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Anti sars cov 2 nucleoprotein

Manufactured by Sino Biological

The anti-SARS-CoV-2 nucleoprotein is a laboratory reagent used for the detection and study of the SARS-CoV-2 virus. It is a recombinant protein that specifically binds to the nucleoprotein of the SARS-CoV-2 virus, which is a key component of the viral structure. This reagent can be used in various immunoassays and research applications to identify and quantify the presence of the SARS-CoV-2 virus.

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3 protocols using anti sars cov 2 nucleoprotein

1

Multimodal IHC for COVID-19 Markers

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Formalin (4%) fixed duodenum and colon tissue samples were embedded in paraffin, and a 4 μm section of each was obtained on a glass slide. These sections were deparaffinized and incubated with anti-HIV p24 (clone: Kal-1, Dako), anti–SARS-CoV-2 nucleoprotein (clone: 40143-T-62, Sino Biological) anti-ACE2 (clone: ab15348; Abcam), anti-TMPRSS2 (clone: ab109131; Abcam), and anti-EpCAM (clone: ab71916; Abcam) followed by a secondary antibody incubation using the Opal 4-color manual IHC (PerkinElmer) as instructed by the manufacturer. For Opal fluorophores (PerkinElmer), FITC (product number FP1487001KT; PerkinElmer) was used for EpCAM and p24, Texas red (product number FP1488001KT; PerkinElmer) for ACE2, and Cy5 (product number FP1497001KT; PerkinElmer) for TMPRSS2 and SARS-CoV-2 nucleoprotein signal generation. DAPI was used as the nuclear counterstain. The sections were mounted with the Fluorescence Mounting Medium (catalog number S302380-2; Agilent Technologies) and cover-slipped, and the edges were sealed with nail polish. The slides were stored at 2°C–8°C until images were acquired.
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2

Immunoblotting for SARS-CoV-2 Proteins

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Cell lysates were boiled in 2× Laemmli sample buffer containing 10% βME (Sigma, M3148). Cell lysates were analyzed by SDS-PAGE and then transferred onto polyvinylidene difluoride (PVDF) membranes (Millipore, IPFL10100). After blocking with 5% BSA in TBS buffer containing 0.05% Tween 20, the blot was sequentially probed with primary antibodies and the horseradish peroxidase (HRP)-conjugated secondary antibody. Protein bands were detected by SuperSignal West Pico Chemiluminescent substrate (Bio-Rad). The following antibodies were used: anti-ACE2 (Abcam, ab108209), anti-SARS-CoV-2 nucleoprotein (Sino Biological, 40588-T62), anti-p-hRIPK1 (Cell Signaling Technology, 65746), anti-RIPK1 (Cell Signaling Technology, 3493), anti-EGFR (Cell Signaling Technology, 4267), anti-NSP12(Cell Signaling Technology), anti-Flag (Sigma, F1804), anti-Myc (Sigma, C3956), anti-Strep tag II (Abcam, ab76949), anti-Actin (TransGen Biotech, HC201) and anti-Tubulin (TransGen Biotech, HC101).
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3

Placental SARS-CoV-2 Infection Analysis

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A total of 198 placentas delivered from SARS-CoV-2-positive pregnant women were submitted for conventional pathological analysis. Sampling was performed according to recommendations of the Amsterdam Consensus for placental sampling and report statements [10 (link)]. All placentas were immunohistochemically investigated for the presence of SARS-CoV-2 with the anti-SARS-CoV-2 nucleoprotein (Sino Biological, Wayne, PA) according to manufacturer's instructions. Immunohistochemically positive cases were further analyzed by in situ hybridization (ISH) with the RNAscope-ProbeV-nCoV2019-S (Advanced Cell Diagnostics, Hayward, CA). Thirty-three placentas were investigated for SARS-CoV-2 infection through retrotranscriptase PCR (RT-PCR). Fresh tissue samples and/or swabs were investigated by RT-PCR for SARS-CoV-2 with either the Allplex 2019-nCoV Assay (Seegene, Seoul, South Korea) or the Taqman 2019-nCoV Assay kit v.2 (ThermoFisher Scientific, Waltham, MA, US). For formaldehyde-fixed, paraffin embedded samples, RNA was obtained by High Pure FFPET extraction kit (Roche Diagnostics Gmbh) and further analyzed with CLART®COVID-19 (Genomica SAU) following the manufacturer's instructions. Clinical data were retrieved from the institutional records. Significance of association between qualitative variables was tested by Fisher's exact test with an α-risk of 0.05.
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