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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.
|Cynomolgus monkey CD1B Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||CG90173-G-F|
|Cynomolgus monkey CD1B Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||CG90173-G-H|
|Cynomolgus monkey CD1B Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||CG90173-G-M|
|Cynomolgus monkey CD1B Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||CG90173-G-N|
|Cynomolgus monkey CD1B Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||CG90173-G-Y|
CD1B contains 1 Ig-like (immunoglobulin-like) domain and belongs to the CD1 family. CD1 family members are transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. During protein synthesis and maturation, they bind endogenous lipids that are replaced by lipid or glycolipid antigens when the proteins are internalized and pass through endosomes, before trafficking back to the cell surface. CD1B localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail, and requires vesicular acidification to bind lipid antigens.. It is expressed on cortical thymocytes, epidermal Langerhans cells, dendritic cells, on certain T-cell leukemias, and in various other tissues. CD1B is an antigen-presenting protein that binds self and non-self lipid and glycolipid antigens and presents them to T-cell receptors on natural killer T-cells.