Journal: Molecular Cytogenetics

Article Title: Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

doi: 10.1186/s13039-020-00511-4

Figure Lengend Snippet: a Results of mFISH using all 21 murine whole chromosome paints as probes applied on murine MM cell line AB1 are shown here. b Typical pseudocolorbanding-results for murine multicolor banding (mcb) as applied on cell line AB1 for chromosomes 1 (mcb1), 2 (mcb2) and 6 (mcb6). Derivative chromosomes are shown as 1/2 a = der(1)t(1;2)(H5;F1), 1/2 b , = der(1)t(1;2)(C1;F1), 2/6 = der(2)(2A1→2H4::6F3~G1→6E1::6F3~G1→6qter) and 6/2 = der(6)t(2;6)(H1;E1); normal chromosomes are labeled by # and chromosome number

Article Snippet: The murine cell lines AB1 and AC29 were obtained from Cell Bank Australia (Westmead, Australia, order #s CBA-0144 and CBA-0152) and AB22 European Collection of Authenticated Cell Cultures (Salisbury, UK—order# ECACC 10092307).

Techniques: Labeling

Journal: Molecular Cytogenetics

Article Title: Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

doi: 10.1186/s13039-020-00511-4

Figure Lengend Snippet: aCGH results for cell line AB1. In a copy number variations detected are summarized with respect to a tetraploid karyotype. Gains are depicted as green bars (one more copy = light green; two more copies = dark green), loss of one copy is depicted as a red bar and loss of two copies is depicted as a dark-red bar. Breaks are registered here as arrows. In b results of in silico translation for AB1 to human genome are shown the same way as in a

Article Snippet: The murine cell lines AB1 and AC29 were obtained from Cell Bank Australia (Westmead, Australia, order #s CBA-0144 and CBA-0152) and AB22 European Collection of Authenticated Cell Cultures (Salisbury, UK—order# ECACC 10092307).

Techniques: In Silico

Journal: Molecular Cytogenetics

Article Title: Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

doi: 10.1186/s13039-020-00511-4

Figure Lengend Snippet: Comparison of ‘translated’ imbalances of murine MM-cellines AB1, AB22 and AC29 with human epitheloid, biphasic and sarcomatoid MM, according to Krismann et al. [ 22 ]

Article Snippet: The murine cell lines AB1 and AC29 were obtained from Cell Bank Australia (Westmead, Australia, order #s CBA-0144 and CBA-0152) and AB22 European Collection of Authenticated Cell Cultures (Salisbury, UK—order# ECACC 10092307).

Techniques: Comparison

Journal: Molecular Cytogenetics

Article Title: Cytogenomic characterization of three murine malignant mesothelioma tumor cell lines

doi: 10.1186/s13039-020-00511-4

Figure Lengend Snippet: The four tumor suppressor genes most often involved in human MM acc. to [ 7 – 16 ], being deleted and/or mutated there are compared for copy number variant observed in the three studied cell lines

Article Snippet: The murine cell lines AB1 and AC29 were obtained from Cell Bank Australia (Westmead, Australia, order #s CBA-0144 and CBA-0152) and AB22 European Collection of Authenticated Cell Cultures (Salisbury, UK—order# ECACC 10092307).

Techniques: Variant Assay

Journal: Scientific Reports

Article Title: Topological insulator bismuth selenide as a theranostic platform for simultaneous cancer imaging and therapy

doi: 10.1038/srep01998

Figure Lengend Snippet: (a) Cell viability of H22 cells after incubation with increased concentration of Bi 2 Se 3 nanoplates. (b) ICP-MS results of H22 cells incubated with Bi 2 Se 3 nanoplates at 37°C and 4°C. Error bars correspond to mean ± standard deviations.

Article Snippet: Murine hepatocarcinoma cell line H22 was purchased from China Centre for Type Culture Collection (CCTCC, Wuhan, China), and cultured according to the guidelines given.

Techniques: Incubation, Concentration Assay

Journal: Scientific Reports

Article Title: Topological insulator bismuth selenide as a theranostic platform for simultaneous cancer imaging and therapy

doi: 10.1038/srep01998

Figure Lengend Snippet: (a) In vitro CT images of Bi 2 Se 3 nanoplates and Iopamidol with different concentrations. Cell analysis: H22 cells incubated without contrast agent (1), with increased concentration of Bi 2 Se 3 nanoplates (0.02 and 0.05 mol Bi l -1 for 2 and 3, respectively). (b) CT value (HU) of Bi 2 Se 3 nanoplates ( ) or Iopamidol ( ) as function of the concentration. (c) CT coronal views of a mouse following an intratumoral injection of 100 μl of Bi 2 Se 3 nanoplates solution (0.2 mol Bi l −1 ) (top). The corresponding 3D rendering of in vivo CT images above (bottom). The position of tumor is marked by red circles.

