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LabCorp hcv rna
Hcv Rna, supplied by LabCorp, 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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Reverse Transcription Polymerase Chain Reaction:

Article Title: Algorithmic Approach to High-Throughput Molecular Screening for Alpha Interferon-Resistant Genotypes in Hepatitis C Patients
Article Snippet: .. Seventy-two serum samples which were defined by reverse transcription-PCR (RT-PCR) as having detectable levels of HCV RNA were obtained from LabCorp (Center for Molecular Biology and Pathology, Research Triangle Park, N.C.). .. RNA was extracted from approximately 100 μl of serum with a commercially available extraction kit (Puregene; RNA extraction systems; Gentra Systems, Minneapolis, Minn.) and was resuspended in 30 μl of RNase-free distilled water.

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Article Title: Structural Bone Deficits in HIV/HCV-Coinfected, HCV-Monoinfected, and HIV-Monoinfected Women
Article Snippet: For chronically HCV-infected participants, we collected the most recent HBsAg, HCV RNA, creatinine, and METAVIR stage of hepatic fibrosis by liver biopsy [ ], HCV FibroSure test (Laboratory Corporation of America, Burlington, North Carolina) [ ], or Hepascore test (Quest Diagnostics, San Juan Capistrano, California) [ ].

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    LabCorp hcv rna hcv rna
    ( a–d ) Force–distance curves for target <t>HCV</t> <t>RNA</t> (6.0 fM) were recorded within a 150 nm × 150 nm area with a lateral pixel size of 10 nm. The number in each pixel represents the percentage of getting the specific event. The diameter of the clusters was within 30–60 nm. The pixels with the red circle showed the mean value out of the range (22–42 pN). ( e ) Adhesion force map of a 900 nm × 900 nm area with a lateral pixel size of 20 nm, obtained using target HCV RNA (5.7 fM). Mean force values were categorized into four levels, indicated by different colors. Isolated pixels are marked with red circles and clusters with blue circles.
    Hcv Rna Hcv Rna, supplied by LabCorp, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hcv rna hcv rna/product/LabCorp
    Average 85 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    hcv rna hcv rna - by Bioz Stars, 2020-05
    85/100 stars
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    ( a–d ) Force–distance curves for target HCV RNA (6.0 fM) were recorded within a 150 nm × 150 nm area with a lateral pixel size of 10 nm. The number in each pixel represents the percentage of getting the specific event. The diameter of the clusters was within 30–60 nm. The pixels with the red circle showed the mean value out of the range (22–42 pN). ( e ) Adhesion force map of a 900 nm × 900 nm area with a lateral pixel size of 20 nm, obtained using target HCV RNA (5.7 fM). Mean force values were categorized into four levels, indicated by different colors. Isolated pixels are marked with red circles and clusters with blue circles.

    Journal: Nucleic Acids Research

    Article Title: Direct quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification

    doi: 10.1093/nar/gks953

    Figure Lengend Snippet: ( a–d ) Force–distance curves for target HCV RNA (6.0 fM) were recorded within a 150 nm × 150 nm area with a lateral pixel size of 10 nm. The number in each pixel represents the percentage of getting the specific event. The diameter of the clusters was within 30–60 nm. The pixels with the red circle showed the mean value out of the range (22–42 pN). ( e ) Adhesion force map of a 900 nm × 900 nm area with a lateral pixel size of 20 nm, obtained using target HCV RNA (5.7 fM). Mean force values were categorized into four levels, indicated by different colors. Isolated pixels are marked with red circles and clusters with blue circles.

    Article Snippet: Preparation of HCV RNA HCV RNA, which was single-stranded and 9.6 kb in length, was provided by the Laboratory Corporation of America (LabCorp).

    Techniques: Isolation

    Secondary structures of 5′ non-coding region (nucleotides 3–263) of HCV RNA ( http://rna.tbi.univie.ac.at/cgi-bin/RNAfold.cgi ). There are two major RNA secondary structures of which minimum free energy is ( a ) −98.95 kcal/mol and ( b ) −97.30 kcal/mol, respectively. Three sub-domains that were completely invariant among seven major genotypes of HCV RNA were indicated by blue (positions from 3 to 65), orange (positions from 178 to 199) and pink (positions 246 to 263).

    Journal: Nucleic Acids Research

    Article Title: Direct quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification

    doi: 10.1093/nar/gks953

    Figure Lengend Snippet: Secondary structures of 5′ non-coding region (nucleotides 3–263) of HCV RNA ( http://rna.tbi.univie.ac.at/cgi-bin/RNAfold.cgi ). There are two major RNA secondary structures of which minimum free energy is ( a ) −98.95 kcal/mol and ( b ) −97.30 kcal/mol, respectively. Three sub-domains that were completely invariant among seven major genotypes of HCV RNA were indicated by blue (positions from 3 to 65), orange (positions from 178 to 199) and pink (positions 246 to 263).

    Article Snippet: Preparation of HCV RNA HCV RNA, which was single-stranded and 9.6 kb in length, was provided by the Laboratory Corporation of America (LabCorp).

