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GenScript corporation codon-optimized spike sequences
Codon Optimized Spike Sequences, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/codon-optimized+spike+sequences/cpass+sars+cov+2+neutralization+antibody+detection+kit/pm39082740-56-2-8
Average 90 stars, based on 1 article reviews
codon-optimized spike sequences - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

other:

Article Title: Trajectory of humoral responses to two doses of the ChAdOx1 nCoV-19 vaccination in patients receiving maintenance hemodialysis
Article Snippet: A US-FDA-authorized sVNT assay (cPass SARS-CoV-2 Neutralization Antibody Detection Kit, GenScript, Singapore) was used to quantify neutralizing antibodies against ancestral virus, delta and omicron (BA.1) at V2M1 and V2M5.

Article Title: Targeting heptad repeats and fusion peptide: nanoparticle vaccine elicits mucosal immune response against SARS-CoV-2 variants.
Article Snippet: The following antibodies were used: CD19-BV510 (Biolegend 115546), IgD-PE (Biolegend 405706), CD38-R718 (BD 752576), IgG1-PECY7 (Invitrogen M1-14D12), IgG2a-FITC (BD 562028), Streptavidin-BV421 (BD 563259), IgA-FITC (Invitrogen mA-6E1), CD4-R718 (BD 566939), CD8-BV510 (BD 563068), CD69-PE-CY7 (BD 552879), CD103-BV421 (Biolegend 121422), CD44-FITC (Biolegend 103006), CD95-PE-CY7 (BD 557653), GL7-FITC (Biolegend 144604), CXCR5-Biotin (Biolegend 145510), PD-1-APC (Invitrogen RMP1-30).

Article Title: Evaluating the distribution and clustering of SARS-CoV-2 antibodies in dogs across the United States of America.
Article Snippet: Serum samples collected from household dogs in this study were tested using blocking enzyme-linked immunosorbent assay (bELISA)31, Serum neutralization (SN)7, LumitTM Dx SARS-CoV-2 Immunoassay (Promega, Madison, Wisconsin), and cPassTM SARS-CoV-2 Neutralization Antibody Detection Assay (GenScript, Piscataway, New Jersey).

Article Title: Evaluating the distribution and clustering of SARS-CoV-2 antibodies in dogs across the United States of America
Article Snippet: Serum samples collected from household dogs in this study were tested using blocking enzyme-linked immunosorbent assay (bELISA) , Serum neutralization (SN) , LumitTM Dx SARS-CoV-2 Immunoassay (Promega, Madison, Wisconsin), and cPassTM SARS-CoV-2 Neutralization Antibody Detection Assay (GenScript, Piscataway, New Jersey).

Article Title: Quantitative characterisation of extracellular vesicles designed to decoy or compete with SARS-CoV-2 reveals differential mode of action across variants of concern and highlights the diversity of Omicron.
Article Snippet: As shown in Supplementary Table 1c, two different assays were applied for anti-SARS-CoV-2 screening according to manufacturer’s instructions: the Elecsys Anti-SARS-CoV-2 total anti-N antibody ECLIA (Roche Diagnostics) and a SARS-CoV-2 Surrogate Virus Neutralization Test (sVNT) (GenScript, Piscataway Town-ship, New Jersey, USA) using an ETIMax3000 platform (Diasorin, Saluggia, Italy).

Article Title: Comparative analysis of humoral immunity kinetics following three COVID-19 vaccines in a multi-ethnic cohort of medical students and healthcare professionals across Malaysia.
Article Snippet: A02161 was utilized as the positive control when the SARS-CoV-2 Surrogate Virus Neutralization Test (sVNT) Kit (GenScript, Cat.No.

Inhibition:

Article Title: Compositions including Sbi adjuvants and methods of use thereof
Article Snippet: .. ACE2:RBD inhibition assay: The ability of vaccinated sera to inhibit ACE2:RBD binding was measured essentially as described in Nie, et al. (Nat Biotech 15: 3699-3715, 2020), using the SARS-CoV-2 Surrogate Virus Neutralization Test kit (GenScript). ..

Binding Assay:

Article Title: Compositions including Sbi adjuvants and methods of use thereof
Article Snippet: .. ACE2:RBD inhibition assay: The ability of vaccinated sera to inhibit ACE2:RBD binding was measured essentially as described in Nie, et al. (Nat Biotech 15: 3699-3715, 2020), using the SARS-CoV-2 Surrogate Virus Neutralization Test kit (GenScript). ..

Virus:

Article Title: Compositions including Sbi adjuvants and methods of use thereof
Article Snippet: .. ACE2:RBD inhibition assay: The ability of vaccinated sera to inhibit ACE2:RBD binding was measured essentially as described in Nie, et al. (Nat Biotech 15: 3699-3715, 2020), using the SARS-CoV-2 Surrogate Virus Neutralization Test kit (GenScript). ..

