nucleocapsid n gene Search Results


90
Liferiver Bio Tech Corp nucleocapsid (n) gene sensitivity
Nucleocapsid (N) Gene Sensitivity, supplied by Liferiver Bio Tech Corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nucleocapsid (n) gene sensitivity/product/Liferiver Bio Tech Corp
Average 90 stars, based on 1 article reviews
nucleocapsid (n) gene sensitivity - by Bioz Stars, 2026-05
90/100 stars
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90
Biomatik expression plasmids encoding nucleocapsid (n) gene rsv or hmpv
HMPV infection is elevated in NECs from asthmatics with no associated defect in IFN production. a <t>RSV</t> or hMPV N gene copy number was quantified by RT-qPCR using total RNA extracted from NECs 24 h p.i. (MOI 3) and <t>control</t> <t>plasmids</t> for RSV and hMPV N gene and β-actin gene expression. b Secreted IFN-β was quantified by ALPHAlisa. c Secreted IFN-λ1 was quantified by ELISA. n = 10 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant for the viral load but not for the IFN response. * p < 0.05, ** p < 0.01 and **** p < 0.0001 show statistical significance.
Expression Plasmids Encoding Nucleocapsid (N) Gene Rsv Or Hmpv, supplied by Biomatik, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/expression plasmids encoding nucleocapsid (n) gene rsv or hmpv/product/Biomatik
Average 90 stars, based on 1 article reviews
expression plasmids encoding nucleocapsid (n) gene rsv or hmpv - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier

86
Bioedit Company nucleocapsid n gene
HMPV infection is elevated in NECs from asthmatics with no associated defect in IFN production. a <t>RSV</t> or hMPV N gene copy number was quantified by RT-qPCR using total RNA extracted from NECs 24 h p.i. (MOI 3) and <t>control</t> <t>plasmids</t> for RSV and hMPV N gene and β-actin gene expression. b Secreted IFN-β was quantified by ALPHAlisa. c Secreted IFN-λ1 was quantified by ELISA. n = 10 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant for the viral load but not for the IFN response. * p < 0.05, ** p < 0.01 and **** p < 0.0001 show statistical significance.
Nucleocapsid N Gene, supplied by Bioedit Company, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nucleocapsid n gene/product/Bioedit Company
Average 86 stars, based on 1 article reviews
nucleocapsid n gene - by Bioz Stars, 2026-05
86/100 stars
  Buy from Supplier

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HMPV infection is elevated in NECs from asthmatics with no associated defect in IFN production. a RSV or hMPV N gene copy number was quantified by RT-qPCR using total RNA extracted from NECs 24 h p.i. (MOI 3) and control plasmids for RSV and hMPV N gene and β-actin gene expression. b Secreted IFN-β was quantified by ALPHAlisa. c Secreted IFN-λ1 was quantified by ELISA. n = 10 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant for the viral load but not for the IFN response. * p < 0.05, ** p < 0.01 and **** p < 0.0001 show statistical significance.

Journal: Journal of Innate Immunity

Article Title: Human Metapneumovirus Impairs Apoptosis of Nasal Epithelial Cells in Asthma via HSP70

doi: 10.1159/000449101

Figure Lengend Snippet: HMPV infection is elevated in NECs from asthmatics with no associated defect in IFN production. a RSV or hMPV N gene copy number was quantified by RT-qPCR using total RNA extracted from NECs 24 h p.i. (MOI 3) and control plasmids for RSV and hMPV N gene and β-actin gene expression. b Secreted IFN-β was quantified by ALPHAlisa. c Secreted IFN-λ1 was quantified by ELISA. n = 10 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant for the viral load but not for the IFN response. * p < 0.05, ** p < 0.01 and **** p < 0.0001 show statistical significance.

Article Snippet: RSV and hMPV intracellular RNA was quantified using SYBR green dye (QIAGEN), specific primers (online suppl. table S1 ; for all online suppl. material, see www.karger.com/doi/10.1159/000449101 ) and standard curves were generated using 10-fold serial dilutions of expression plasmids encoding the nucleocapsid (N) gene of RSV or hMPV (Biomatik).

Techniques: Infection, Quantitative RT-PCR, Expressing, Enzyme-linked Immunosorbent Assay

Apoptosis in response to hMPV is reduced in NECs from asthmatics. a Representative Annexin-V/7-AAD staining of NECs infected with hMPV or RSV at a MOI of 3 at 24 h p.i. b Quantification of the proportion of Annexin-V+ NECs at 24 h p.i. when normalized with Annexin-V-positive uninfected cells. n = 5 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant. Statistical significance between asthmatic and non-asthmatic NECs is indicated by ** p < 0.01 and **** p < 0.0001.

Journal: Journal of Innate Immunity

Article Title: Human Metapneumovirus Impairs Apoptosis of Nasal Epithelial Cells in Asthma via HSP70

doi: 10.1159/000449101

Figure Lengend Snippet: Apoptosis in response to hMPV is reduced in NECs from asthmatics. a Representative Annexin-V/7-AAD staining of NECs infected with hMPV or RSV at a MOI of 3 at 24 h p.i. b Quantification of the proportion of Annexin-V+ NECs at 24 h p.i. when normalized with Annexin-V-positive uninfected cells. n = 5 for both asthmatics and non-asthmatics. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and virus was significant. Statistical significance between asthmatic and non-asthmatic NECs is indicated by ** p < 0.01 and **** p < 0.0001.

