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COVID 19 Spike Coronavirus Pseudovirus

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SKU: MBS4342751
Brand: MyBioSource
UoM: Each
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LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
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LabMart Limited
Race Course st., Tabora No. 1, Accra, Greater Accra Region, Ghana
Not available
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MOQ : 1.0 Each
Estimated delivery Estimated delivery: 4-8 weeks
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The SARS-CoV-2 Pseudoviral Particles Spike are replication-deficient MLV pseudotyped viral particles bearing the SARS-CoV-2 spike (S) protein, available in both original D614 (Wuhan-Hu-1) and variant D614G spike forms. These pseudoviruses carry the firefly luciferase reporter gene, enabling quantitative measurement of spike-mediated viral entry into ACE2-expressing cells via luciferase activity.

They are optimized for use in viral entry assays, neutralizing antibody screening, and antiviral drug evaluation, providing a safe, non-replicative alternative to live SARS-CoV-2 for research use.

Key Features

  • Robust Signal – High signal-to-noise ratio for sensitive detection.
  • Reporter Gene – Firefly luciferase for luminescence-based quantification.
  • Safe & Non-Replicative – Pseudotyped MLV particles lacking replication capability.
  • High Particle Concentration – >1.0E+07 pseudoviral particles per mL.
  • HTS-Compatible – Amenable to 96-, 384-, and 1536-well assay formats.

Applications

  • SARS-CoV-2 Entry Assays – Measure spike-mediated entry via ACE2.
  • Neutralizing Antibody Screening – Evaluate antibody potency against spike variants.
  • Antiviral Drug Testing – Assess compounds that block spike-ACE2 interaction or entry.
  • Vaccine Research – Characterize immune response efficacy.

Related Products (Compatible Testing System)

  • Negative Control Pseudovirus – MLV-Luciferase without spike (Cat. No. MBS434280)
  • ACE2 Stable Cell Line – HEK293-ACE2 (Cat. No. MBS434276)
  • Firefly Luciferase Assay Kit – For luminescence readout 

Assay Principle

The spike protein binds to the human ACE2 receptor via its receptor-binding domain (RBD) and is activated by host proteases. In this pseudovirus system, successful cell entry results in luciferase expression, quantifiable with a luminescence plate reader.

Example Protocol Overview

  1. Seed ACE2-expressing target cells (e.g., HEK293-ACE2, Vero E6) in multiwell plates.
  2. Infect with pseudovirus (thawed quickly at RT, used immediately).
  3. Incubate for 48 hours (or as per protocol).
  4. Add luciferase assay working solution directly to wells.
  5. Read luminescence signal to quantify viral entry.

Neutralization Assay: Pre-incubate pseudovirus with serially diluted antibodies or inhibitors prior to cell infection to assess entry inhibition.

Technical Specifications

ParameterSpecification
Pseudovirus BackboneMLV (murine leukemia virus)
ReporterFirefly luciferase
Particle Concentration>1.0E+07 particles/mL
Volume5 mL (1 mL/tube)
FormatFrozen, shipped on dry ice
Storage–70°C; stable for 6 months
Assay Format Compatibility96-, 384-, 1536-well plates
Biosafety LevelBSL-2 recommended
Research UseFor research use only


The SARS-CoV-2 Pseudoviral Particles Spike offer a highly reliable, safe, and quantifiable platform for studying SARS-CoV-2 entry mechanisms, evaluating neutralizing antibodies, and screening antiviral agents. With luciferase-based detection and compatibility with high-throughput screening systems, these pseudoviruses are an essential research tool for COVID-19 virology and therapeutic development.

Application: Protein Assays & Analysis
Storage Temperature: –80°C
Product Type: Recombinant Protein
Product Brand: MyBioSource
Product Grade: Molecular Biology

The SARS-CoV-2 Pseudoviral Particles Spike are replication-deficient MLV pseudotyped viral particles bearing the SARS-CoV-2 spike (S) protein, available in both original D614 (Wuhan-Hu-1) and variant D614G spike forms. These pseudoviruses carry the firefly luciferase reporter gene, enabling quantitative measurement of spike-mediated viral entry into ACE2-expressing cells via luciferase activity.

They are optimized for use in viral entry assays, neutralizing antibody screening, and antiviral drug evaluation, providing a safe, non-replicative alternative to live SARS-CoV-2 for research use.

Key Features

  • Robust Signal – High signal-to-noise ratio for sensitive detection.
  • Reporter Gene – Firefly luciferase for luminescence-based quantification.
  • Safe & Non-Replicative – Pseudotyped MLV particles lacking replication capability.
  • High Particle Concentration – >1.0E+07 pseudoviral particles per mL.
  • HTS-Compatible – Amenable to 96-, 384-, and 1536-well assay formats.

Applications

  • SARS-CoV-2 Entry Assays – Measure spike-mediated entry via ACE2.
  • Neutralizing Antibody Screening – Evaluate antibody potency against spike variants.
  • Antiviral Drug Testing – Assess compounds that block spike-ACE2 interaction or entry.
  • Vaccine Research – Characterize immune response efficacy.

