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pMD18-T Simple Vector is a high-efficiency TA cloning vector constructed from pUC18, of which the initial multiple cloning sites (MCS) were destroyed. Thus the cDNA should be amplified by PCR with primers containing a restriction site for subclone. Competent cells appropriate for pUC18 are also appropriated for the Vector, e.g. JM109, DH5α, TOP10. The pMD18-T Simple Vector is 2.6kb in size. Selection of the plasmid in E. coli is conferred by the ampicillin resistance gene. The coding sequence was inserted by TA cloning at site 425.
The coding sequence can be amplified by PCR with M13-47 and RV-M primers.
|Human LTBR / TNFRSF3 Gene cDNA Clone (full-length ORF Clone) expression ready, FLAG-tagged||HG10581-M-F|
|Human LTBR / TNFRSF3 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG10581-M-H|
|Human LTBR / TNFRSF3 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG10581-M-M|
|Human LTBR / TNFRSF3 Gene cDNA Clone (full-length ORF Clone) expression ready, untagged||HG10581-M-N|
|Human LTBR / TNFRSF3 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG10581-M-Y|
LTBR (lymphotoxin beta receptor (TNFR superfamily, member 3)) is a member of the tumor necrosis factor (TNF) family of receptors. Tumor necrosis factor receptor is a trimeric cytokine receptor that binds tumor necrosis factors. The receptor cooperates with an adaptor protein (such as TRADD, TRAF, RIP), which is important in determining the outcome of the response. LTBR is expressed on the surface of most cell types, including cells of epithelial and myeloid lineages, but not on T and B lymphocytes. LTBR specifically binds the lymphotoxin membrane form (a complex of lymphotoxin-alpha and lymphtoxin-beta). LTBR and its ligand play a role in the development and organization of lymphoid tissue and tranformed cells. Activation of this protein can trigger apoptosis. Not only does the LTBR help trigger apoptosis, it can lead to the release of the cytokine interleukin 8. Overexpression of LTBR in HEK293 cells increases IL-8 promoter activity and leads to IL-8 release. It is also essential for development and organization of the secondary lymphoid organs and chemokine release.