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CLS Cell Lines Service GmbH
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AMS Biotechnology
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BioResource International Inc
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Johns Hopkins HealthCare
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Korean Cell Line Bank
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iCell Bioscience Inc
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ScienCell
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Keygen Biotech
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JCRB Cell Bank
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STEMCELL Technologies Inc
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Dainippon Sumitomo
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European Collection of Authenticated Cell Cultures
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Image Search Results
Journal: mAbs
Article Title: Generation and in vivo characterization of a novel high-affinity human antibody targeting carcinoembryonic antigen
doi: 10.1080/19420862.2023.2217964
Figure Lengend Snippet: In vitro characterization of new anti-CEA antibodies. (a) SPR sensorgram of G9, F7, and F4 in a scFv format. K D values were calculated to be 640 nM, 50 nM, and 7.7 nM, respectively. (b) Flow cytometry analysis with the new antibodies in IgG format on CEA-expressing CT26 cells and on CEA-negative CT26 wild-type cells. (c) Immunofluorescence staining with IgG formats on the human colon adenocarcinoma xenograft LS174T. Anti-CEA antibodies were detected in green. Blood vessels were detected by CD31 staining (red). 20× magnification, scale bars = 100 μm.
Article Snippet: Immunofluorescence analysis was performed on
Techniques: In Vitro, Flow Cytometry, Expressing, Immunofluorescence, Staining
Journal: mAbs
Article Title: Generation and in vivo characterization of a novel high-affinity human antibody targeting carcinoembryonic antigen
doi: 10.1080/19420862.2023.2217964
Figure Lengend Snippet: Ex vivo immunofluorescence-based biodistribution analysis. Immunofluorescence analysis assessed tumor targeting of new anti-CEA antibodies in IgG format. Two hundred micrograms of IgG-FITC were injected intravenously into LS174T-bearing mice. Tumors were excised 24 hours after injection. IgG-FITC was detected in green; blood vessels were detected through CD31 staining (red). 20× magnification, scale bars = 100 μm.
Article Snippet: Immunofluorescence analysis was performed on
Techniques: Ex Vivo, Immunofluorescence, Injection, Staining
Journal: mAbs
Article Title: Generation and in vivo characterization of a novel high-affinity human antibody targeting carcinoembryonic antigen
doi: 10.1080/19420862.2023.2217964
Figure Lengend Snippet: Quantitative biodistribution with radiolabeled anti-CEA antibodies in diabody format. Quantitative biodistribution analysis of radio iodinated anti-CEA diabodies in BALB/c nude mice bearing subcutaneous LS174T colon adenocarcinomas. Organs were harvested 24 hours after intravenous injection, and radioactivity was quantified. Results are shown as the percentage of injected dose per gram (ID/g (%)). Error bars = SEM; n = 4.
Article Snippet: Immunofluorescence analysis was performed on
Techniques: Injection, Radioactivity
Journal: International Journal of Molecular Sciences
Article Title: Novel Lipid Nanocomplex Co-Carrying Bcl2 siRNA and Quantum Dots for EGF Receptor-Targeted Anti-Cancer Theranosis
doi: 10.3390/ijms25116246
Figure Lengend Snippet: Tumor-targeted siRNA delivery of QDM and immuno-QDM. Protein expression of MDA-MB-453 (EGFR negative) and LS174T (EGFR positive) cells, and the target tumor cell binding and cellular uptake assay of Chol-siRNA, QDM, and immuno-QDM ( A – C ) were evaluated. All particles were incubated with the target cells (LS174T) for 1 h and 8 h at 37 °C and analyzed with a confocal microscope for evaluate siRNA delivery and endosomal escape analysis of QDM and immuno-QDM ( D ) (X400).
Article Snippet: The
Techniques: Expressing, Binding Assay, Incubation, Microscopy
Journal: International Journal of Molecular Sciences
Article Title: Novel Lipid Nanocomplex Co-Carrying Bcl2 siRNA and Quantum Dots for EGF Receptor-Targeted Anti-Cancer Theranosis
doi: 10.3390/ijms25116246
Figure Lengend Snippet: Knockdown of target gene and in vitro anti-cancer efficacy of QDM/siBcl2 and iQDM/siBcl2. ( A , B ) The bcl2 gene knockdown was detected with PCR and Western blot (25, 50 pm). ( C ) MTT assay results of LS174T and MDA-MB-453 cells after the treatment of siRNA, QDM/siBcl2, and iQDM/siBcl2.
Article Snippet: The
Techniques: Knockdown, In Vitro, Western Blot, MTT Assay
Journal: ACS Omega
Article Title: Microbubble Enhanced Delivery of Vitamin C for Treatment of Colorectal Cancer
doi: 10.1021/acsomega.4c06779
Figure Lengend Snippet: LS174TIn VitroCell Response to PAL. LS174T cell viability following 1 h exposure to PAL and BL. The bar chart shows treatment with PAL compared to the carrier (BL), which used the same liposome preparation method and yielded a similar liposome concentration but omitted PA ( n = 3, error bars represent standard error for three biological repeats).
Article Snippet:
Techniques: Concentration Assay
Journal: ACS Omega
Article Title: Microbubble Enhanced Delivery of Vitamin C for Treatment of Colorectal Cancer
doi: 10.1021/acsomega.4c06779
Figure Lengend Snippet: Fluorescence maps and analysis of LS174T cells cultured on-chip and treated with PAL, MBs, and US. Treatment with (a) culture media only, or (b) PAL + MB + US (5×). Histograms showing the distribution of live and dead stained cells (dead pixel count multiplied by 10 to aid visualization), corresponding to the confocal images of LS174T cells post-treatment with (c) culture media or (d) PAL + MB + US (5×). Histograms showing the distribution of the fraction of dead LS174T cells (dead pixel count/total pixel count) which received treatment with (e) culture media only or (f) PAL + MB + US (5×).
Article Snippet:
Techniques: Fluorescence, Cell Culture, Staining
Journal: ACS Omega
Article Title: Microbubble Enhanced Delivery of Vitamin C for Treatment of Colorectal Cancer
doi: 10.1021/acsomega.4c06779
Figure Lengend Snippet: LS174T cell viability post BL, PAL, MB, and US exposures on-chip. (a) Cell viability data for LS174T cells on-chip, post-treatment with BL, PAL (5 mM), MB (1 × 10 8 MBs/mL), and US combinations ( n > 3 for all conditions, except for PAL (No US), conducted twice; error bars represent the standard error). Confocal images of stained LS174T cells following treatment with PAL + MB + US (5×) (b) inside and (c) outside of the US-exposed region. Confocal images of stained LS174T cells treated with culture media (DMEM) in the channel’s (d) central and (e) edge regions.
Article Snippet:
Techniques: Staining