Stat3 Polyclonal Antibody, 20ul[BT-AP14538] Reagent Reservoirs Mutations in this gene cause

Mutations in this gene cause autosomal-recessive intellectual disability

which is an immunodeficiency characterized by the failure to produce mature B lymphocytes

indoxyl sulfate (IS) and 3-carboxy-4-methyl-5-propyl-2-furanpropionate (CMPF)

swelling of subcutaneous tissue of the face

Allele-specific regulation of FGFR2 mRNA expression with a mildly increased breast cancer risk has been reported

Stat3 Polyclonal Antibody, 20ul[BT-AP14538] Reagent Reservoirs Mutations in this gene causeThe 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