TYRO3/DTK Protein, Cynomolgus (HEK293, His)

TYRO3/DTK Protein, Cynomolgus (HEK293, His) is the recombinant cynomolgus-derived TYRO3/DTK protein, expressed by HEK293, with C-His tag.

TYRO3/DTK is a receptor tyrosine kinase that transduces signals from the extracellular matrix to the cytoplasm by binding to several ligands, including TULP1 or GAS6. Regulates many physiological processes, including cell survival, migration, and differentiation. The binding of ligands on the cell surface induced dimerization and autophosphorylation of TYRO3 in the intracellular region, providing docking sites for downstream signaling molecules. After the ligand is activated, it interacts with PIK3R1 to enhance PI3 kinase activity. Activation of AKT survival pathway, including nuclear translocation of NF-kappa-B and up-regulation of NF-kappa-B regulatory genes. TYRO3 signaling plays a role in a variety of processes, such as neuronal protection from excitotoxic damage, platelet aggregation, and cytoskeletal recombination. By activating STAT1, which plays an important role in Toll-like receptor (TLRs) mediated innate immune response, STAT1 selectively induces the production of inhibitors of cytokine signaling pathways SOCS1 and SOCS3. TYRO3 is overexpressed in many types of cancer and has the function of promoting tumor cell survival and/or proliferation, metastasis, and chemotherapy resistance^[1][2].

Cynomolgus

HEK293

C-8*His

A0A2K5WCY8 (G41-S427)

/

Partial

GLKLMGAPVKLTVSQGQPVKLNCSVEGMEEPDIQWVKDGAVVQNLDQLYIPVSEQHWIGFLSLKSAERSDAGRYWCQVEDGGETEISQPVWLTVEGVPFFTVEPKDLAVPPNAPFQLSCEAVGPPEPVTIVWWRGTTKIGGPAPSPSVLNVTGVTQSTMFSCEAHNLKGLASSRTATVHLQALPAAPFNVTVTKLSSSNASVAWMPGADGRALLQSCTVQVTQAPGGWEVLAVVVPVPPFTCLLRDLVPATNYSLRVRCANALGPSPYADWVPFQTKGLAPASAPQNLHAIRTDSGLILEWEEVIPEGPLEGPLGPYKLSWVQDNGTQDELTVEGTRANLTGWDPQKDLIVRVCVSNAVGCGPWSQPLVVSSHDHAGQQGPPHSRTS

Approximately 50-70 kDa, based on SDS-PAGE under reducing conditions, due to the glycosylation.

≥ 95%, as determined by reducing SDS-PAGE.;≥ 95%, as determined by HPLC.

<1 EU/μg, determined by LAL method.