Neutralization:

Article Title: Compositions including Sbi adjuvants and methods of use thereof
Article Snippet: .. ACE2:RBD inhibition assay: The ability of vaccinated sera to inhibit ACE2:RBD binding was measured essentially as described in Nie, et al. (Nat Biotech 15: 3699-3715, 2020), using the SARS-CoV-2 Surrogate Virus Neutralization Test kit (GenScript). ..

Sequencing:

Article Title: HTRF-based identification of small molecules targeting SARS-CoV-2 E protein interaction with ZO-1 PDZ2
Article Snippet: .. The cDNA sequence encoding amino acids 45-75 of the SARS-CoV-2 E protein was synthesized and then cloned into the pET-15b vector by GenScript. ..

Synthesized:

Article Title: HTRF-based identification of small molecules targeting SARS-CoV-2 E protein interaction with ZO-1 PDZ2
Article Snippet: .. The cDNA sequence encoding amino acids 45-75 of the SARS-CoV-2 E protein was synthesized and then cloned into the pET-15b vector by GenScript. ..

Clone Assay:

Article Title: HTRF-based identification of small molecules targeting SARS-CoV-2 E protein interaction with ZO-1 PDZ2
Article Snippet: .. The cDNA sequence encoding amino acids 45-75 of the SARS-CoV-2 E protein was synthesized and then cloned into the pET-15b vector by GenScript. ..



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Thermo Fisher codon-optimized spike protein nucleotide sequence
a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled <t>S</t> <t>protein</t> regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.
Codon Optimized Spike Protein Nucleotide Sequence, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled <t>S</t> <t>protein</t> regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.
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a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled <t>S</t> <t>protein</t> regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.
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Thermo Fisher codon-optimized spike dna sequences
a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled <t>S</t> <t>protein</t> regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.
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GenScript corporation codon-optimized spike sequences
a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled <t>S</t> <t>protein</t> regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.
Codon Optimized Spike Sequences, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher codon optimized spike dna sequences for d614g

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GenScript corporation human codon-optimized sequences corresponding to the spike ectodomains of rtvn2129, rtvn21-192, rtvn21-193 and rtvn21-201

Human Codon Optimized Sequences Corresponding To The Spike Ectodomains Of Rtvn2129, Rtvn21 192, Rtvn21 193 And Rtvn21 201, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher human codon optimized sars-cov-2 spike sequence

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GenScript corporation human codon-optimized sequences of the ectodomain of sars-cov-2 spike protein, amino acid position 1-1,210

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Sino Biological sars cov 2 related sequences
Infectivity tested using compounds of K-4 and M-4 (10 μM) against pseudotyped virus (PV) of <t>SARS-CoV-2</t> Delta ( A , B ) or Omicron ( C , D ) variant with 10 μM dose of Lopinavir ( E ) as a positive control drug. Values indicate means ± SEM. ( n = 3, *** p < 0.001, **** < 0.0001 vs. control group)
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Image Search Results


a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled S protein regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.

Journal: Nature Communications

Article Title: Ultrapotent SARS coronavirus-neutralizing single-domain antibodies that clamp the spike at its base

doi: 10.1038/s41467-025-60250-1

Figure Lengend Snippet: a left: model of full-length prefusion S (6VSB_1_1_2 ) with superimposition of the R3DC23 – HR2 complex, all shown in molecular surface representation, with N-glycans in stick representation. R3DC23 VHHs are colored in orange, labeled S protein regions: cytoplasmic domain (red; CP), transmembrane domain (gray; TM), heptad repeat 2 (blue; HR2), S2 stem helix (deep pink; SH), heptad repeat 1 (lemon, HR1), central helix and connector domain (pink; CH-CD), the S1 regions encompassing the N-terminal domain (NTD) and receptor binding domain (RBD) (light blue). Right: model of the proteolytically processed postfusion S2 subunit (7E9T ), color coded as in prefusion spike. b Side and axial view (inset) of the R3DC23 – HR2 complex (sand and blue, respectively) superimposed with prefusion HR2 coiled-coil (light blue). In R3DC23, CDR1, 2, and 3 are colored magenta, yellow, and cyan, respectively. The HR2-binding epitope spanning D1192 – Y1206 is shown in stick representation. c Close-up of boxed region, encompassing a single VHH and two HR2 copies (i and ii) forming the adjoined binding epitope. Escape mutant positions are labeled in red. d Axial view of HR1-HR2 (lemon and blue) region of postfusion S protein, superimposed with R3DC23 in the HR2 complex (gray). e The amino acids involved in interactions between R3DC23 and two HR2 helices as observed in the crystal of the R3DC23-HR2 complex are indicated in red.

Article Snippet: For the pCG1-SARS-2-BA.2 Sdel18 expression vector, a codon-optimized spike protein nucleotide sequence containing the BA.2 mutations (T19I, ΔL14-P26, A27S, G142D, V213G, G339D, S371F, S373P, S375F, T376A, D405N, R408S, K417N, N440K, S477N, T478K, E484A, Q493R, Q498R, N501Y, Y505H, D614G, H655Y, N679K, P681H, N764K, D796Y, Q954H, N969K) and flanking BamH I and Sal I restriction sites was ordered at GeneArt (Thermo Fischer Scientific) and cloned in the pCG1 vector as a Bam HI/ Sal I fragment.

