viral strains hcov 229e Search Results


96
ATCC human coronavirus 229e
Analytical specificity evaluation results of the Kaira assay.
Human Coronavirus 229e, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sino Biological rabbit anti 229e nucleocapsid protein antibody
Analytical specificity evaluation results of the Kaira assay.
Rabbit Anti 229e Nucleocapsid Protein Antibody, supplied by Sino Biological, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
ATCC hcov 229e
Analytical specificity evaluation results of the Kaira assay.
Hcov 229e, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC human coronavirus oc43
The pan-CoV assay was evaluated against a panel of known coronaviruses and other unrelated human respiratory virus pathogens.
Human Coronavirus Oc43, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
ATCC hcov 229e rna levels
Detection of a 548-nucleotide deletion in a <t>HCoV</t> <t>229E</t> strain associated with myeloablation. a Depiction of the case history surrounding myeloablation and coronavirus infection. A woman in her 40s with AML was found to be infected with a <t>HCoV</t> <t>229E</t> just before her HCT. Due to the patient’s advanced disease, the decision was made to continue with the transplant. Four successive HCoV-positive nasal swab specimens were available from the patient; two from before treatment with myeloablative cyclophosphamide and total body irradiation and two from after. All days are reported relative to HCT. b Coverage plots of mNGS reads mapped to the reference genome for HCoV 229E (NC_002645) of three samples from the patient revealed the generation of a 548-nucleotide deletion in the ORF4a/4b gene. In addition to deleting 83% of the coding region from ORF4a/4b, the deletion resulted in a frame shift that resulted in a premature stop codon 10 amino acids before the reference genome stop codon. Primer binding sites are denoted in blue for confirmatory junction RT-PCR. c Confirmatory junction RT-PCR of the four available HCoV-positive nasal swabs revealed the absence of the deletion before myeloablation and the presence of the deletion in specimens taken after myeloablation. NTC , no template control
Hcov 229e Rna Levels, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Sino Biological hcov 229e nucleocapsid protein
Detection of a 548-nucleotide deletion in a <t>HCoV</t> <t>229E</t> strain associated with myeloablation. a Depiction of the case history surrounding myeloablation and coronavirus infection. A woman in her 40s with AML was found to be infected with a <t>HCoV</t> <t>229E</t> just before her HCT. Due to the patient’s advanced disease, the decision was made to continue with the transplant. Four successive HCoV-positive nasal swab specimens were available from the patient; two from before treatment with myeloablative cyclophosphamide and total body irradiation and two from after. All days are reported relative to HCT. b Coverage plots of mNGS reads mapped to the reference genome for HCoV 229E (NC_002645) of three samples from the patient revealed the generation of a 548-nucleotide deletion in the ORF4a/4b gene. In addition to deleting 83% of the coding region from ORF4a/4b, the deletion resulted in a frame shift that resulted in a premature stop codon 10 amino acids before the reference genome stop codon. Primer binding sites are denoted in blue for confirmatory junction RT-PCR. c Confirmatory junction RT-PCR of the four available HCoV-positive nasal swabs revealed the absence of the deletion before myeloablation and the presence of the deletion in specimens taken after myeloablation. NTC , no template control
Hcov 229e Nucleocapsid Protein, supplied by Sino Biological, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
ZeptoMetrix corporation hcov oc43
Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs <t>(HCoV-OC43,</t> HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.
Hcov Oc43, supplied by ZeptoMetrix corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sino Biological rabbit polyclonal antibody against hcov 229e nucleocapsid protein
Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs <t>(HCoV-OC43,</t> HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.
Rabbit Polyclonal Antibody Against Hcov 229e Nucleocapsid Protein, supplied by Sino Biological, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Qiagen qiaamp viral rna mini kit
Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs <t>(HCoV-OC43,</t> HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.
Qiaamp Viral Rna Mini Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
ATCC strains murine norovirus 1 mnv 1
Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs <t>(HCoV-OC43,</t> HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.
Strains Murine Norovirus 1 Mnv 1, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Analytical specificity evaluation results of the Kaira assay.

