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3 protocols using sars cov 2 s1 his

1

Chemotaxis assay for SARS-CoV-2 proteins

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Recombinant human CXCL12β (3 nM), alone or in combination with purified recombinant proteins, was placed in the lower chamber of a 96-well ChemoTx System plate (Neuro Probe, nos. 101-3 and 101-5) in RPMI 1640 containing 1% FBS. As internal controls within each assay, medium or recombinant protein alone was used. PBMCs, MonoMac-1, and MOLT-4 cells (1.25 × 105) were placed on the upper compartment and separated from the lower chamber by a 3- or 5-μm pore size filter. The cells were incubated at 37°C for 3 hours in a humidified incubator with 5% CO2. The migrated cells in the lower chamber were stained with 5 μl of CellTiter 96 AQueous One Solution Cell Proliferation Assay (Promega, no. G3580) for 2 hours at 37°C with 5% CO2, measuring absorbance at 490 nm using a Synergy H1 plate reader (Bio-Tek).
The following recombinant proteins were used: SARS-CoV-2 S1-His (Sino Biological, no. 40591-V08B1), SARS-CoV-2 N-His (Sino Biological, no. 40588-V08B), SARS-CoV-2 N-His (Acro Biosystems, no. NUN-C5227), SARS-CoV-2 N-His (Ray Biotech, no. 230-30164), SARS-CoV-1 N-His (Acro Biosystems, no. NUN-S5229), and MERS-CoV N-His (Acro Biosystems, no. NUN-M52H5). SARS-CoV-2 N-His from Sino Biological (no. 40588-V08B) was used in all assays unless indicated.
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2

SARS-CoV-2 Protein-Driven Cellular Migration

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Recombinant human CXCL12β (3 nM), alone or in combination with purified recombinant proteins were placed in the lower chamber of a 96-well ChemoTx System plate (Neuro Probe # 101–3 and # 101–5) in RPMI 1640 1% FBS. As internal controls within each assay, medium or recombinant protein alone were used. PBMCs, MonoMac-1 and MOLT-4 cells (1.25 × 105) were placed on the upper compartment and separated from the lower chamber by a 3 or 5 μm pore size filter. The cells were incubated at 37° C for 3 h in a humidified incubator with 5% CO2. The migrated cells in the lower chamber were stained with 5 μl of CellTiter 96 AQueous One Solution Cell Proliferation Assay (Promega # G3580) for 2 h at 37° C with 5% CO2, measuring absorbance at 490 nm using a Synergy H1 plate reader (Bio-Tek).
The following recombinant proteins were used: SARS-CoV-2 S1-His (Sino Biological # 40591-V08B1), SARS-CoV-2 N-His (Sino Biological # 40588-V08B), SARS-CoV-2 N-His (Acro Biosystems # NUN-C5227), SARS-CoV-2 N-His (Ray Biotech # 230–30164), SARS-CoV-1 N-His (Acro Biosystems # NUN-S5229) and MERS-CoV N-His (Acro Biosystems # NUN-M52H5). SARS-CoV-2 N-His from Sino Biological (# 40588-V08B) was used in all assays unless indicated.
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3

Chemotaxis Assay for SARS-CoV-2 Proteins

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Recombinant human CXCL12β (3 nM), alone or in combination with purified recombinant proteins were placed in the lower chamber of a 96-well ChemoTx System plate (Neuro Probe # 101–3 and # 101–5) in RPMI 1640 1% FBS. As internal controls within each assay, medium or recombinant protein alone were used. PBMCs, MonoMac-1 and MOLT-4 cells (1.25 × 105) were placed on the upper compartment and separated from the lower chamber by a 3 or 5 µm pore size filter. The cells were incubated at 37° C for 3 h in a humidified incubator with 5% CO2. The migrated cells in the lower chamber were stained with 5 µl of CellTiter 96 AQueous One Solution Cell Proliferation Assay (Promega # G3580) for 2 h at 37° C with 5% CO2, measuring absorbance at 490 nm using a Synergy H1 plate reader (Bio-Tek).
The following recombinant proteins were used: SARS-CoV-2 S1-His (Sino Biological # 40591- V08B1), SARS-CoV-2 N-His (Sino Biological # 40588-V08B), SARS-CoV-2 N-His (Acro Biosystems # NUN-C5227), SARS-CoV-2 N-His (Ray Biotech # 230–30164), SARS-CoV-1 N-His (Acro Biosystems # NUN-S5229) and MERS-CoV N-His (Acro Biosystems # NUN-M52H5). SARS-CoV-2 N-His from Sino Biological (# 40588-V08B) was used in all assays unless indicated.
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