Article Snippet: RSV and hMPV intracellular RNA was quantified using SYBR green dye (QIAGEN), specific primers (online suppl. table S1 ; for all online suppl. material, see www.karger.com/doi/10.1159/000449101 ) and standard curves were generated using 10-fold serial dilutions of expression plasmids encoding the nucleocapsid (N) gene of RSV or hMPV (Biomatik).

Techniques: Staining, Infection

Caspase-3/7 and caspase-9 activity in NECs from asthmatic subjects is reduced in response to hMPV. Caspase-3/7 (a, b) and caspase-9 (c, d) activation was quantified by luminescence detection at the indicated time points within 24 h following hMPV or RSV infection (MOI 3). n = 5 for both asthmatics and non-asthmatics; median ± range. Caspase-3/7 (e) and caspase-9 (f)activation were quantified at 4, 8 and 12 h after treatment with 10 µM AT-101. n = 5 for both asthmatics and non-asthmatics; median ± range. A GEE approach was used to compare groups and the interaction between disease status and time following hMPV infection was significant. Statistical significance between asthmatic and non-asthmatic NECs is indicated by ** p < 0.01 and **** p < 0.0001. Statistical significance between infected (or treated) and uninfected (or untreated) NECs is indicated by † p < 0.05, †† p < 0.01, ††† p < 0.001 and †††† p < 0.0001.

Journal: Journal of Innate Immunity

Article Title: Human Metapneumovirus Impairs Apoptosis of Nasal Epithelial Cells in Asthma via HSP70

doi: 10.1159/000449101

Figure Lengend Snippet: Caspase-3/7 and caspase-9 activity in NECs from asthmatic subjects is reduced in response to hMPV. Caspase-3/7 (a, b) and caspase-9 (c, d) activation was quantified by luminescence detection at the indicated time points within 24 h following hMPV or RSV infection (MOI 3). n = 5 for both asthmatics and non-asthmatics; median ± range. Caspase-3/7 (e) and caspase-9 (f)activation were quantified at 4, 8 and 12 h after treatment with 10 µM AT-101. n = 5 for both asthmatics and non-asthmatics; median ± range. A GEE approach was used to compare groups and the interaction between disease status and time following hMPV infection was significant. Statistical significance between asthmatic and non-asthmatic NECs is indicated by ** p < 0.01 and **** p < 0.0001. Statistical significance between infected (or treated) and uninfected (or untreated) NECs is indicated by † p < 0.05, †† p < 0.01, ††† p < 0.001 and †††† p < 0.0001.

Article Snippet: RSV and hMPV intracellular RNA was quantified using SYBR green dye (QIAGEN), specific primers (online suppl. table S1 ; for all online suppl. material, see www.karger.com/doi/10.1159/000449101 ) and standard curves were generated using 10-fold serial dilutions of expression plasmids encoding the nucleocapsid (N) gene of RSV or hMPV (Biomatik).

Techniques: Activity Assay, Activation Assay, Infection

HMPV induced the expression of ER stress and unfolded protein response markers in NECs from both asthmatic and non-asthmatic subjects. Grp78 (a), sXBP1 (b), CHOP (c), GADD34 (d), PUMA (e) and NOXA (f) mRNA expression in NECs at 8, 12 and 24 h following infection with hMPV or RSV (Grp78 and sXBP1 only; MOI of 3). RT-qPCR was performed using total cellular RNA. Fold induction was calculated using 2−ΔΔCt normalized to the expression of β-actin gene. n = 5 for both asthmatic and non-asthmatic subjects. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and time (hMPV time course) or between disease status and virus (hMPV vs. RSV at 24 h p.i.) was not significant. * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001 indicate statistical significance.

Journal: Journal of Innate Immunity

Article Title: Human Metapneumovirus Impairs Apoptosis of Nasal Epithelial Cells in Asthma via HSP70

doi: 10.1159/000449101

Figure Lengend Snippet: HMPV induced the expression of ER stress and unfolded protein response markers in NECs from both asthmatic and non-asthmatic subjects. Grp78 (a), sXBP1 (b), CHOP (c), GADD34 (d), PUMA (e) and NOXA (f) mRNA expression in NECs at 8, 12 and 24 h following infection with hMPV or RSV (Grp78 and sXBP1 only; MOI of 3). RT-qPCR was performed using total cellular RNA. Fold induction was calculated using 2−ΔΔCt normalized to the expression of β-actin gene. n = 5 for both asthmatic and non-asthmatic subjects. The bottom and top of the box plots represent the 5th and 95th percentiles, the bar represents the median and the whiskers represent minimum and maximum. A GEE approach was used to compare groups and the interaction between disease status and time (hMPV time course) or between disease status and virus (hMPV vs. RSV at 24 h p.i.) was not significant. * p < 0.05, ** p < 0.01, *** p < 0.001 and **** p < 0.0001 indicate statistical significance.

Article Snippet: RSV and hMPV intracellular RNA was quantified using SYBR green dye (QIAGEN), specific primers (online suppl. table S1 ; for all online suppl. material, see www.karger.com/doi/10.1159/000449101 ) and standard curves were generated using 10-fold serial dilutions of expression plasmids encoding the nucleocapsid (N) gene of RSV or hMPV (Biomatik).

Techniques: Expressing, Infection, Quantitative RT-PCR