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glass slides with imprinted 316 overlapping 15 residue peptides corresponding to sars-cov-2 s sequence  (JPT Peptide Technologies GmbH)

 
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    Structured Review

    JPT Peptide Technologies GmbH glass slides with imprinted 316 overlapping 15 residue peptides corresponding to sars-cov-2 s sequence
    Glass Slides With Imprinted 316 Overlapping 15 Residue Peptides Corresponding To Sars Cov 2 S Sequence, supplied by JPT Peptide Technologies GmbH, 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/slide+imprinter/sars+cov+2+peptide+pools/pm35468973-357-13-20
    Average 90 stars, based on 1 article reviews
    glass slides with imprinted 316 overlapping 15 residue peptides corresponding to sars-cov-2 s sequence - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Western Blot:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Positive Control:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Negative Control:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Immunopeptidomics:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Injection:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Expressing:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Control:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Derivative Assay:

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated in the presence of a protein transport inhibitor (Brefeldin A, Biolegend) for 16 hours at 37°C with 2 mg of PepMixTM SARSCoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 72 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: Vaccination against SARS-CoV-2 provides low-level cross-protection against common cold coronaviruses in mouse and non-human primate animal models.
    Article Snippet: PBMCs were stimulated with either SARS-CoV-2 or HCoV-229E peptide pools (JPT Peptide Technologies GmbH, Berlin, Germany).

    Article Title: Neutralizing Antibody and T-Cell Spike Targeted Responses Following Receipt of a Monovalent Omicron JN.1-Adapted mRNA COVID-19 Vaccine in Immunosuppressed and Healthy Individuals.
    Article Snippet: We evaluated homologous neutralizing antibody (NtAb) and T‐cell responses after receipt of a JN.1‐adapted mRNA vaccine in a mixed population comprising healthy controls (HC) (n= 15), end‐stage chronic kidney disease (CKD) patients (n= 17), and allogeneic hematopoietic stem cell transplant recipients (allo‐HCT) (n= 13).. Most participants (42/45) were SARS‐CoV‐ 2‐experienced at the time of immunological testing.. JN.1‐spike‐binding NtAbs were measured with a vesicular stomatitis virus pseudotype‐based neutralization assay, whereas interferon (IFN)‐γ‐producing spike‐directed CD4 or CD8 T‐cell frequencies were enumerated using flow cytometry for intracellular staining.

    Article Title: Compositions and methods of mRNA vaccines against novel coronavirus infection
    Article Snippet: Cells were then stimulated for 16 hours at 37° C. with 2 μg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) (JPT Peptide Technologies GmbH) or media alone as a negative control.

    Article Title: A bivalent COVID-19 mRNA vaccine elicited broad immune responses and protection against Omicron subvariants infection.
    Article Snippet: Two hundred fifty thousand (250,000) splenocyteswere added into the plates and stimulatedwith a SARS-CoV-2 spike peptide pools (15-mer peptides with 11 amino acids overlap covering the full-length spike of Wuhan-Hu-1, Omicron BA.4/BA.5, XBB.1.5, or JN.1, JPT Peptide Technologies GmbH, Berlin, Germany) at 1 μg/ml/peptide.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: Subsequently, the cells were stimulated for 72 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.

    Article Title: S6P mutation in Delta and Omicron variant spike protein significantly enhances the efficacy of mRNA COVID-19 vaccines.
    Article Snippet: The cells were stimulated for 16 hours at 37°C with 2 mg of PepMixTM SARS-CoV-2 (Spike B.1.617.2/ Delta) from JPT Peptide Technologies GmbH, while media alone served as a negative control.



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    ADA Technologies Inc glycan array imprinted on higher density nhs-activated slides
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    Matsunami Glass glass slide with a lattice imprinted on its surface
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    Agilent technologies microarray slide imprinted capture probes
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