protein family. 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 through phosphorylation in response to various cytokines and growth factors including IFNs, EGF, IL5, IL6, HGF, LIF and