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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.
|Human AK2 Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG13146-G-F|
|Human AK2 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG13146-G-H|
|Human AK2 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG13146-G-M|
|Human AK2 Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG13146-G-N|
|Human AK2 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG13146-G-Y|
Adenylate kinase 2 (AK2) belongs to the Adenylate kinase family that contains three isozymes: AK1, AK2 and AK3. Adenylate kinases are involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate groups among adenine nucleotides. Adenylate kinase2 (AK2) is expressed in mitochondrial intermembrane space. It may play a role in apoptosis. It has been demonstrated that in apoptotic cells AK2 was translocated into the cytosol concomitantly with cytochronme C. Mutations in this gene are the cause of reticular dysgenesis. These mutations result in absent or strongly decreased protein expression. It has been also established that AK2 is specifically expressed in the stria vascularis region of the inner ear, which provides an explanation of the sensorineural deafness in these individuals.