Journal: PLOS ONE

Article Title: Evaluation of the Kaira COVID-19/Flu/RSV Detection Kit for detection of SARS-CoV-2, influenza A/B, and respiratory syncytial virus: A comparative study with the PowerChek SARS-CoV-2, influenza A&B, RSV Multiplex Real-time PCR Kit

doi: 10.1371/journal.pone.0278530

Figure Lengend Snippet: Analytical specificity evaluation results of the Kaira assay.

Article Snippet: Human coronavirus 229E , ATCC (VR-740D) , Negative.

Techniques: Virus

The pan-CoV assay was evaluated against a panel of known coronaviruses and other unrelated human respiratory virus pathogens.

Journal: Journal of Clinical Virology

Article Title: A RT-PCR assay for the detection of coronaviruses from four genera

doi: 10.1016/j.jcv.2020.104391

Figure Lengend Snippet: The pan-CoV assay was evaluated against a panel of known coronaviruses and other unrelated human respiratory virus pathogens.

Article Snippet: Human coronavirus OC43 , β CoV , Lab strain , Betacoronavirus 1; ATCC.

Techniques: Virus, Plasmid Preparation, Derivative Assay

Detection of a 548-nucleotide deletion in a HCoV 229E strain associated with myeloablation. a Depiction of the case history surrounding myeloablation and coronavirus infection. A woman in her 40s with AML was found to be infected with a HCoV 229E just before her HCT. Due to the patient’s advanced disease, the decision was made to continue with the transplant. Four successive HCoV-positive nasal swab specimens were available from the patient; two from before treatment with myeloablative cyclophosphamide and total body irradiation and two from after. All days are reported relative to HCT. b Coverage plots of mNGS reads mapped to the reference genome for HCoV 229E (NC_002645) of three samples from the patient revealed the generation of a 548-nucleotide deletion in the ORF4a/4b gene. In addition to deleting 83% of the coding region from ORF4a/4b, the deletion resulted in a frame shift that resulted in a premature stop codon 10 amino acids before the reference genome stop codon. Primer binding sites are denoted in blue for confirmatory junction RT-PCR. c Confirmatory junction RT-PCR of the four available HCoV-positive nasal swabs revealed the absence of the deletion before myeloablation and the presence of the deletion in specimens taken after myeloablation. NTC , no template control

Journal: NPJ Genomic Medicine

Article Title: Myeloablation-associated deletion of ORF4 in a human coronavirus 229E infection

doi: 10.1038/s41525-017-0033-4

Figure Lengend Snippet: Detection of a 548-nucleotide deletion in a HCoV 229E strain associated with myeloablation. a Depiction of the case history surrounding myeloablation and coronavirus infection. A woman in her 40s with AML was found to be infected with a HCoV 229E just before her HCT. Due to the patient’s advanced disease, the decision was made to continue with the transplant. Four successive HCoV-positive nasal swab specimens were available from the patient; two from before treatment with myeloablative cyclophosphamide and total body irradiation and two from after. All days are reported relative to HCT. b Coverage plots of mNGS reads mapped to the reference genome for HCoV 229E (NC_002645) of three samples from the patient revealed the generation of a 548-nucleotide deletion in the ORF4a/4b gene. In addition to deleting 83% of the coding region from ORF4a/4b, the deletion resulted in a frame shift that resulted in a premature stop codon 10 amino acids before the reference genome stop codon. Primer binding sites are denoted in blue for confirmatory junction RT-PCR. c Confirmatory junction RT-PCR of the four available HCoV-positive nasal swabs revealed the absence of the deletion before myeloablation and the presence of the deletion in specimens taken after myeloablation. NTC , no template control

Article Snippet: No CPE was visualized for any of the patient’s four clinical samples and HCoV 229E RNA levels in the culture supernatant were undetectable by qRT-PCR after inoculation, while viral growth was apparent in the positive control HCoV 229E ATCC type strain (Figure ).