Techniques: Labeling, Binding Assay, Mutagenesis

Journal: iScience

Article Title: Immunogenicity of a third dose with mRNA-vaccines in the ChAdOx1-S/BNT162b2 vaccination regimen against SARS-CoV-2 variants

doi: 10.1016/j.isci.2024.110728

Figure Lengend Snippet:

Article Snippet: Codon-optimized spike DNA sequences for D614G, B.1.617.2, BA.1, BA.4/BA.5, BQ.1.1, XBB.1.5/XBB.1.9, BA.2.86, and JN.1 SARS-CoV-2 variants , GeneArt Gene Synthesis (ThermoFisher) , N/A.

Techniques: Recombinant, Luciferase, Software

Infectivity tested using compounds of K-4 and M-4 (10 μM) against pseudotyped virus (PV) of SARS-CoV-2 Delta ( A , B ) or Omicron ( C , D ) variant with 10 μM dose of Lopinavir ( E ) as a positive control drug. Values indicate means ± SEM. ( n = 3, *** p < 0.001, **** < 0.0001 vs. control group)

Journal: Biomaterials Research

Article Title: Development of a screening platform to discover natural products active against SARS-CoV-2 infection using lung organoid models

doi: 10.1186/s40824-023-00357-y

Figure Lengend Snippet: Infectivity tested using compounds of K-4 and M-4 (10 μM) against pseudotyped virus (PV) of SARS-CoV-2 Delta ( A , B ) or Omicron ( C , D ) variant with 10 μM dose of Lopinavir ( E ) as a positive control drug. Values indicate means ± SEM. ( n = 3, *** p < 0.001, **** < 0.0001 vs. control group)

Article Snippet: The SARS-CoV-2-related sequences were codon-optimized for human expression and purchased from Sino Biological (Beijing, China).

Techniques: Infection, Variant Assay, Positive Control

Transcriptome analysis and the cell type analysis in control (GFP) or pseudovirus of SARS-CoV-2 Omicron variant infected in human LOs ( n = 3). A Volcano plot of differentially expressed genes (DEGs) of PV-infected LO samples compared with control samples. Horizontal and vertical dashed blue lines indicate p -value < 0.05 and fold change = 4, respectively. Red dots indicate significant ( p -value < 0.05) DEGs. B Top 25 genes of significantly up- or downregulated DEGs. C Heatmap of enrichment with lung-related cell types in PV-infected LOs by referring to the CellMarker database. D Lung cell-specific markers whole-stained using LOs. LOs were fixed and analyzed with various cell-type markers through immunofluorescence and visualized through confocal microscopy. Scale bar: 20 μm

Journal: Biomaterials Research

Article Title: Development of a screening platform to discover natural products active against SARS-CoV-2 infection using lung organoid models

doi: 10.1186/s40824-023-00357-y

Figure Lengend Snippet: Transcriptome analysis and the cell type analysis in control (GFP) or pseudovirus of SARS-CoV-2 Omicron variant infected in human LOs ( n = 3). A Volcano plot of differentially expressed genes (DEGs) of PV-infected LO samples compared with control samples. Horizontal and vertical dashed blue lines indicate p -value < 0.05 and fold change = 4, respectively. Red dots indicate significant ( p -value < 0.05) DEGs. B Top 25 genes of significantly up- or downregulated DEGs. C Heatmap of enrichment with lung-related cell types in PV-infected LOs by referring to the CellMarker database. D Lung cell-specific markers whole-stained using LOs. LOs were fixed and analyzed with various cell-type markers through immunofluorescence and visualized through confocal microscopy. Scale bar: 20 μm

Article Snippet: The SARS-CoV-2-related sequences were codon-optimized for human expression and purchased from Sino Biological (Beijing, China).

Techniques: Variant Assay, Infection, Staining, Immunofluorescence, Confocal Microscopy

The anti-infective potential of K-4 ( A ) or M-4 ( B ) in the lung organoids infected with pseudotyped virus (PV) of SARS-CoV-2 Omicron variant. Values indicate means ± SEM. ( n = 3, **** < 0.0001 vs. control group)

Journal: Biomaterials Research

Article Title: Development of a screening platform to discover natural products active against SARS-CoV-2 infection using lung organoid models

doi: 10.1186/s40824-023-00357-y

Figure Lengend Snippet: The anti-infective potential of K-4 ( A ) or M-4 ( B ) in the lung organoids infected with pseudotyped virus (PV) of SARS-CoV-2 Omicron variant. Values indicate means ± SEM. ( n = 3, **** < 0.0001 vs. control group)

Article Snippet: The SARS-CoV-2-related sequences were codon-optimized for human expression and purchased from Sino Biological (Beijing, China).

Techniques: Infection, Variant Assay