Review




Structured Review

MetaCell Inc ctc kit
Qualitative assessment of MetaCell’s ability to retain CRC cells spiked into blood. After filtration, the cells retained on <t>the</t> <t>MetaCell</t> membrane from the following samples were stained with Hoechst 33,342 (nuclear stain), white blood cell (WBC) markers (CD45 and CD16), and <t>CTC</t> markers (EpCAM and cytokeratins): unspiked healthy blood (negative control, top row), healthy blood spiked with CRC cells (middle row), and unfiltered CRC cells (positive control, bottom row). The representative images show that unspiked healthy blood cells retained after filtering were positive for WBC markers and lacking CTC markers. Both healthy blood spiked with CRC cells retained on the MetaCell membrane and unfiltered CRC cells were positive for Hoechst 33,342 and CTC markers but negative for WBC markers. Cells were visualised on a Nikon A1+ confocal microscope at 200× magnification. Scale bar represents 80 µm.
Ctc Kit, supplied by MetaCell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Images

1) Product Images from "Assessment of a Size-Based Method for Enriching Circulating Tumour Cells in Colorectal Cancer"

Article Title: Assessment of a Size-Based Method for Enriching Circulating Tumour Cells in Colorectal Cancer

Journal: Cancers

doi: 10.3390/cancers14143446

Qualitative assessment of MetaCell’s ability to retain CRC cells spiked into blood. After filtration, the cells retained on the MetaCell membrane from the following samples were stained with Hoechst 33,342 (nuclear stain), white blood cell (WBC) markers (CD45 and CD16), and CTC markers (EpCAM and cytokeratins): unspiked healthy blood (negative control, top row), healthy blood spiked with CRC cells (middle row), and unfiltered CRC cells (positive control, bottom row). The representative images show that unspiked healthy blood cells retained after filtering were positive for WBC markers and lacking CTC markers. Both healthy blood spiked with CRC cells retained on the MetaCell membrane and unfiltered CRC cells were positive for Hoechst 33,342 and CTC markers but negative for WBC markers. Cells were visualised on a Nikon A1+ confocal microscope at 200× magnification. Scale bar represents 80 µm.
Figure Legend Snippet: Qualitative assessment of MetaCell’s ability to retain CRC cells spiked into blood. After filtration, the cells retained on the MetaCell membrane from the following samples were stained with Hoechst 33,342 (nuclear stain), white blood cell (WBC) markers (CD45 and CD16), and CTC markers (EpCAM and cytokeratins): unspiked healthy blood (negative control, top row), healthy blood spiked with CRC cells (middle row), and unfiltered CRC cells (positive control, bottom row). The representative images show that unspiked healthy blood cells retained after filtering were positive for WBC markers and lacking CTC markers. Both healthy blood spiked with CRC cells retained on the MetaCell membrane and unfiltered CRC cells were positive for Hoechst 33,342 and CTC markers but negative for WBC markers. Cells were visualised on a Nikon A1+ confocal microscope at 200× magnification. Scale bar represents 80 µm.

Techniques Used: Filtration, Staining, Negative Control, Positive Control, Microscopy

Quantitative analysis of CTC markers in unfiltered and MetaCell-filtered CRC cells. ( A ) Expression of CTC markers ( EPCAM and KRT20 ) for unfiltered (HCT116_UF) and MetaCell-filtered HCT116 cells (HCT116_MF). ( B ) Expression of CTC markers for unfiltered DLD1 cells (DLD1_UF) and MetaCell-filtered DLD1 cells (DLD1_MF). Error bars represent the mean ± SD of three biological replicates. p -values determined by paired Student’s t -test; ns p > 0.05.
Figure Legend Snippet: Quantitative analysis of CTC markers in unfiltered and MetaCell-filtered CRC cells. ( A ) Expression of CTC markers ( EPCAM and KRT20 ) for unfiltered (HCT116_UF) and MetaCell-filtered HCT116 cells (HCT116_MF). ( B ) Expression of CTC markers for unfiltered DLD1 cells (DLD1_UF) and MetaCell-filtered DLD1 cells (DLD1_MF). Error bars represent the mean ± SD of three biological replicates. p -values determined by paired Student’s t -test; ns p > 0.05.

