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optical density od values  (BMG Labtech)


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    BMG Labtech optical density od values
    Optical Density Od Values, supplied by BMG Labtech, used in various techniques. Bioz Stars score: 99/100, based on 8745 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/optical+density+od+values/CLARIOstar+Plus/pmc12255919-93-0-12
    Average 99 stars, based on 8745 article reviews
    optical density od values - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    other:

    Article Title: Investigation of endoplasmic reticulum stress parameters in patients with gestational diabetes mellitus: A prospective study
    Article Snippet: Optical density (OD) values were measured with a CLARIOstar microtiter plate reader (BMG LABTECH, Offenburg, Germany) at a wavelength of 450 nm.

    Incubation:

    Article Title: Repurposed drug agomelatine is therapeutic against collagen-induced arthritis via iNOS targeting.
    Article Snippet: Background: The most promising biologics tumor necrosis factor α (TNFα) inhibitors are effective in treating rheumatoid arthritis (RA) in only 50–70 % of the cases; thus, new drugs targeting TNFα-mediated inflammation

    Concentration Assay:

    Article Title: Therapeutic targeting of siRNA/anti-cancer drug delivery system for non-melanoma skin cancer. Part I: Development and gene silencing of JAK1siRNA/5-FU loaded liposome nanocomplexes.
    Article Snippet: Non-melanoma skin cancer (NMSC) is one of the most prevalent cancers, leading to significant mortality rates due to limited treatment options and a lack of effective therapeutics.. Janus kinase (JAK1), a non-receptor tyrosine kinase family member, is involved in various cellular processes, including differentiation, cell proliferation and survival, playing a crucial role in cancer progression.. This study aims to provide a more effective treatment for NMSC by concurrently silencing the JAK1 gene and administering 5-Fluorouracil (5-FU) using liposome nanocomplexes as delivery vehicles.



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    Figure 3. This figure illustrates the <t>optical</t> <t>density</t> (OD) <t>values</t> representing IgG antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgG Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgG Ab levels and beta CCCoV-specific IgG Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgG Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.
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    Figure 3. This figure illustrates the <t>optical</t> <t>density</t> (OD) <t>values</t> representing IgG antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgG Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgG Ab levels and beta CCCoV-specific IgG Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgG Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.
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    Figure 3. This figure illustrates the <t>optical</t> <t>density</t> (OD) <t>values</t> representing IgG antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgG Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgG Ab levels and beta CCCoV-specific IgG Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgG Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.
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    Figure 3. This figure illustrates the optical density (OD) values representing IgG antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgG Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgG Ab levels and beta CCCoV-specific IgG Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgG Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Journal: Vaccines

    Article Title: Circulating Antibodies Against Common Cold Coronaviruses Do Not Interfere with Immune Responses to Primary or Booster SARS-CoV-2 mRNA Vaccines.

    doi: 10.3390/vaccines13050547

    Figure Lengend Snippet: Figure 3. This figure illustrates the optical density (OD) values representing IgG antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgG Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgG Ab levels and beta CCCoV-specific IgG Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgG Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Article Snippet: The development of the plates followed previously described methods, and optical density (OD) values were measured at 650 nm using SoftMax Pro 7.1 software (Molecular Devices, LLC, San Jose, CA, USA).

    Techniques: Virus

    Figure 4. This figure illustrates the optical density (OD) values representing IgA antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgA Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgA Ab levels and beta CCCoV-specific IgA Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgA Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Journal: Vaccines

    Article Title: Circulating Antibodies Against Common Cold Coronaviruses Do Not Interfere with Immune Responses to Primary or Booster SARS-CoV-2 mRNA Vaccines.

    doi: 10.3390/vaccines13050547

    Figure Lengend Snippet: Figure 4. This figure illustrates the optical density (OD) values representing IgA antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of the IgG antibody against CCCoVs. The left column displays IgA Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgA Ab levels and beta CCCoV-specific IgA Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgA Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Article Snippet: The development of the plates followed previously described methods, and optical density (OD) values were measured at 650 nm using SoftMax Pro 7.1 software (Molecular Devices, LLC, San Jose, CA, USA).

    Techniques: Virus

    Figure 5. This figure illustrates the optical density (OD) values representing IgM antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of IgG antibody against CCCoVs. The left column displays IgM Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgM Ab levels and beta CCCoV-specific IgM Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgM Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Journal: Vaccines

    Article Title: Circulating Antibodies Against Common Cold Coronaviruses Do Not Interfere with Immune Responses to Primary or Booster SARS-CoV-2 mRNA Vaccines.

    doi: 10.3390/vaccines13050547

    Figure Lengend Snippet: Figure 5. This figure illustrates the optical density (OD) values representing IgM antibody (Ab) levels against conserved and specific antigens of seasonal common cold coronaviruses (CCCoVs) across seven time points: pre-vaccination (Pre), first vaccine dose (Vax1), second vaccine dose (Vax2), 6 months post-vaccination (6 m), 9 months post-vaccination (9 m), 12 months post-vaccination (12 m), and 15 months post-vaccination (15 m). Serum samples were diluted 1:100 for the detection of IgG antibody against CCCoVs. The left column displays IgM Ab levels against alpha CCCoVs (A,C,E,G), while the right column represents beta CCCoVs (B,D,F,H). Alpha CCCoV-specific IgM Ab levels and beta CCCoV-specific IgM Ab levels were measured using S protein (RBD) and N protein peptide ELISAs. The graphs are subdivided into anti-S Ab levels (top two rows) and anti-N Ab levels (bottom two rows) for each virus. Additionally, the bottom-most row shows IgM Ab levels against conserved N peptides for alpha CCCoVs (I) and beta CCCoVs (J). The red dots indicate individual data points, with lines connecting mean OD values across time points; different letters indicate statistically significant differences. Different time points that share the same letter are not significantly different from each other, while the time points with different letters indicate significant differences (p < 0.05). Data are presented as mean ± SEM.

    Article Snippet: The development of the plates followed previously described methods, and optical density (OD) values were measured at 650 nm using SoftMax Pro 7.1 software (Molecular Devices, LLC, San Jose, CA, USA).

    Techniques: Virus