Techniques: Infection, Irradiation, Binding Assay, Reverse Transcription Polymerase Chain Reaction, Control

Specimens sequenced in this study

Journal: NPJ Genomic Medicine

Article Title: Myeloablation-associated deletion of ORF4 in a human coronavirus 229E infection

doi: 10.1038/s41525-017-0033-4

Figure Lengend Snippet: Specimens sequenced in this study

Article Snippet: No CPE was visualized for any of the patient’s four clinical samples and HCoV 229E RNA levels in the culture supernatant were undetectable by qRT-PCR after inoculation, while viral growth was apparent in the positive control HCoV 229E ATCC type strain (Figure ).

Techniques:

Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs (HCoV-OC43, HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: Genome-wide CRISPR Screens Identify Host Factors Required for SARS-CoV-2 Infection (A) Genome-wide CRISPR screening workflow. Cas9-expressing Huh-7.5 cells are transduced with the Brunello genome-wide CRISPR library, selected with puromycin, and infected with SARS-CoV-2 or one of three seasonal CoVs (HCoV-OC43, HCoV-NL63, or HCoV-229E). Surviving cells and mock controls are then harvested, and sgRNA abundance is determined using next-generation sequencing. (B) Bubble plot of data from SARS-CoV-2 screens at 37°C. Red lines denote z = ±2. (C) Bubble plot of data from SARS-CoV-2 screens at 33°C. Red lines denote z = ±2. (D) Scatterplot comparing Z scores from (B) and (C) for SARS-CoV-2 screens at 37°C and 33°C, respectively. (E) Subset of significantly enriched genes from SARS-CoV-2 screens at 37°C and 33°C.

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Genome Wide, CRISPR, Infection, Expressing, Transduction, Next-Generation Sequencing

Analysis of Established and Putative CoV Host Factors and Gene-wise Fitness Scores for SARS-CoV-2 and 3 Seasonal CoVs, Related to and (A) Heatmap of z-scores for known and putative coronavirus host factors. (B-D) Genewise fitness beta scatterplots comparing SARS-CoV-2 at 37°C versus mock (B), SARS-CoV-2 at 33°C versus mock (C), and SARS-CoV-2 at 33°C versus SARS-CoV-2 at 37°C (D). Non-targeting controls and essential control genes are highlighted in blue and red, respectively. (E) HCoV-OC43 versus mock infected. (F) HCoV-NL63 versus mock infected. (G) HCoV-229E versus mock infected.

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: Analysis of Established and Putative CoV Host Factors and Gene-wise Fitness Scores for SARS-CoV-2 and 3 Seasonal CoVs, Related to and (A) Heatmap of z-scores for known and putative coronavirus host factors. (B-D) Genewise fitness beta scatterplots comparing SARS-CoV-2 at 37°C versus mock (B), SARS-CoV-2 at 33°C versus mock (C), and SARS-CoV-2 at 33°C versus SARS-CoV-2 at 37°C (D). Non-targeting controls and essential control genes are highlighted in blue and red, respectively. (E) HCoV-OC43 versus mock infected. (F) HCoV-NL63 versus mock infected. (G) HCoV-229E versus mock infected.

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Control, Infection

Parallel Genome-wide CRISPR Screening against Multiple HCoVs Uncovers Host Factors and Pathways with Pan-CoV and Virus-Specific Functional Roles (A) Bubble plot of data from HCoV-OC43 screens at 33°C. Red lines denote z = ±2. (B) Bubble plot of data from HCoV-NL63 screens at 33°C. Red lines denote z = ±2. (C) Bubble plot of data from HCoV-229E screens at 33°C. Red lines denote z = ±2. (D) UpSet plot showing enriched hits overlapping in screens across all four viruses. Select genes for enriched sgRNAs are indicated.

