monolisa hbsag ultra enzyme-linked immunosorbent assay (elisa) kit Search Results


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monolisa hcv-ab-ag ultra assay  (Bio-Rad)
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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ortho hcv 3.0 elisa monolisa anti-hcv  (Sanofi)
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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elisa monolisa hbsag ultra  (Immunodiagnostic Systems)
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Characteristics of studies included in the systematic review on <t> HCV antibody </t> detection from DBS compared to venous blood sampling
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hbsag elisa plates  (Bio-Rad)
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Calcitriol inhibits HBV core promoter transcripts, HBV secretory proteins, but not HBV virion secretion. The 1.3×-HBV genome construct was transfected in HepG2 and Huh7 cells, whereas HepG2.2.15 stably expresses HBV genome. In the HBV infection model, HBV particles derived from HepG2.2.15 cells were used to infect HepG2-NTCP cells as described in the section. Vehicle control (without calcitriol) or 10 nM calcitriol was added immediately after transfection or infection, and samples were processed as described in the section. RNA isolation and quantitation by quantitative PCR (qPCR) shows that ( A ) HBV pcRNA and ( B ) HBV pgRNA are suppressed in the presence of calcitriol. Quantitation of HBV secretory proteins by <t>ELISA</t> demonstrates that calcitriol negatively regulates ( C ) HBeAg and ( D ) <t>HBsAg.</t> E , finally, HBV virion secreted in supernatant was captured 72 h after ligand treatment, and its DNA was quantitated by qPCR. The virion secretion in the presence of calcitriol was marginally reduced in all HBV cell culture models (up to 12%) in vitro , though the observation was not statistically significant in any model. All data are means ± SD for three independent experiments (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, and NS (analyzed by paired Student's t test). HBeAg, hepatitis B “e” antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; NS, not significant; NTCP, sodium taurocholate cotransporting polypeptide; pcRNA, precore RNA; pgRNA, pregenomic RNA.
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enzyme-linked immunosorbent assay test ortho hcv 3.0  (Diagnostica Stago)
90
Diagnostica Stago enzyme-linked immunosorbent assay test ortho hcv 3.0
Calcitriol inhibits HBV core promoter transcripts, HBV secretory proteins, but not HBV virion secretion. The 1.3×-HBV genome construct was transfected in HepG2 and Huh7 cells, whereas HepG2.2.15 stably expresses HBV genome. In the HBV infection model, HBV particles derived from HepG2.2.15 cells were used to infect HepG2-NTCP cells as described in the section. Vehicle control (without calcitriol) or 10 nM calcitriol was added immediately after transfection or infection, and samples were processed as described in the section. RNA isolation and quantitation by quantitative PCR (qPCR) shows that ( A ) HBV pcRNA and ( B ) HBV pgRNA are suppressed in the presence of calcitriol. Quantitation of HBV secretory proteins by <t>ELISA</t> demonstrates that calcitriol negatively regulates ( C ) HBeAg and ( D ) <t>HBsAg.</t> E , finally, HBV virion secreted in supernatant was captured 72 h after ligand treatment, and its DNA was quantitated by qPCR. The virion secretion in the presence of calcitriol was marginally reduced in all HBV cell culture models (up to 12%) in vitro , though the observation was not statistically significant in any model. All data are means ± SD for three independent experiments (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, and NS (analyzed by paired Student's t test). HBeAg, hepatitis B “e” antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; NS, not significant; NTCP, sodium taurocholate cotransporting polypeptide; pcRNA, precore RNA; pgRNA, pregenomic RNA.
Enzyme Linked Immunosorbent Assay Test Ortho Hcv 3.0, supplied by Diagnostica Stago, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Characteristics of studies included in the systematic review on HCV antibody detection from DBS compared to venous blood sampling

Journal: BMC Infectious Diseases

Article Title: Diagnostic accuracy of serological diagnosis of hepatitis C and B using dried blood spot samples (DBS): two systematic reviews and meta-analyses

doi: 10.1186/s12879-017-2777-y

Figure Lengend Snippet: Characteristics of studies included in the systematic review on HCV antibody detection from DBS compared to venous blood sampling

Article Snippet: Kania Burkina-Faso 2013 , Cross sectional , 218 HIV screening participants, 5 anti-HCV pos, 213 anti-HCV neg , NR , Venipuncture, 5 spots whole blood (50 μl) on Whatman 903 , Monolisa HCV-Ab-Ag ULTRA assay (Bio-Rad), further assessment with Inno-Lia HCV Score assay (Innogenetics) , Monolisa HCV-Ab-Ag ULTRA assay (Bio-Rad), further assessment with Inno-Lia HCV Score assay (Innogenetics) , 0.439 , 100% (97,8–100%) , 100% (46,3–100%) , kappa: 1,00 (0,93–1,00) , NR.