Related Products (Compatible Testing System)

  • Negative Control Pseudovirus – MLV-Luciferase without spike (Cat. No. MBS434280)
  • ACE2 Stable Cell Line – HEK293-ACE2 (Cat. No. MBS434276)
  • Firefly Luciferase Assay Kit – For luminescence readout 

Assay Principle

The spike protein binds to the human ACE2 receptor via its receptor-binding domain (RBD) and is activated by host proteases. In this pseudovirus system, successful cell entry results in luciferase expression, quantifiable with a luminescence plate reader.

Example Protocol Overview

  1. Seed ACE2-expressing target cells (e.g., HEK293-ACE2, Vero E6) in multiwell plates.
  2. Infect with pseudovirus (thawed quickly at RT, used immediately).
  3. Incubate for 48 hours (or as per protocol).
  4. Add luciferase assay working solution directly to wells.
  5. Read luminescence signal to quantify viral entry.

Neutralization Assay: Pre-incubate pseudovirus with serially diluted antibodies or inhibitors prior to cell infection to assess entry inhibition.

Technical Specifications

ParameterSpecification
Pseudovirus BackboneMLV (murine leukemia virus)
ReporterFirefly luciferase
Particle Concentration>1.0E+07 particles/mL
Volume5 mL (1 mL/tube)
FormatFrozen, shipped on dry ice
Storage–70°C; stable for 6 months
Assay Format Compatibility96-, 384-, 1536-well plates
Biosafety LevelBSL-2 recommended
Research UseFor research use only


The SARS-CoV-2 Pseudoviral Particles Spike offer a highly reliable, safe, and quantifiable platform for studying SARS-CoV-2 entry mechanisms, evaluating neutralizing antibodies, and screening antiviral agents. With luciferase-based detection and compatibility with high-throughput screening systems, these pseudoviruses are an essential research tool for COVID-19 virology and therapeutic development.

This will display Shipping & Return.

The SARS-CoV-2 Pseudoviral Particles Spike are replication-deficient MLV pseudotyped viral particles bearing the SARS-CoV-2 spike (S) protein, available in both original D614 (Wuhan-Hu-1) and variant D614G spike forms. These pseudoviruses carry the firefly luciferase reporter gene, enabling quantitative measurement of spike-mediated viral entry into ACE2-expressing cells via luciferase activity.

They are optimized for use in viral entry assays, neutralizing antibody screening, and antiviral drug evaluation, providing a safe, non-replicative alternative to live SARS-CoV-2 for research use.

Key Features

  • Robust Signal – High signal-to-noise ratio for sensitive detection.
  • Reporter Gene – Firefly luciferase for luminescence-based quantification.
  • Safe & Non-Replicative – Pseudotyped MLV particles lacking replication capability.
  • High Particle Concentration – >1.0E+07 pseudoviral particles per mL.
  • HTS-Compatible – Amenable to 96-, 384-, and 1536-well assay formats.

Applications

  • SARS-CoV-2 Entry Assays – Measure spike-mediated entry via ACE2.
  • Neutralizing Antibody Screening – Evaluate antibody potency against spike variants.
  • Antiviral Drug Testing – Assess compounds that block spike-ACE2 interaction or entry.
  • Vaccine Research – Characterize immune response efficacy.

Related Products (Compatible Testing System)

  • Negative Control Pseudovirus – MLV-Luciferase without spike (Cat. No. MBS434280)
  • ACE2 Stable Cell Line – HEK293-ACE2 (Cat. No. MBS434276)
  • Firefly Luciferase Assay Kit – For luminescence readout 

Assay Principle

The spike protein binds to the human ACE2 receptor via its receptor-binding domain (RBD) and is activated by host proteases. In this pseudovirus system, successful cell entry results in luciferase expression, quantifiable with a luminescence plate reader.

Example Protocol Overview

  1. Seed ACE2-expressing target cells (e.g., HEK293-ACE2, Vero E6) in multiwell plates.
  2. Infect with pseudovirus (thawed quickly at RT, used immediately).
  3. Incubate for 48 hours (or as per protocol).
  4. Add luciferase assay working solution directly to wells.
  5. Read luminescence signal to quantify viral entry.

Neutralization Assay: Pre-incubate pseudovirus with serially diluted antibodies or inhibitors prior to cell infection to assess entry inhibition.

Technical Specifications

ParameterSpecification
Pseudovirus BackboneMLV (murine leukemia virus)
ReporterFirefly luciferase
Particle Concentration>1.0E+07 particles/mL
Volume5 mL (1 mL/tube)
FormatFrozen, shipped on dry ice
Storage–70°C; stable for 6 months
Assay Format Compatibility96-, 384-, 1536-well plates
Biosafety LevelBSL-2 recommended
Research UseFor research use only


The SARS-CoV-2 Pseudoviral Particles Spike offer a highly reliable, safe, and quantifiable platform for studying SARS-CoV-2 entry mechanisms, evaluating neutralizing antibodies, and screening antiviral agents. With luciferase-based detection and compatibility with high-throughput screening systems, these pseudoviruses are an essential research tool for COVID-19 virology and therapeutic development.

This will display Shipping & Return.

Specifications

Pack Size 1 x 5 mL, 5 x 1mL