Article Snippet: Murine hepatocarcinoma cell line H22 was purchased from China Centre for Type Culture Collection (CCTCC, Wuhan, China), and cultured according to the guidelines given.

Techniques: In Vitro, Cell Analysis, Incubation, Concentration Assay, Injection, In Vivo

Journal: Scientific Reports

Article Title: Topological insulator bismuth selenide as a theranostic platform for simultaneous cancer imaging and therapy

doi: 10.1038/srep01998

Figure Lengend Snippet: (a) Photothermal effect of pure water and Bi 2 Se 3 nanoplates with different concentrations (a–e: 0, 5, 10, 20, 50 μg ml −1 ) upon the irradiation of 1 W cm −2 808 nm laser. (b) H22 cell viabilities cultured with Bi 2 Se 3 nanoplates at different concentrations with or without laser irradiation. (c) Growth of H22 tumors in different groups of mice after treatment. The relative tumor volumes were normalized to their initial sizes. (d) Representative photos of a Bi 2 Se 3 nanoplates-injected mouse at day 0 before PTT treatment and at day 20 after treatment. Error bars correspond to mean ± standard deviations.

Article Snippet: Murine hepatocarcinoma cell line H22 was purchased from China Centre for Type Culture Collection (CCTCC, Wuhan, China), and cultured according to the guidelines given.

Techniques: Irradiation, Cell Culture, Injection

Journal: Frontiers in Veterinary Science

Article Title: Detection of bimodal survivin expressions in canine cancer types by flow cytometry compared to immunohistochemistry

doi: 10.3389/fvets.2025.1552415

Figure Lengend Snippet: Analysis of survivin expression sites by IHC and WB. (A) Images of HE staining and survivin expression via IHC in canine melanoma cell lines (CMM2, CMeC, and LMeC) are shown. (B) Images of HE staining and survivin expression via IHC in murine cell lines (p815, CT26, and B16F10) are shown. (C) The cytosol and total survivin expression patterns via WB are indicated. (D) The expression levels of total survivin (blue bar) and cytosolic survivin (orange bar) corrected on the basis of β-actin expression are shown via density of plot analysis via ImageJ software.

Article Snippet: A total of six cell lines were used: canine malignant melanoma lines [CMM2, CMeC2, LMeC; provided by Dr. Takayuki Nakagawa, Department of Veterinary Surgery, University of Tokyo; ( )], the murine malignant melanoma line B16F10, the murine mast cell tumor line p815, and the murine colon cancer line CT26 (distributed for a fee by the JCRB Cell Bank).

Techniques: Expressing, Staining, Software

Journal: Materials Today Bio

Article Title: Neutrophil membrane-mimicking nanodecoys with intrinsic anti-inflammatory properties alleviate sepsis-induced acute liver injury and lethality in a mouse endotoxemia model

doi: 10.1016/j.mtbio.2022.100244

Figure Lengend Snippet: Effects of neutrophil membrane-mimicking nanodecoys (NM) and red cell membrane-mimicking nanovesicles (RM) on the LPS-induced cytotoxicity (A), lactate dehydrogenase (LDH) release (B), nitric oxide (NO) secretion (C), CXC-Chemokine Ligand 2 (CXCL2) expression (D), Reactive Oxygen Species (ROS) generation indicated by fluorescence intensity (E), and Cyclooxygenase-2 (COX-2) expression ( Fig. 8 F–H) in NCTC1469 murine liver cells; Scale bars, 50 ​μm; & p ​< ​0.05 compared with the CK group; ∗ p ​< ​0.05 compared with the LPS ​+ ​PBS group; # p ​< ​0.05 compared with the LPS ​+ ​NM group. Statistical differences between groups were performed by a one-way ANOVA for Fig. 8 A, B, C, E, and F. Statistical differences between groups were performed by SNK multiple range test for Fig. 8 D. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: The NCTC1469 murine liver cells and C166 mouse endothelial cells were obtained from China Center for Type Culture Collection and cultured in a DMEM medium (Life Technologies, CA, USA) supplemented with 10% FBS (Life Technologies, CA, USA) and 1% penicillin-streptomycin solution (Thermo Fisher Scientific, MA, USA) at 37 °C in a humidified atmosphere of 5% CO 2 .

Techniques: Membrane, Expressing, Fluorescence