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Valiant Co Ltd trypan blue tb
Trypan Blue Tb, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 96/100, based on 176 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Characterization:

Article Title: Evaluating the regenerative capacity of biosynthesized nano formulated 3D scaffolds in scald burn healing
Article Snippet: .. The cell pellet was suspended in 1 mL PBS and manual cell count was performed using a Neubauer chamber with the aid of 0.4% trypan blue (MP Biomedicals Inc; 195332) used in a ratio of 1 : 1. ..

other:

Article Title: Safety and efficacy of a STAT3-targeted cyclic oligonucleotide: From murine models to a phase 1 clinical trial in pet cats with oral cancer
Article Snippet: Article Safety and efficacy of a STAT3-targeted cyclic oligonucleotide: From murine models to a phase 1 clinical trial in pet cats with oral cancer Graphical abstract Highlights • Cyclic STAT3 decoy (CS3D) inhibits murine HNSCC tumors via CD8+ cells • CS3D is well tolerated in a clinical trial of pet cats with oral cancer • CS3D induces a 35% disease control rate in pet cats with oral cancer • Analysis of the clinical trial specimens identifies potential predictive biomarkers Authors Jennifer R. Grandis, Katherine A. Skorupski, Ning Cheng, ..., Adam B. Olshen, Ellen E. Sparger, Daniel E. Johnson Correspondence jennifer.grandis@ucsf.edu (J.R.G.), daniel.johnson@ucsf.edu (D.E.J.). In brief Grandis et al. evaluate the activity of a cyclic oligonucleotide inhibitor of STAT3, CS3D, in immunocompetent models of mouse head and neck cancer and in a clinical trial of pet cats with oral cancer.. CS3D has low toxicity and modulation of immune parameters is associated with anti-tumor activity.

Article Title: Trilaciclib triggers a neutrophil-related immune response and sensitizes non-small cell lung cancer to anti-PD-1 therapy
Article Snippet: The protein expression levels of CXCL2 in tumor cells CM and IL-12b in TANs CM were measured by using human enzyme-linked immunosorbent assay (ELISA) kit (Elabscience, Cat. #E-EL-H1904, Cat. #E-EL-H0151) according to the manufacturer’s instructions.

Incubation:

Article Title: Modeling effective doses of therapeutic antibodies targeting clustered surface receptors
Article Snippet: .. After 72 hours incubation at 37°C in 5% CO2 incubator, the number of living cells was counted using trypan blue (MP Biomedicals, Santa Ana, CA) from one row of cells via hemocytometer with counts graphed on Prism 9 software (GraphPad, San Diego, CA). .. ACCEPTED MANUSCRIPT AR TIC LE IN PR ES S ARTICLE IN PRESS After 7 days incubation at 37°C in 5% CO2 incubator with no media changes, 200 l of the cell supernatants were collected from the remaining two rows of cells into labelled 1.5 ml microcentrifuge tubes (Thermo Fisher Scientific) by antibody dilution and stored at -80°C until use.

Incubator:

Article Title: Modeling effective doses of therapeutic antibodies targeting clustered surface receptors
Article Snippet: .. After 72 hours incubation at 37°C in 5% CO2 incubator, the number of living cells was counted using trypan blue (MP Biomedicals, Santa Ana, CA) from one row of cells via hemocytometer with counts graphed on Prism 9 software (GraphPad, San Diego, CA). .. ACCEPTED MANUSCRIPT AR TIC LE IN PR ES S ARTICLE IN PRESS After 7 days incubation at 37°C in 5% CO2 incubator with no media changes, 200 l of the cell supernatants were collected from the remaining two rows of cells into labelled 1.5 ml microcentrifuge tubes (Thermo Fisher Scientific) by antibody dilution and stored at -80°C until use.

Software:

Article Title: Modeling effective doses of therapeutic antibodies targeting clustered surface receptors
Article Snippet: .. After 72 hours incubation at 37°C in 5% CO2 incubator, the number of living cells was counted using trypan blue (MP Biomedicals, Santa Ana, CA) from one row of cells via hemocytometer with counts graphed on Prism 9 software (GraphPad, San Diego, CA). .. ACCEPTED MANUSCRIPT AR TIC LE IN PR ES S ARTICLE IN PRESS After 7 days incubation at 37°C in 5% CO2 incubator with no media changes, 200 l of the cell supernatants were collected from the remaining two rows of cells into labelled 1.5 ml microcentrifuge tubes (Thermo Fisher Scientific) by antibody dilution and stored at -80°C until use.

