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density od value  (Tecan Systems)


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    Tecan Systems density od value
    Density Od Value, supplied by Tecan Systems, used in various techniques. Bioz Stars score: 99/100, based on 16944 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/density+od+values/Spark/pm40451556-104-2-16
    Average 99 stars, based on 16944 article reviews
    density od value - by Bioz Stars, 2026-09
    99/100 stars

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    other:

    Article Title: Targeted Degradation of SOS1 Exhibits Potent Anticancer Activity and Overcomes Resistance in KRAS-Mutant Tumors and BCR-ABL-Positive Leukemia
    Article Snippet: The optical density (OD) values were obtained using a SPARK microplate reader (TECAN, Switzerland).

    Article Title: Exploring the Antimicrobial Potential of Hallachrome, a Defensive Anthraquinone from the Marine Worm Halla parthenopeia (Polychaeta)
    Article Snippet: Results were expressed as optical density (OD) values at 595 nm using a microplate reader (Sunrise Tecan, Grödig, Austria).

    Article Title: Targeted Degradation of SOS1 Exhibits Potent Anticancer Activity and Overcomes Resistance in KRAS-Mutant Tumors and BCR–ABL–Positive Leukemia
    Article Snippet: The optical density (OD) values were obtained using a SPARK microplate reader (Tecan).

    Article Title: AAV ‐mediated gene therapy restores natural fertility and improves physical function in the Lhcgr ‐deficient mouse model of Leydig cell failure
    Article Snippet: The optical density (OD) values were recorded at 450 ± 10 nm and measured by a microplate reader (Sunrise, TECAN).

    Article Title: AAV-mediated gene therapy restores natural fertility and improves physical function in the Lhcgr-deficient mouse model of Leydig cell failure.
    Article Snippet: The optical density (OD) values were recorded at 450 ± 10 nm and measured by a microplate reader (Sunrise, TECAN).

    Article Title: Exploring the Antimicrobial Potential of Hallachrome, a Defensive Anthraquinone from the Marine Worm Halla parthenopeia (Polychaeta)
    Article Snippet: Results were expressed as optical density (OD) values at 595 nm using a microplate reader (Sunrise Tecan, Grödig, Austria).

    Article Title: Celastrol Ameliorates Hypoxia-Induced Pulmonary Hypertension by Regulation of the PDE5-cGMP-PKG Signaling Pathway.
    Article Snippet: Pulmonary hypertension (PH) is a severe pulmonary vascular disease characterized by poor clinical outcomes and limited therapeutic options.. Celastrol (CEL), a natural product derived from Tripterygium wilfordii Hook F, has shown therapeutic potential in PH models, although its mechanisms are not fully understood.. This study aims to investigate the role of CEL in PH and explore its potential underlying mechanisms.

    Incubation:

    Article Title: Flowable resin-based composites modified with chlorhexidine-loaded mesoporous silica nanoparticles induce superior antibiofilm properties
    Article Snippet: .. After incubation for 24 h, the supernatant was discarded and 150 μl of APH buffer was added in each well and plates were incubated under 5% CO2 at 37 °C for 1.5 h, followed by addition of 20 μl of 1 M of NaOH and incubated for 10 min. Then the optical density (OD) values were measured using microplate reader (SunriseTM, Tecan, Switzerland) at the wavelength of 405 nm. ..



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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 <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