|Datasheet||Specific References||Reviews||Related Products||Protocols|
The pGEM-T is 3kb in length, and contains the amplicin resistance gene, conferring selection of the plasmid in E. coli, and the ori site which is the bacterial origin of replication. The plasmid has multiple cloning sites as shown below. The coding sequence was inserted by TA cloning. Many E. coli strains are suitable for the propagation of this vector including JM109, DH5α and TOP10.
The coding sequence can be easily obtained by digesting the vector with proper restriction enzyme(s). The coding sequence can also be amplified by PCR with M13 primers, or primer pair SP6 and T7.
|Human SMPDL3A Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG13559-G-F|
|Human SMPDL3A Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG13559-G-H|
|Human SMPDL3A Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG13559-G-M|
|Human SMPDL3A Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG13559-G-N|
|Human SMPDL3A Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG13559-G-Y|
SMPDL3A gene is a novel liver X receptor (LXR) -regulated gene, with an LXR response element within its promoter. The induction of SMPDL3A is LXR-dependent and is restricted to human blood cells with no induction observed in mouse cellular systems. LXR α and LXRβ function as physiological sensors of cholesterol metabolites (oxysterols), regulating key genes involved in cholesterol and lipid metabolism. LXRs have been extensively studied in both human and rodent cell systems, revealing their potential therapeutic value in the contexts of atherosclerosis and inflammatory diseases. The LXR genome landscape has been investigated in murine macrophages but not in human THP-1 cells, which represent one of the frequently used monocyte/macrophage cell systems to study immune responses.