    Techniques:

    ( a ) Schematic of the experimental setup employed for the force mapping described in this study. Force measurements were recorded at a pulling rate of 0.70 μm/s between the detection DNA and the captured HCV RNA on the surface. The 18-mer detection DNA probe (green) complementary to nucleotides 246–263 of the HCV RNA (pink) was immobilized on the 27-acid dendron-modified AFM tip. The 60-mer capture probe DNA complementary to nucleotides 3–62 of the HCV RNA (blue) was immobilized on a 27-acid dendron-modified silicon substrate. Typical force–distance curve with ( b ) a single rupture and ( c ) multiple ruptures between the detection probe DNA and the complementary part of the HCV RNA.

    Journal: Nucleic Acids Research

    Article Title: Direct quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification

    doi: 10.1093/nar/gks953

    Figure Lengend Snippet: ( a ) Schematic of the experimental setup employed for the force mapping described in this study. Force measurements were recorded at a pulling rate of 0.70 μm/s between the detection DNA and the captured HCV RNA on the surface. The 18-mer detection DNA probe (green) complementary to nucleotides 246–263 of the HCV RNA (pink) was immobilized on the 27-acid dendron-modified AFM tip. The 60-mer capture probe DNA complementary to nucleotides 3–62 of the HCV RNA (blue) was immobilized on a 27-acid dendron-modified silicon substrate. Typical force–distance curve with ( b ) a single rupture and ( c ) multiple ruptures between the detection probe DNA and the complementary part of the HCV RNA.

    Article Snippet: Preparation of HCV RNA HCV RNA, which was single-stranded and 9.6 kb in length, was provided by the Laboratory Corporation of America (LabCorp).

    Techniques: Modification

    The histograms of the unbinding force ( a ) and the distance ( b ) derived from the force–distance curves of the interaction recorded on an area (150 nm × 150 nm) for a sample of 6.0 fM HCV RNA. The mean value of unbinding force was 32 ± 5 (the force value ± σ) pN (a) and the unbinding distance ranged from 8 nm to 70 nm (b). The probability of getting the specific event was 34%.

    Journal: Nucleic Acids Research

    Article Title: Direct quantitative analysis of HCV RNA by atomic force microscopy without labeling or amplification

    doi: 10.1093/nar/gks953

    Figure Lengend Snippet: The histograms of the unbinding force ( a ) and the distance ( b ) derived from the force–distance curves of the interaction recorded on an area (150 nm × 150 nm) for a sample of 6.0 fM HCV RNA. The mean value of unbinding force was 32 ± 5 (the force value ± σ) pN (a) and the unbinding distance ranged from 8 nm to 70 nm (b). The probability of getting the specific event was 34%.

    Article Snippet: Preparation of HCV RNA HCV RNA, which was single-stranded and 9.6 kb in length, was provided by the Laboratory Corporation of America (LabCorp).

    Techniques: Derivative Assay

    Box plot Distribution of HCV RNA in lipid fractions. HCV RNA levels were higher in lowest density (1) compared to highest density (15) fractions, with no significant changes in co-localization of HCV RNA with statin therapy. The box plots summarize the distribution of HCV RNA for all 11 patients at four study intervals. The box extends to the 25th and 75th quantiles, with the median HCV RNA shown as horizontal line within the box. The whiskers (shown as vertical dash lines) extend from the ends of the box to the outermost data point.

    Journal: Journal of viral hepatitis

    Article Title: Open-label, ascending dose, prospective cohort study evaluating the antiviral efficacy of Rosuvastatin therapy in serum and lipid fractions in patients with chronic hepatitis C

    doi: 10.1111/j.1365-2893.2010.01310.x

    Figure Lengend Snippet: Box plot Distribution of HCV RNA in lipid fractions. HCV RNA levels were higher in lowest density (1) compared to highest density (15) fractions, with no significant changes in co-localization of HCV RNA with statin therapy. The box plots summarize the distribution of HCV RNA for all 11 patients at four study intervals. The box extends to the 25th and 75th quantiles, with the median HCV RNA shown as horizontal line within the box. The whiskers (shown as vertical dash lines) extend from the ends of the box to the outermost data point.

    Article Snippet: Blood samples were stored at −70 °C for HCV RNA quantification in serum and in lipid fractions by the HCV Superquant assay (NGI Labcorp, Los Angeles, CA, USA).

    Techniques:

    HCV RNA change in individual patients based on Rosuvastatin dosing schedule. There were no significant declines in HCV RNA during therapy, except for one patient (bold line) with a 1.85 log decline at 40 mg dosing that may represent a sampling issue, as there was no concurrent decline at this time point in the lipid fraction analysis.

    Journal: Journal of viral hepatitis

    Article Title: Open-label, ascending dose, prospective cohort study evaluating the antiviral efficacy of Rosuvastatin therapy in serum and lipid fractions in patients with chronic hepatitis C

    doi: 10.1111/j.1365-2893.2010.01310.x

    Figure Lengend Snippet: HCV RNA change in individual patients based on Rosuvastatin dosing schedule. There were no significant declines in HCV RNA during therapy, except for one patient (bold line) with a 1.85 log decline at 40 mg dosing that may represent a sampling issue, as there was no concurrent decline at this time point in the lipid fraction analysis.

    Article Snippet: Blood samples were stored at −70 °C for HCV RNA quantification in serum and in lipid fractions by the HCV Superquant assay (NGI Labcorp, Los Angeles, CA, USA).

    Techniques: Sampling