Membrane Protein (M) of SARS-CoV-2 / COVID-19
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Catalog Number:
SCV2-M-050P
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Membrane glycoprotein (aa 101-222), N-terminal His-tagged.
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Detailed Description
Keyword: coronavirus, SARS, SARS-Cov, SARS spike, SARS-CoV spike
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SCV2-M-050P
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Name
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Membrane Protein (M) (SARS-CoV-2/COVID-19)
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Description
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N-terminal His-tagged recombinant M protein (aa 101-222) (SARS-CoV-2) (GenBank No. QHD43419)
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Source
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Recombinant membrane protein of SARS-CoV-2 expressed and purified from E.coli
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Application
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Western blot standard, antibody ELISA, immunogen, etc.
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Purity
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> 95% (SDS-PAGE)
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Endotoxin
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><1 EU per µg of purified protein by LAL test
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Size
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50 µg
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For Downloading
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==>> DATA SHEET ==>> SAFETY DATA SHEET
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About SARS-CoV-2 Membrane (M) Protein
The Membrane (M) protein is the most abundant structural protein of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and plays a central role in viral assembly, morphogenesis, and particle formation. Unlike the Spike (S) protein, which mediates receptor binding and viral entry, the M protein functions primarily as a structural organizer of the viral envelope. The SARS-CoV-2 M protein is an integral membrane glycoprotein containing three transmembrane domains and is embedded within the viral envelope where it coordinates interactions with other structural proteins, including Spike (S), Envelope (E), and Nucleocapsid (N) proteins. These interactions are essential for efficient virion assembly and release of infectious viral particles.
The M protein is highly conserved among coronaviruses and contributes significantly to virion architecture and stability. During viral replication, M protein serves as a key scaffold that drives assembly of new virus particles within the endoplasmic reticulum-Golgi intermediate compartment (ERGIC). Through interactions with the N protein and viral RNA complexes, the M protein facilitates incorporation of the viral genome into newly formed virions. Because of its essential role in coronavirus assembly and its strong immunogenicity, the M protein has become an important target for studies of coronavirus biology, host immune responses, vaccine development, and antiviral therapeutic research.
eEnzyme's recombinant SARS-CoV-2 Membrane (M) Protein provides a valuable research reagent for investigations of coronavirus assembly, virus-host interactions, immune responses, structural biology, and antiviral drug discovery. The protein is suitable for antibody generation, epitope mapping, T-cell immune response studies, ELISA development, Western blot analysis, and characterization of coronavirus structural protein interactions. Researchers can utilize this recombinant antigen to investigate mechanisms of viral assembly, evaluate immune recognition, and support the development of next-generation vaccines, diagnostics, and antiviral therapeutics.
Applications of SARS-CoV-2 Membrane Protein
• Coronavirus assembly and morphogenesis studies • Virus-host interaction investigations • Antibody generation and characterization • T-cell immune response studies • Structural biology and protein interaction analysis • Vaccine antigen evaluation • ELISA, Western blot, and immunological assays • Antiviral therapeutic and diagnostic research
Biological Significance of the SARS-CoV-2 Membrane Protein
The Membrane protein serves as the central organizer of coronavirus particle assembly and is indispensable for the formation of infectious virions. Through interactions with Spike, Envelope, and Nucleocapsid proteins, M protein coordinates viral budding, envelope formation, and incorporation of viral genomic RNA into mature particles. In addition to its structural functions, the M protein has been shown to modulate host immune responses and influence viral pathogenesis. Because it is highly conserved across coronavirus strains and contributes to both viral replication and immune recognition, the M protein remains an important target for studies of coronavirus biology, vaccine design, antiviral development, and immune monitoring. Recombinant SARS-CoV-2 M protein continues to be widely used for investigating coronavirus assembly mechanisms, host-pathogen interactions, and adaptive immune responses to SARS-CoV-2 infection.
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