|Datasheet||Specific References||Reviews||Related Products||Protocols|
|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive, Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
A myc tag can be used in many different assays that require recognition by an antibody. If there is no antibody against the studied protein, adding a myc-tag allows one to follow the protein with an antibody against the Myc epitope. Examples are cellular localization studies by immunofluorescence or detection by Western blotting.
The peptide sequence of the myc-tag is: N-EQKLISEEDL-C (1202 Da). It can be fused to the C-terminus and the N-terminus of a protein. It is advisable not to fuse the tag directly behind the signal peptide of a secretory protein, since it can interfere with translocation into the secretory pathway.
|Mouse APOE ORF mammalian expression plasmid, C-GFPSpark tag||MG51201-ACG|
|Mouse APOE ORF mammalian expression plasmid, C-OFPSpark / RFP tag||MG51201-ACR|
|Mouse APOE ORF mammalian expression plasmid, C-Flag tag||MG51201-CF|
|Mouse APOE ORF mammalian expression plasmid, C-His tag||MG51201-CH|
|Mouse APOE ORF mammalian expression plasmid, C-Myc tag||MG51201-CM|
|Mouse APOE ORF mammalian expression plasmid, C-HA tag||MG51201-CY|
|Mouse APOE ORF mammalian expression plasmid, N-Flag tag||MG51201-NF|
|Mouse APOE ORF mammalian expression plasmid, N-His tag||MG51201-NH|
|Mouse APOE ORF mammalian expression plasmid, N-Myc tag||MG51201-NM|
|Mouse APOE ORF mammalian expression plasmid, N-HA tag||MG51201-NY|
|Mouse APOE Gene cDNA clone plasmid||MG51201-U|
|Mouse APOE natural ORF mammalian expression plasmid||MG51201-UT|
|Learn more about expression Vectors|
Apolipoprotein E (ApoE) is a 34.2 kDa glycosylated protein with 299 amino acid residues. There are three isoforms in human (apoE2, apoE3, and apoE4) due to different amino acid residues at positions 112 and 158. ApoE is synthesized predominantly in the liver, but also by cells in the spleen, brain, lung, kidney, ovary, adrenal, and muscle tissues. Hepatic parenchyma cells are the main apoE producing cells in mammalian body, probably accounting for two thirds to three fourths of the plasma apoE . In the nervous system, apoE mRNA is present in neurons, astrocytes, ependymal cells, nonmyelinating Schwann cells, but not in microglia, oligodendroglia, choroidal cells, or myelinating Schwann cells. ApoE produced by mammalian cells exists in different forms, monomers, dimers, modified, unmodified, lipid-rich, and lipid-poor, and so forth. ApoE plays a double-role in immune responses. Both apoE containing lipoproteins and multimers of synthetic apoE peptides inhibited proliferation of cultured lymphocytes by inhibiting DNA synthesis and reducing phospholipid turnover in T cells. ApoE can also affect innate and acquired immune responses in vitro by its ability to suppress stimulation of cultured neutrophils. ApoE can bind lipopolysaccharide (LPS), attenuate the inflammatory response, and thus reduce LPS induced lethality. Injection of LPS stimulated higher expression of inflammatory cytokines like interleukin (IL)-1β, IL-12, and interferon-γ (IFN-γ), as well as IL-6.