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Comments

(S2N-C52H5) SARS-CoV-2 Spike S2 Protein, His Tag

Supplied by ACROBiosystems, cited in 15 publications. Applications used include FC/FACS, ELISA, and SPR.

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Supplier info
15 citations

General Information

Supplier
ACROBiosystems
Purified
No
Bioactive
No
Nature
Recombinant
Protein Name
Spike glycoprotein
UniProt ID
P0DTC2 - SPIKE_SARS2
Species
Severe acute respiratory syndrome coronavirus 2 (2019-nCoV)
Gene
S

Supplier provided information

Applications

None provided

Reactivity

  • SARS-CoV-2

Additional product information

Synonyms

Spike,S2 protein,Spike glycoprotein Subunit2,S glycoprotein Subunit2,Spike protein S2,COVID-19

Protein Names

Spike glycoprotein, E2, Peplomer protein, SPIKE_SARS2

UniProt Code History

P0DTC2

Gene

S, spike glycoprotein


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0 images
15 citations

found in the literature

Applications
  • FC/FACS
  • ELISA
  • SPR
Reactivity
  • None Available
Dilutions
  • None Available

Published images

We have not yet identified suitable images that show this product being used, more are being added all the time.

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Ultrapotent SARS coronavirus-neutralizing single-domain antibodies that clamp the spike at its base.

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In Nature Communications on 30 May 2025 by De Cae, S., Van Molle, I., et al.

MENSA, a Media Enriched with Newly Synthesized Antibodies, to Identify SARS-CoV-2 Persistence and Latent Viral Reactivation in Long-COVID

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Preprint on Research Square on 1 August 2024 by Lee, F., Haddad, N. S., et al.

MENSA, a Media Enriched with Newly Synthesized Antibodies, to Identify SARS-CoV-2 Persistence and Latent Viral Reactivation in Long-COVID

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Preprint on MedRxiv : the Preprint Server for Health Sciences on 7 July 2024 by Haddad, N. S., Morrison-Porter, A., et al.

Ultrapotent SARS coronavirus-neutralizing single-domain antibodies that bind a conserved membrane proximal epitope of the spike

Preprint on BioRxiv : the Preprint Server for Biology on 10 March 2023 by De Cae, S., Van Molle, I., et al.

The BNT162b2 mRNA SARS-CoV-2 vaccine induces transient afucosylated IgG1 in naive but not in antigen-experienced vaccinees.

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In EBioMedicine on 1 January 2023 by Van Coillie, J., Pongrácz, T., et al.

Dysregulated naive B cells and de novo autoreactivity in severe COVID-19.

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In Nature on 1 November 2022 by Woodruff, M. C., Ramonell, R. P., et al.

SARS-CoV-2 infections elicit higher levels of original antigenic sin antibodies compared with SARS-CoV-2 mRNA vaccinations.

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In Cell Reports on 18 October 2022 by Anderson, E. M., Li, S. H., et al.

Both COVID-19 infection and vaccination induce high-affinity cross-clade responses to SARS-CoV-2 variants.

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In IScience on 19 August 2022 by Emmenegger, M., Fiedler, S., et al.

Evidence for investigating GSK-3 inhibitors as potential therapeutics for severe COVID-19.

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In Biochemical and Biophysical Research Communications on 21 May 2022 by Ghazanfari, D., Courreges, M. C., et al.

Microfluidic Antibody Affinity Profiling Reveals the Role of Memory Reactivation and Cross-Reactivity in the Defense Against SARS-CoV-2.

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In ACS Infectious Diseases on 8 April 2022 by Denninger, V., Xu, C. K., et al.

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  • +1 800-810-0816
  • 1 Innovation Way, Newark, DE 19711, USA

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