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 LIFR ORF mammalian expression plasmid, C-GFPSpark tag||RG80322-ACG|
|Rat LIFR ORF mammalian expression plasmid, C-OFPSpark / RFP tag||RG80322-ACR|
|Rat LIFR ORF mammalian expression plasmid, C-Flag tag||RG80322-CF|
|Rat LIFR ORF mammalian expression plasmid, C-His tag||RG80322-CH|
|Rat LIFR ORF mammalian expression plasmid, C-Myc tag||RG80322-CM|
|Rat LIFR ORF mammalian expression plasmid, C-HA tag||RG80322-CY|
|Rat LIFR ORF mammalian expression plasmid, N-Flag tag||RG80322-NF|
|Rat LIFR ORF mammalian expression plasmid, N-His tag||RG80322-NH|
|Rat LIFR ORF mammalian expression plasmid, N-Myc tag||RG80322-NM|
|Rat LIFR ORF mammalian expression plasmid, N-HA tag||RG80322-NY|
|Rat LIFR natural ORF mammalian expression plasmid||RG80322-UT|
|Learn more about expression Vectors|
LIFR (leukemia inhibitory factor receptor) belongs to the family of cytokine receptors. LIFR forms a high-affinity receptor complex with gp130, which mediates the activity of LIF (leukemia inhibitory factor) and thus affects the differentiation, proliferation, and survival of a wide variety of cells in the adult and the embryo. Besides LIF, LIFR can also bind to and activate CNTF (ciliary neurotrophic factor) and CLC (cardiotrophin like cytokine). Evidence showed that in the retina, LIFR activating LIF, CT-1 and cardiotrophin like cytokine (CLC) are strongly upregulated in response to preconditioning with bright cyclic light leading to robust activation of signal transducer and activator of transcription-3 (STAT3) in a time-dependent manner. Further, blocking LIFR activation during preconditioning using a LIFR antagonist (LIF05) attenuated the induced STAT3 activation and also resulted in reduced preconditioning-induced protection of the retinal photoreceptors. These data demonstrate that LIFR and its ligands play an essential role in endogenous neuroprotective mechanisms triggered by preconditioning-induced stress. LIFR was newly found to be a suppressor of hepatocellular carcinoma (HCC), one of the world's top five causes of cancer-related deaths.