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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 KRAS ORF mammalian expression plasmid, C-GFPSpark tag||HG12259-ACG|
|Human KRAS ORF mammalian expression plasmid, C-OFPSpark / RFP tag||HG12259-ACR|
|Human KRAS ORF mammalian expression plasmid, N-GFPSpark tag||HG12259-ANG|
|Human KRAS ORF mammalian expression plasmid, C-Flag tag||HG12259-CF|
|Human KRAS ORF mammalian expression plasmid, C-His tag||HG12259-CH|
|Human KRAS ORF mammalian expression plasmid, C-Myc tag||HG12259-CM|
|Human KRAS ORF mammalian expression plasmid, C-HA tag||HG12259-CY|
|Human KRAS ORF mammalian expression plasmid, N-Flag tag||HG12259-NF|
|Human KRAS ORF mammalian expression plasmid, N-His tag||HG12259-NH|
|Human KRAS ORF mammalian expression plasmid, N-Myc tag||HG12259-NM|
|Human KRAS ORF mammalian expression plasmid, N-HA tag||HG12259-NY|
|Human KRAS natural ORF mammalian expression plasmid||HG12259-UT|
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K-Ras belongs to the small GTPase superfamily, Ras family. As other members of the Ras family, K-Ras is a GTPase and is an early player in many signal transduction pathways. It is usually tethered to cell membranes because of the presence of an isoprenyl group on its C-terminus. K-Ras functions as a molecular on/off switch. Once it is turned on it recruits and activates proteins necessary for the propagation of growth factor and other receptors' signal, such as c-Raf and PI 3-kinase. It binds to GTP in the active state and possesses an intrinsic enzymatic activity which cleaves the terminal phosphate of the nucleotide converting it to GDP. Upon conversion of GTP to GDP, K-Ras is turned off. The rate of conversion is usually slow but can be sped up dramatically by an accessory protein of the GTPase activating protein class, for example RasGAP. In turn K-Ras can bind to proteins of the Guanine Nucleotide Exchange Factor class, for example SOS1, which forces the release of bound nucleotide. Subsequently, K-Ras binds GTP present in the cytosol and the GEF is released from ras-GTP. Besides essential function in normal tissue signaling, the mutation of a K-Ras gene is an essential step in the development of many cancers. Several germline K-Ras mutations have been found to be associated with Noonan syndrome and cardio-facio-cutaneous syndrome. Somatic K-Ras mutations are found at high rates in Leukemias, colon cancer, pancreatic cancer and lung cancer.