Staining:

Article Title: Methods and compositions for targeting cancer cells in metastases
Article Snippet: .. Following treatment with either HK-BLMP6 (0.1 mM) or HK-BLMP5 (0.3 mM) in 0.5 ml serum free culture media for 8 hours, cells were stained with 0.4% Trypan Blue solution (MP Biomedicals) (Daquinag et al., 2016). .. For radioactive studies, 1,4,7,10-tetraazacyclotetradecane-N′,N′′,N′′′,N′′′′-tetra-acetic acid (DOTA) t-Bu ester was purchased from Macrocyclics (Dallas, TX) and peptides were synthesized by Bachem Americas (Torrance, CA).

Article Title: Trilaciclib triggers a neutrophil-related immune response and sensitizes non-small cell lung cancer to anti-PD-1 therapy.
Article Snippet: .. The purity and cell viability of neutrophils were assessed by Trypan blue (MP Biomedicals, LLC) exclusion and Wright/Giemsa staining, respectively. ..



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IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple, n = 8) or Hoti (green, n = 6). The clinical score (A) , summarizing appearance, behavior, body weight ( B ), and body temperature ( C ), was monitored daily. After reaching the clinical endpoint (score of ≥10 or ≥6 on two consecutive days), the mice were euthanized or found dead (terminal, gray). Asterisk indicates mice that have died. Dotted lines mark the clinical endpoints.

Journal: npj Viruses

Article Title: Side-by-side evaluation of two Crimean-Congo hemorrhagic fever virus isolates in IFNAR −/− mice

doi: 10.1038/s44298-026-00216-2

Figure Lengend Snippet: IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple, n = 8) or Hoti (green, n = 6). The clinical score (A) , summarizing appearance, behavior, body weight ( B ), and body temperature ( C ), was monitored daily. After reaching the clinical endpoint (score of ≥10 or ≥6 on two consecutive days), the mice were euthanized or found dead (terminal, gray). Asterisk indicates mice that have died. Dotted lines mark the clinical endpoints.

Article Snippet: Microtiter plates were coated with CCHFV glycoprotein (Gc) protein ( REC31696 , The Native Antigen Company, Oxford, United Kingdom) diluted to 0.5 μg/ml in phosphate-buffered saline (PBS) and incubated for 20 h at 4 °C.

Techniques: Infection

IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple, n = 8) or Hoti (green, n = 6). A CCHFV genome copy was measured by RT-qPCR in organs and serum samples (day 3 and final) of individual mice. B Infectious CCHFV was determined by TCID 50 assay in organs and final serum samples of individual mice. Each data point represents a sample from an individual animal, data are shown as the means ± SD. Datasets were analyzed using Šídák’s multiple comparisons test ( A ) or Tukey’s multiple comparisons test ( B ). Asterisks indicate statistical significance as detailed between CCHFV Afg09 and Kosovo Hoti group: ∗ p ≤ 0.05; ∗∗∗∗ p < 0.0001.

Journal: npj Viruses

Article Title: Side-by-side evaluation of two Crimean-Congo hemorrhagic fever virus isolates in IFNAR −/− mice

doi: 10.1038/s44298-026-00216-2

Figure Lengend Snippet: IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple, n = 8) or Hoti (green, n = 6). A CCHFV genome copy was measured by RT-qPCR in organs and serum samples (day 3 and final) of individual mice. B Infectious CCHFV was determined by TCID 50 assay in organs and final serum samples of individual mice. Each data point represents a sample from an individual animal, data are shown as the means ± SD. Datasets were analyzed using Šídák’s multiple comparisons test ( A ) or Tukey’s multiple comparisons test ( B ). Asterisks indicate statistical significance as detailed between CCHFV Afg09 and Kosovo Hoti group: ∗ p ≤ 0.05; ∗∗∗∗ p < 0.0001.

