With the outbreak of COVID-19 in the Chinese city of Wuhan, infection prevention and control has become critical. To support SARS-CoV-2 research we put together a large collection of antibodies against different SARS-CoV-2 targets. Products for spike protein, membrane protein, envelope protein, nucleocapsid protein and non structural proteins are available. These antibodies can be used for detection of the virus in a variety of applications including IHC, ELISA, WB, IF staining. We also offer a set of neutralizing antibodies based on clone CR3022. Discover our SARS-CoV-2 antibody portfolio below.
NEW: Discover our proteins for variant B.1.1.529!
NEW: Discover our proteins for variant B.1.1.529!
We support you with a range of recombinant spike B.1.1.529 / Omicron proteins. Conjugates e.g. His-tag, Avi-tag, rho-1D4 tag etc.
We support you with a range of recombinant spike B.1.1.529 / Omicron proteins.
Conjugates e.g. His-tag, Avi-tag, rho-1D4 tag etc.
The SARS-CoV-2 spike protein protrudes from the envelope of the virion and plays a pivotal role in the receptor host selectivity and cellular attachment. Strong scientific evidence showed that SARS and SARS-CoV-2 spike proteins interact with angiotensin-converting enzyme 2 (ACE2).(1)
The nucleocapsid (N) protein is an important antigen for coronavirus, which participate in RNA package and virus particle release. After infection, the N protein enters the host cell together with the viral RNA to facilitate its replication and process the virus particle assembly and release. SARS-CoV-2 N protein contains two distinct RNA-binding domains (NTD and CTD) linked by a poorly structured linkage region containing a serine/arginine-rich (SR-rich) domain. (2) Below you will find a selection of our CoV SARS-CoV-2 nucleocapsid protein antibodies.
Rabbit Monoclonal SARS-CoV-2 N-Protein Antibodies
Rabbit monoclonals offer an improved immune response to small epitopes and a better response to mouse antigens. They give a better reaction to antigens than those from rodents such as mice. Because of their advantages rabbit monoclonal antibodies are becoming more preferred in research and clinical applications.
The E protein is the smallest of the major structural proteins of SARS-CoV-2 and participates in viral assembly and budding. During the replication cycle, E is abundantly expressed inside the infected cell, but only a small portion is incorporated into the virion envelope. The majority of the protein is localised at the site of intracellular trafficking.(3) We currently offer two E-protein antibodies
SARS-CoV-2 E-protein antibody ABIN1031551
SARS-CoV-2 E-protein antibody ABIN6952904
Below you will find the available SARS-CoV-2 Envelope protein antibodies. Click on the links to see more details.
The coronavirus membrane (M) protein is the key player in virion assembly. One of its functions is to mediate the incorporation of the spikes into the viral envelope. When expressed alone, it accumulates in the Golgi complex in homomultimeric complexes. However, in combination with the E protein, virus-like particles (VLPs) similar to authentic virions in size and shape are assembled, demonstrating that the M and E proteins are the minimal requirements for envelope formation.(4) We currently offer one
SARS-CoV-2 M-protein antibody
(rabbit polyclonal for ELISA, WB).
Below you will find a selection of our SARS-CoV-2 and SARS-CoV membrane protein antibodies. Click on the links to see more details.
We help you with finding the right product for your research.
We offer reliable antibodies, kits, proteins, lysates for COVID-19 research.
Contact us via email or phone: (877) 302 8632 (US) or +49 241 95 163 153 (International)
Florindo, H.F., Kleiner, R., Vaskovich-Koubi, D. et al. Immune-mediated approaches against COVID-19. Nat. Nanotechnol. 15, 630–645 (2020). https://doi.org/10.1038/s41565-020-0732-3
Kandimalla, R., John, A., Abburi, C. et al. Current Status of Multiple Drug Molecules, and Vaccines: An Update in SARS-CoV-2 Therapeutics. Mol Neurobiol 57, 4106–4116 (2020). https://doi.org/10.1007/s12035-020-02022-0
Ortega J. T., Serrano M. L., Pujol F. H., Rangel H. R. Role of changes in SARS-CoV-2 spike protein in the interaction with the human ACE2 receptor: An in silico analysis. EXCLI J. 2020; 19: 410–417. PMID: 32210742.
Thao, T. T. N. et al. Rapid reconstruction of SARS-CoV-2 using a synthetic genomics platform. Nature https://doi.org/10.1038/s41586-020-2294-9 (2020).
Weihong Zeng, Guangfeng Liu, Huan Ma, Dan Zhao et al. Biochemical characterization of SARS-CoV-2 nucleocapsid protein. Biochem Biophys Res Commun. 2020 Jun 30; 527(3): 618–623. PMID: 32416961
de Haan CA, Smeets M, Vernooij F, Vennema H, Rottier PJ. Mapping of the coronavirus membrane protein domains involved in interaction with the spike protein. J Virol. 1999 Sep;73(9):7441-52. PMID: 10438834; PMCID: PMC104271.
Roujian Lu, Xiang Zhao, Juan Li, Peihua Niu, Bo Yang, Honglong Wu et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding. January 30, 2020.