Techniques Used: Expressing

MetaCell recovery rates for healthy blood spiked with different concentrations of CRC cells. Different numbers (10, 100, and 500) of either HCT116 cells ( A ) or DLD1 cells ( B ) were spiked into healthy blood samples and filtered with MetaCell. The cells retained on the membrane and the same number of unfiltered cells were immunostained with CTC (EpCAM or cytokeratins) and WBC markers (CD45 and CD16). Cells that stained positively for Hoechst 33,342 and and at least one of the CTC markers but did not stain for WBC markers were manually counted using a Nikon A1+ confocal microscope at 200× magnification. Recovery rates are represented as the mean ± SD of three biological replicates. p -values were determined by a paired t -test. ns p > 0.05.
Figure Legend Snippet: MetaCell recovery rates for healthy blood spiked with different concentrations of CRC cells. Different numbers (10, 100, and 500) of either HCT116 cells ( A ) or DLD1 cells ( B ) were spiked into healthy blood samples and filtered with MetaCell. The cells retained on the membrane and the same number of unfiltered cells were immunostained with CTC (EpCAM or cytokeratins) and WBC markers (CD45 and CD16). Cells that stained positively for Hoechst 33,342 and and at least one of the CTC markers but did not stain for WBC markers were manually counted using a Nikon A1+ confocal microscope at 200× magnification. Recovery rates are represented as the mean ± SD of three biological replicates. p -values were determined by a paired t -test. ns p > 0.05.

Techniques Used: Staining, Microscopy

Gene expression analysis to evaluate the effect of cell numbers on the recovery rates for MetaCell. The gene expression analysis of CTC markers ( EpCAM and KRT20 ) for the different numbers of unfiltered (10, 100, and 500 UF) and MetaCell-filtered HCT116 ( A ) or DLD1 ( B ) cells (10, 100, and 500 MF). Error bars represent the mean ± SD of three biological replicates. p -values were determined by paired t -tests. ns p > 0.05 for both cell lines.
Figure Legend Snippet: Gene expression analysis to evaluate the effect of cell numbers on the recovery rates for MetaCell. The gene expression analysis of CTC markers ( EpCAM and KRT20 ) for the different numbers of unfiltered (10, 100, and 500 UF) and MetaCell-filtered HCT116 ( A ) or DLD1 ( B ) cells (10, 100, and 500 MF). Error bars represent the mean ± SD of three biological replicates. p -values were determined by paired t -tests. ns p > 0.05 for both cell lines.

Techniques Used: Expressing



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Image Search Results


(A) Representative immunofluorescence images of CTCs with different extraction methods. Co-localization of STING (green, Alexa Fluor 488) and vimentin (red, Alexa Fluor 647). Nuclei were stained with DAPI (blue). Magnification 63X. (B) Representative SEM images of the isolated exosomes (scale bar = 2 μm). (C) Western blot of exosomal markers CD81 and CD63. The isolated exosomes with different protein concentrations (EXO#1 = 40 μg and EXO#2 = 20 μg) were successfully obtained from the culture supernatants of PBMCs from SCLC patients. Red line indicated the band of each protein on the gel. Original western blots are presented in File S1. (D) Stacked bar plots showing the log10-transformed positive control read counts across the samples. (E) Violin plot displaying the distribution of the log of the un-normalized gene counts for all the samples.

Journal: The Journal of Liquid Biopsy

Article Title: Novel applications of liquid Biopsy: Comprehensive methodology for circulating biomarker exploration in peripheral blood

doi: 10.1016/j.jlb.2025.100307

Figure Lengend Snippet: (A) Representative immunofluorescence images of CTCs with different extraction methods. Co-localization of STING (green, Alexa Fluor 488) and vimentin (red, Alexa Fluor 647). Nuclei were stained with DAPI (blue). Magnification 63X. (B) Representative SEM images of the isolated exosomes (scale bar = 2 μm). (C) Western blot of exosomal markers CD81 and CD63. The isolated exosomes with different protein concentrations (EXO#1 = 40 μg and EXO#2 = 20 μg) were successfully obtained from the culture supernatants of PBMCs from SCLC patients. Red line indicated the band of each protein on the gel. Original western blots are presented in File S1. (D) Stacked bar plots showing the log10-transformed positive control read counts across the samples. (E) Violin plot displaying the distribution of the log of the un-normalized gene counts for all the samples.

Article Snippet: MACS® Tumor Cell Isolation Kit depletes tumor-associated cells without harming CTCs; we modified the protocol by omitting Non-Tumor Cell Depletion Cocktail B to preserve mesenchymal CTCs (Order no. 130-108-339, www.miltenyibiotec.com ).

Techniques: Immunofluorescence, Extraction, Staining, Isolation, Western Blot, Transformation Assay, Positive Control