Techniques: Derivative Assay, Enzyme-linked Immunosorbent Assay, Luminex, Diagnostic Assay, Western Blot, Infection

Forest plot of sensitivity and specificity of hepatitis C antibody detection in DBS samples compared to venous blood samples

Journal: BMC Infectious Diseases

Article Title: Diagnostic accuracy of serological diagnosis of hepatitis C and B using dried blood spot samples (DBS): two systematic reviews and meta-analyses

doi: 10.1186/s12879-017-2777-y

Figure Lengend Snippet: Forest plot of sensitivity and specificity of hepatitis C antibody detection in DBS samples compared to venous blood samples

Article Snippet: Kania Burkina-Faso 2013 , Cross sectional , 218 HIV screening participants, 5 anti-HCV pos, 213 anti-HCV neg , NR , Venipuncture, 5 spots whole blood (50 μl) on Whatman 903 , Monolisa HCV-Ab-Ag ULTRA assay (Bio-Rad), further assessment with Inno-Lia HCV Score assay (Innogenetics) , Monolisa HCV-Ab-Ag ULTRA assay (Bio-Rad), further assessment with Inno-Lia HCV Score assay (Innogenetics) , 0.439 , 100% (97,8–100%) , 100% (46,3–100%) , kappa: 1,00 (0,93–1,00) , NR.

Techniques:

Calcitriol inhibits HBV core promoter transcripts, HBV secretory proteins, but not HBV virion secretion. The 1.3×-HBV genome construct was transfected in HepG2 and Huh7 cells, whereas HepG2.2.15 stably expresses HBV genome. In the HBV infection model, HBV particles derived from HepG2.2.15 cells were used to infect HepG2-NTCP cells as described in the section. Vehicle control (without calcitriol) or 10 nM calcitriol was added immediately after transfection or infection, and samples were processed as described in the section. RNA isolation and quantitation by quantitative PCR (qPCR) shows that ( A ) HBV pcRNA and ( B ) HBV pgRNA are suppressed in the presence of calcitriol. Quantitation of HBV secretory proteins by ELISA demonstrates that calcitriol negatively regulates ( C ) HBeAg and ( D ) HBsAg. E , finally, HBV virion secreted in supernatant was captured 72 h after ligand treatment, and its DNA was quantitated by qPCR. The virion secretion in the presence of calcitriol was marginally reduced in all HBV cell culture models (up to 12%) in vitro , though the observation was not statistically significant in any model. All data are means ± SD for three independent experiments (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, and NS (analyzed by paired Student's t test). HBeAg, hepatitis B “e” antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; NS, not significant; NTCP, sodium taurocholate cotransporting polypeptide; pcRNA, precore RNA; pgRNA, pregenomic RNA.

Journal: The Journal of Biological Chemistry

Article Title: Vitamin D signaling inhibits HBV activity by directly targeting the HBV core promoter

doi: 10.1016/j.jbc.2021.101233

Figure Lengend Snippet: Calcitriol inhibits HBV core promoter transcripts, HBV secretory proteins, but not HBV virion secretion. The 1.3×-HBV genome construct was transfected in HepG2 and Huh7 cells, whereas HepG2.2.15 stably expresses HBV genome. In the HBV infection model, HBV particles derived from HepG2.2.15 cells were used to infect HepG2-NTCP cells as described in the section. Vehicle control (without calcitriol) or 10 nM calcitriol was added immediately after transfection or infection, and samples were processed as described in the section. RNA isolation and quantitation by quantitative PCR (qPCR) shows that ( A ) HBV pcRNA and ( B ) HBV pgRNA are suppressed in the presence of calcitriol. Quantitation of HBV secretory proteins by ELISA demonstrates that calcitriol negatively regulates ( C ) HBeAg and ( D ) HBsAg. E , finally, HBV virion secreted in supernatant was captured 72 h after ligand treatment, and its DNA was quantitated by qPCR. The virion secretion in the presence of calcitriol was marginally reduced in all HBV cell culture models (up to 12%) in vitro , though the observation was not statistically significant in any model. All data are means ± SD for three independent experiments (n = 3). ∗ p < 0.05, ∗∗ p < 0.01, and NS (analyzed by paired Student's t test). HBeAg, hepatitis B “e” antigen; HBsAg, hepatitis B surface antigen; HBV, hepatitis B virus; NS, not significant; NTCP, sodium taurocholate cotransporting polypeptide; pcRNA, precore RNA; pgRNA, pregenomic RNA.

Article Snippet: Secreted HBsAg was quantitated using HBsAg ELISA plates (MONOLISA; Bio-Rad), whereas HBeAg was quantitated on HBeAg ELISA plates (Diasorin) as per the manufacturer's instructions ( ).

Techniques: Construct, Transfection, Stable Transfection, Infection, Derivative Assay, Isolation, Quantitation Assay, Real-time Polymerase Chain Reaction, Enzyme-linked Immunosorbent Assay, Cell Culture, In Vitro