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: Parallel Genome-wide CRISPR Screening against Multiple HCoVs Uncovers Host Factors and Pathways with Pan-CoV and Virus-Specific Functional Roles (A) Bubble plot of data from HCoV-OC43 screens at 33°C. Red lines denote z = ±2. (B) Bubble plot of data from HCoV-NL63 screens at 33°C. Red lines denote z = ±2. (C) Bubble plot of data from HCoV-229E screens at 33°C. Red lines denote z = ±2. (D) UpSet plot showing enriched hits overlapping in screens across all four viruses. Select genes for enriched sgRNAs are indicated.

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Genome Wide, CRISPR, Virus, Functional Assay

Expanded CoV-Specific Networks, Related to <xref ref-type=Figure 3 (A–D) Network diagram of all coronavirus screen hits and the next 100 adjacent interactors, shown in gray. Broad functional categories of highly interconnected gene neighborhoods are indicated. Diagrams are for SARS-CoV-2 (A), HCoV-OC43 (B), HCoV-NL63 (C) and HCoV-229E (D). " width="100%" height="100%">

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: Expanded CoV-Specific Networks, Related to Figure 3 (A–D) Network diagram of all coronavirus screen hits and the next 100 adjacent interactors, shown in gray. Broad functional categories of highly interconnected gene neighborhoods are indicated. Diagrams are for SARS-CoV-2 (A), HCoV-OC43 (B), HCoV-NL63 (C) and HCoV-229E (D).

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Functional Assay

Validation of High-Confidence Coronaviridae Host Factors (A) Candidate validation in Huh-7.5 cells with SARS-CoV-2 infection at 33°C. (B) Candidate validation in Huh-7.5 cells with HCoV-OC43 infection at 33°C. (C) Candidate validation in Huh-7.5 cells with HCoV-NL63 at 33°C. (D) Candidate validation in Huh-7.5 cells with HCoV-229E at 37°C. (E) Heatmap representation of data from (A)–(D). The SARS-CoV-2 and HCoV-NL-63 receptor ( ACE2 ) and the HCoV-229E receptor ( ANPEP ) are shown separately.

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: Validation of High-Confidence Coronaviridae Host Factors (A) Candidate validation in Huh-7.5 cells with SARS-CoV-2 infection at 33°C. (B) Candidate validation in Huh-7.5 cells with HCoV-OC43 infection at 33°C. (C) Candidate validation in Huh-7.5 cells with HCoV-NL63 at 33°C. (D) Candidate validation in Huh-7.5 cells with HCoV-229E at 37°C. (E) Heatmap representation of data from (A)–(D). The SARS-CoV-2 and HCoV-NL-63 receptor ( ACE2 ) and the HCoV-229E receptor ( ANPEP ) are shown separately.

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Infection

A Majority of Functional CoV Host Factors Are Expressed in the Airway, Related to , , and (A–D) scRNaseq expression dotplot diagrams from select cells in the airway of the average expression and the percent of cells expressing coronavirus host factors for SARS-CoV-2 (A), HCoV-OC43 (B), HCoV-NL63 (C) and HCoV-229E (D). Rows for each diagram are ordered top to bottom from highest to lowest z-score. Data are from <xref ref-type=Chua et al. (2020) . " width="100%" height="100%">

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet: A Majority of Functional CoV Host Factors Are Expressed in the Airway, Related to , , and (A–D) scRNaseq expression dotplot diagrams from select cells in the airway of the average expression and the percent of cells expressing coronavirus host factors for SARS-CoV-2 (A), HCoV-OC43 (B), HCoV-NL63 (C) and HCoV-229E (D). Rows for each diagram are ordered top to bottom from highest to lowest z-score. Data are from Chua et al. (2020) .

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Functional Assay, Expressing

Journal: Cell

Article Title: Genome-Scale Identification of SARS-CoV-2 and Pan-coronavirus Host Factor Networks

doi: 10.1016/j.cell.2020.12.006

Figure Lengend Snippet:

Article Snippet: HCoV-OC43 , ZeptoMetrix , Cat#0810024CF.

Techniques: Virus, Recombinant, SYBR Green Assay, Luciferase, DNA Purification, Plasmid Preparation, CRISPR, Software, Genome Wide, Knock-Out, Inverted Microscopy