Non-Mammalian ORFs
Sino Biological SARS-CoV-2 (2019-nCoV) Spike S2 Gene ORF cDNA clone expression plasmid, N-His tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(S2).
Sino Biological SARS-CoV-2 (2019-nCoV) Spike S2 Gene ORF cDNA clone expression plasmid, C-His tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(S2).
Cayman Chemical SARSCoVSARSCoV2 SpIke Gly 50uL
An a1-AR antagonist binds to a1-ARs in rat brain membranes (Ki 12.5 nM) inhibits a1-AR agonist-induced contractions in endothelium-denuded isolated rat aortic rings and perfused mesenteric vascular beds (pA2s 8.6 and 11.1 respectively) inhibits cirazoline-induced pressor responses in rats at 0.5 Ug/kg per minute i.v. improves postischemic glutamate uptake and reduces neuronal cell death and mortality in a rat model of global brain ischemia induced by mild hyperthermia at 32 mg/kg increases corneal NGF levels and accelerates corneal wound healing in a rat model of ocular injury
Sino Biological Human Coronavirus spike glycoprotein Gene ORF cDNA clone expression plasmid (Codon Optimized), N-Flag tag
Full length Clone DNA of Human coronavirus (isolate HKU1) Spike glycoprotein.
Sino Biological SARS-CoV-2 (2019-nCoV) Spike S1 Gene ORF cDNA clone expression plasmid, C-FLAG tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(S1).
Sino Biological SARS-CoV-2 (2019-nCoV) Spike S2 Gene ORF cDNA clone expression plasmid, C-FLAG tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(S2).
Sino Biological SARS-CoV-2 (2019-nCoV) Spike S1 ORF mammalian expression plasmid (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(S1).
ABclonal Technology HCoV-229E Spike S2 Rabbit mAb
S1 region attaches the virion to the cell membrane by interacting with host ANPEP aminopeptidase N initiating the infection Binding to the receptor probably induces conformational changes in the S glycoprotein unmasking the fusion peptide of S2 region and activating membranes fusion S2 region belongs to the class I viral fusion protein Under the current model the protein has at least 3 conformational states pre-fusion native state pre-hairpin intermediate state and post-fusion hairpin state During viral and target cell membrane fusion the coiled coil regions (heptad repeats regions assume a trimer-of-hairpins structure positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes
Sino Biological Human coronavirus(HCoV-NL63) Spike Gene ORF cDNA clone expression plasmid (Codon Optimized)
Full length Clone DNA of Human coronavirus (HCoV-NL63) Spike.
Sino Biological SARS-CoV-2 (2019-nCoV) Nucleoprotein Gene ORF cDNA clone expression plasmid, C-His tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Nucleoprotein / NP.
Cayman Chemical SARSCoVSARSCoV2 SpIke Gly 50uL
A quantitative analytical standard guaranteed to meet MaxSpec identity purity stability and concentration specifications
Sino Biological SARS-CoV-2 (2019-nCoV) Spike RBD Gene ORF cDNA clone expression plasmid, N-His tag (Codon Optimized)
Full length Clone DNA of SARS-CoV-2 (2019-nCoV) Spike(RBD).
ABclonal Technology HCoV-229E Spike S2 Rabbit mAb
S1 region attaches the virion to the cell membrane by interacting with host ANPEP aminopeptidase N initiating the infection Binding to the receptor probably induces conformational changes in the S glycoprotein unmasking the fusion peptide of S2 region and activating membranes fusion S2 region belongs to the class I viral fusion protein Under the current model the protein has at least 3 conformational states pre-fusion native state pre-hairpin intermediate state and post-fusion hairpin state During viral and target cell membrane fusion the coiled coil regions (heptad repeats regions assume a trimer-of-hairpins structure positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes