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  1. Concentration–response curves for binding of CoV2 spike protein to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of ACE2-Fc at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS and blocked with 200 µL of
    SARS-CoV-2 XBB.1.5/XBB.1.9.1 Omicron Variant Recombinant Spike Trimer His Tag
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  2. Concentration-response curves for binding of CoV2 spike protein XBB.1 variant to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of each spike trimer at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS an
    SARS-CoV-2 XBB.1/XBB.1.9 Omicron Variant recombinant Spike Trimer His Tag
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  3. Concentration–response curves for binding of CoV2 spike protein to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of ACE2-Fc at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS and blocked with 200 µL of
    SARS-CoV-2 XBF Omicron Variant Recombinant Spike Trimer His Tag
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  4. Concentration–response curves for binding of CoV2 spike protein to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of ACE2-Fc at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS and blocked with 200 µL
    SARS-CoV-2 XEC Omicron Variant Recombinant Spike Trimer His Tag
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  5. Concentration–response curves for binding of CoV2 spike protein XFG to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of ACE2-Fc at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS and blocked with 200
    SARS-CoV-2 XFG Omicron Variant Recombinant Spike Trimer His Tag
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  6. Affinity assessment of SARS-CoV-2 C-A11 IgG to wild type and B.1.1.7 (UK) S1+S2 trimers. C-A11 possesses very low (pM) KD affinity to both variants.
    SARS-CoV-2 spike protein (RBD) neutralizing (C-A11) rabbit mAb
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  7. Surrogate virus neutralization test (sVNT): ACE2 protein (Cat#2566) was coated at 2 ug/mL. CR3-C2 was serially diluted and incubated with 48 ng/mL of spike trimers at room temperature for 1 hour. The mixture was then added to blocked wells and incubated a
    SARS-CoV2 CR3-C2 human neutralizing mAb
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  8. SARS-CoV2 G10xA1 human neutralizing mAb
    SARS-CoV2 G10xA1 human neutralizing mAb
    From $210.00
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  9. SARS-CoV2 G10xA5 human neutralizing mAb
    SARS-CoV2 G10xA5 human neutralizing mAb
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  10. Spike protein trimers were coated at 2 µg/mL and incubated with serially diluted antibodies. The bound antibodies were detected with Peroxidase AffiniPure Goat Anti-Human IgG, Fcγ fragment specific (Jackson Immuno Research Catalog #109-035-098) or Peroxid
    SARS-CoV2 LxC1-E7 human neutralizing mAb
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  11. Spike protein trimers were coated at 2 µg/mL and incubated with serially diluted antibodies. The bound antibodies were detected with Peroxidase AffiniPure Goat Anti-Human IgG, Fcγ fragment specific (Jackson Immuno Research catalog#109-035-098) or Peroxida
    SARS-CoV2 LxC1-G10 human neutralizing mAb
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  12. Spike protein trimers were coated at 2 µg/mL and incubated with serially diluted antibodies. The bound antibodies were detected with Peroxidase AffiniPure Goat Anti-Human IgG, Fcγ fragment specific (Jackson Immuno Research Catalog#109-035-098) or Peroxida
    SARS-CoV2 LxC1-G4 human neutralizing mAb
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  13. Concentration-response curves for binding of CoV2 spike protein Iota variant to human ACE2 in cell-free ELISA-type assays. Microtiter wells were coated with 100 uL of each spike trimer at 2 ug/mL in PBS at 4˚C overnight. The wells were washed with PBS and
    SARS-CoV2-2 Iota B.1.526 Variant Recombinant Spike Trimer His Tag
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  14. ST2/IL-33R (H2) rabbit mAb
    ST2/IL-33R (H2) rabbit mAb
    From $210.00
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  15. Immunoblot analysis of the indicated total and histone proteins in SY5Y NB cells, HCT116 and LOVO colon cancer cells, and 11 CR-CSphCs (left panel). Densitometry analysis of p53K382me1 protein levels compared with p53 total protein levels measured as rela
    p53-K382 monomethylated (R4BA1) Fab-His
    From $210.00
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