Anti-Fyn (FYN, SLK, SYN, MGC45350, FYN oncogene related to SRC, FGR, YES, src-like kinase, c-syn pro

Alternate Name: FYN, SLK, SYN, MGC45350, FYN oncogene related to SRC, FGR, YES, src-like kinase, c-syn protooncogene, tyrosine kinase p59fyn(T), src/yes-related novel gene, OKT3-induced calcium influx regulator, proto-oncogene tyrosine-protein kinase fyn, Domain Information: Eukaryotic protein kinase domain, SH3 domain, Serine/Threonine protein kinases, catalytic domain, Src homology 2 domains, Src homology 3 domains, Src homology domain 2, Tyrosine kinase, catalytic domain , Gene Ontology Terms: learning, feeding behavior, protein kinase cascade, protein phosphorylation, protein tyrosine kinase, Application(s): Peptide ELISA: antibody detection limit dilution 1:32,000. Western Blot: Approx 55-60kD band observed in Jurkat, A431 and NIH-3T3 lysates (predicted MW of 62kD according to NP_002028.1). Recommended for use at 0.2-1ug/ml. Staining 0.2ug/ml) of Jurkat lysate (RIPA buffer, 35ug total protein per lane). Primary incubated for 1 hour. Detected by western blot using chemiluminescence. Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot and store at -20°C. Aliquots are stable for at least 12 months at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. Peptide Blocking: Corresponding peptide is available for Peptide Blocking studies. See F9500-03C-P. Antibody is typically 0.5mg/ml and peptide is supplied as a 100ul pellet. When peptide is reconstituted in 200ul water, the concentration would also be 0.5mg/ml. To start, the best ratio would be 1:1 (molar excess of peptide relative to antibody when identical volumes are mixed). Mix equal volumes of peptide and antibody at the required dilution and leave at ambient temperature. It is best is to have two identical blots to be incubated with equal amount of antibody, but one with the antibody pre-adsorbed to the peptide for 20min. Then incubate and develop the two blots in parallel.