|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.
|Rat LILRA5 Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||RG80334-G-F|
|Rat LILRA5 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||RG80334-G-H|
|Rat LILRA5 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||RG80334-G-M|
|Rat LILRA5 Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||RG80334-G-N|
|Rat LILRA5 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||RG80334-G-Y|
LILRA5 is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LILR are a family of receptors possessing extracellular immunoglobulin domains. They are also known as CD85, ILTs and LIR, and can exert immunomodulatory effects on a wide range of immune cells. ILT-11 contains 2 Ig-like C2-type (immunoglobulin-like) domains. It can be detected n tissues of the hematopoietic system, including bone marrow, spleen, lymph node and peripheral leukocytes. Crosslink of ILT-11 on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses.