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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.
|Rat ICAM2 ORF mammalian expression plasmid, C-GFPSpark tag||RG80239-ACG|
|Rat ICAM2 ORF mammalian expression plasmid, C-OFPSpark / RFP tag||RG80239-ACR|
|Rat ICAM2 ORF mammalian expression plasmid, C-Flag tag||RG80239-CF|
|Rat ICAM2 ORF mammalian expression plasmid, C-His tag||RG80239-CH|
|Rat ICAM2 ORF mammalian expression plasmid, C-Myc tag||RG80239-CM|
|Rat ICAM2 ORF mammalian expression plasmid, C-HA tag||RG80239-CY|
|Rat ICAM2 ORF mammalian expression plasmid, N-Flag tag||RG80239-NF|
|Rat ICAM2 ORF mammalian expression plasmid, N-His tag||RG80239-NH|
|Rat ICAM2 ORF mammalian expression plasmid, N-Myc tag||RG80239-NM|
|Rat ICAM2 ORF mammalian expression plasmid, N-HA tag||RG80239-NY|
|Rat ICAM2 natural ORF mammalian expression plasmid||RG80239-UT|
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Intercellular adhesion molecule 2 (ICAM-2, CD102), belongs to the ICAM family consisting of three members identified as ligands for integrin receptors. It is a type I transmembrane glycoprotein with two Ig-like C2-type domains, and binds to the leukocyte integrins LFA-1 (CD11a/CD18) and Mac-1 (CD11b/CD18). As a second ligand of leukocyte function-associated antigen-1, ICAM-2 functions as a costimulatory molecule for effector cells. ICAM-2 is mainly expressed on vascular endothelial and hematopoietic cells. Interactions of ICAM-2 and the integrin receptors mediate cell adhesion in a wide range of lymphocyte, monocyte, natural killer cell, and granulocytewith other cells, and play important roles in many adhesion-dependent immune and inflammation responses, such as T cell aggregation, NK-cell cytotoxicity and migration, lymphocyte recirculation, etc. Serum levels of ICAM-2 correlated significantly with the inflammatory and course sequences of trichinosis in mice and had a similar relation with blood eosinophilia. So, estimation of ICAM-2 serum levels may prove useful in diagnosis of trichinosis recent infections, and in monitoring the prognosis and response to treatment.