Product DescriptionMouse anti-Signal transducer and activator of transcription 3 Monoclonal Antibody (Unconjugated), suitable for WB, ELISA.
Application(s)ELISA, WB
Application DetailsThis antibody is recommended for WB and ELISA. Biosensis recommends optimal dilutions/concentrations should be determined by the end user.
TargetSignal transducer and activator of transcription 3
SpecificitySpecificity has been confirmed by WB and direct ELISA against the antigen. Human. Other species have not been tested.
Target Host SpeciesHuman
Species ReactivityHuman
Antibody HostMouse
Antibody TypeMonoclonal
Antibody IsotypeIgG
Clone Name1D11
ConjugateUnconjugated
Immunogen DescriptionRecombinant human Acute-phase response factor with GST tag.
Purity DescriptionProtein G purified immunoglobulin
FormatLyophilized from PBS pH 7.2
Reconstitution InstructionsSpin vial briefly before opening. Reconstitute in 100 µL sterile-filtered, ultrapure water. Centrifuge to remove any insoluble material.
Storage InstructionsAfter reconstitution keep aliquots at -20°C for higher stability. Glycerol (1:1) may be added for additional stability. Avoid repetitive freeze/thaw cycles.
Batch NumberPlease see item label.
Expiration Date12 months after date of receipt (unopened vial).
Alternative NamesSignal transducer and activator of transcription 3; STAT3; APRF
Acute-phase response factor is a transcription factor that binds to the IL-6-responsive elements identified in the promoters of various acute-phase protein genes. This protein is activated through phosphorylation in response to various cytokines and growth factors including IFNs, EGF, IL5, IL6, HGF, LIF and BMP2. Once phosphorylated, the protein is translocated into the nucleus. It forms a homodimer or a heterodimer with a related family member (STAT1). It is expressed in heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Defects in Acute-phase response factor are the cause of hyperimmunoglobulin E recurrent infection syndrome autosomal dominant (AD-HIES). This disorder is characterised by immunodeficiency, chronic eczema, recurrent Staphylococcal infections, increased serum IgE, eosinophilia, distinctive coarse facial appearance, abnormal dentition, hyperextensibility of the joints, and bone fractures.