Article Snippet: Microtiter plates were coated with CCHFV glycoprotein (Gc) protein ( REC31696 , The Native Antigen Company, Oxford, United Kingdom) diluted to 0.5 μg/ml in phosphate-buffered saline (PBS) and incubated for 20 h at 4 °C.

Techniques: Infection, Quantitative RT-PCR

IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple) or Hoti (green). A Final sera (Afg09 n = 6, Hoti n = 6) were analyzed with two virus-specific ELISAs using either inactivated CCHFV, measuring NP-specific antibodies, or the major glycoprotein Gc for coating. Monoclonal antibodies detecting Gc or N protein were used as controls (not shown). Dotted lines indicate the respective cut-off. B Liver enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed in final serum samples (Afg09 n = 5, Hoti n = 3). Dotted lines indicate the physiological range of healthy C57BL/6 mice .

Journal: npj Viruses

Article Title: Side-by-side evaluation of two Crimean-Congo hemorrhagic fever virus isolates in IFNAR −/− mice

doi: 10.1038/s44298-026-00216-2

Figure Lengend Snippet: IFNAR −/− mice were infected with either 100 TCID 50 CCHFV Afg09 (purple) or Hoti (green). A Final sera (Afg09 n = 6, Hoti n = 6) were analyzed with two virus-specific ELISAs using either inactivated CCHFV, measuring NP-specific antibodies, or the major glycoprotein Gc for coating. Monoclonal antibodies detecting Gc or N protein were used as controls (not shown). Dotted lines indicate the respective cut-off. B Liver enzymes alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were analyzed in final serum samples (Afg09 n = 5, Hoti n = 3). Dotted lines indicate the physiological range of healthy C57BL/6 mice .

Article Snippet: Microtiter plates were coated with CCHFV glycoprotein (Gc) protein ( REC31696 , The Native Antigen Company, Oxford, United Kingdom) diluted to 0.5 μg/ml in phosphate-buffered saline (PBS) and incubated for 20 h at 4 °C.

Techniques: Infection, Virus, Bioprocessing

Liver, spleen and brain of CCHFV Afg09 (purple) or Hoti-infected (green) IFNAR −/− mice were pathologically examined post-mortem. A Shown are exemplary images of organ histopathology, H&E (hematoxylin and eosin) staining; ISH (in situ hybridization). Arrows indicate multifocal liver necrosis with loss of tissue architecture and lymphohistiocytic infiltrates. Arrowheads indicate apoptosis in germinal follicle centers. Scale bars: 100 µm. B Quantification of ISH indicating percentage area of CCHFV-positive organ sections. Each data point represents a sample from an individual animal, and horizontal lines represent the means ± SD. Datasets were analyzed using Šídák’s multiple comparisons test. Asterisks indicate statistical significance as detailed between CCHFV Afg09 and Kosovo Hoti group: ∗∗∗∗ p < 0.0001; ns = not significant.

Journal: npj Viruses

Article Title: Side-by-side evaluation of two Crimean-Congo hemorrhagic fever virus isolates in IFNAR −/− mice

doi: 10.1038/s44298-026-00216-2

Figure Lengend Snippet: Liver, spleen and brain of CCHFV Afg09 (purple) or Hoti-infected (green) IFNAR −/− mice were pathologically examined post-mortem. A Shown are exemplary images of organ histopathology, H&E (hematoxylin and eosin) staining; ISH (in situ hybridization). Arrows indicate multifocal liver necrosis with loss of tissue architecture and lymphohistiocytic infiltrates. Arrowheads indicate apoptosis in germinal follicle centers. Scale bars: 100 µm. B Quantification of ISH indicating percentage area of CCHFV-positive organ sections. Each data point represents a sample from an individual animal, and horizontal lines represent the means ± SD. Datasets were analyzed using Šídák’s multiple comparisons test. Asterisks indicate statistical significance as detailed between CCHFV Afg09 and Kosovo Hoti group: ∗∗∗∗ p < 0.0001; ns = not significant.

Article Snippet: Microtiter plates were coated with CCHFV glycoprotein (Gc) protein ( REC31696 , The Native Antigen Company, Oxford, United Kingdom) diluted to 0.5 μg/ml in phosphate-buffered saline (PBS) and incubated for 20 h at 4 °C.

Techniques: Infection, Histopathology, Staining, In Situ Hybridization