the filter sets dapi and alexa fluor 594 Search Results


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Danaher Inc dapi staining
( A ) Morphological analysis of LS174T clones. The figure shows a small cell size clone (C3) and a large cell size clone (C5) stained with phalloidin (red, cytoskeleton) and <t>DAPI</t> (blue, nuclei). Pictures were taken at 200× magnification. Scale bar 50 μm is shown in the bottom right corner of the pictures. ( B ) Nuclei area of LS174T and derived clones, measured <t>by</t> <t>microscopy</t> after DAPI staining. The parental cell line (CL) in green. Clones are colored according to the average nuclei size into small (blue) and large (red) and classified by unsupervised clustering based on the difference of their average nuclei size (dendrogram on the left). ( C ) Percentage of nuclei with areas larger than 115 μm 2 in LS174T and derived clones. Most of the clones exhibited a low proportion (less than 10%, low group, blue) of nuclei above 115 μm 2 . The parental cell line (CL) and clones C9 and C12 exhibited a larger proportion (10~25%, mid group, in purple). Clones C5–C8 exhibited around 50% of nuclei larger than that value (high group, in red).
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( A ) Morphological analysis of LS174T clones. The figure shows a small cell size clone (C3) and a large cell size clone (C5) stained with phalloidin (red, cytoskeleton) and <t>DAPI</t> (blue, nuclei). Pictures were taken at 200× magnification. Scale bar 50 μm is shown in the bottom right corner of the pictures. ( B ) Nuclei area of LS174T and derived clones, measured <t>by</t> <t>microscopy</t> after DAPI staining. The parental cell line (CL) in green. Clones are colored according to the average nuclei size into small (blue) and large (red) and classified by unsupervised clustering based on the difference of their average nuclei size (dendrogram on the left). ( C ) Percentage of nuclei with areas larger than 115 μm 2 in LS174T and derived clones. Most of the clones exhibited a low proportion (less than 10%, low group, blue) of nuclei above 115 μm 2 . The parental cell line (CL) and clones C9 and C12 exhibited a larger proportion (10~25%, mid group, in purple). Clones C5–C8 exhibited around 50% of nuclei larger than that value (high group, in red).
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Cell Signaling Technology Inc antibody antirabbit igg h l alexa fluor 594 conjugate cell signaling
( A ) Morphological analysis of LS174T clones. The figure shows a small cell size clone (C3) and a large cell size clone (C5) stained with phalloidin (red, cytoskeleton) and <t>DAPI</t> (blue, nuclei). Pictures were taken at 200× magnification. Scale bar 50 μm is shown in the bottom right corner of the pictures. ( B ) Nuclei area of LS174T and derived clones, measured <t>by</t> <t>microscopy</t> after DAPI staining. The parental cell line (CL) in green. Clones are colored according to the average nuclei size into small (blue) and large (red) and classified by unsupervised clustering based on the difference of their average nuclei size (dendrogram on the left). ( C ) Percentage of nuclei with areas larger than 115 μm 2 in LS174T and derived clones. Most of the clones exhibited a low proportion (less than 10%, low group, blue) of nuclei above 115 μm 2 . The parental cell line (CL) and clones C9 and C12 exhibited a larger proportion (10~25%, mid group, in purple). Clones C5–C8 exhibited around 50% of nuclei larger than that value (high group, in red).
Antibody Antirabbit Igg H L Alexa Fluor 594 Conjugate Cell Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


( A ) Morphological analysis of LS174T clones. The figure shows a small cell size clone (C3) and a large cell size clone (C5) stained with phalloidin (red, cytoskeleton) and DAPI (blue, nuclei). Pictures were taken at 200× magnification. Scale bar 50 μm is shown in the bottom right corner of the pictures. ( B ) Nuclei area of LS174T and derived clones, measured by microscopy after DAPI staining. The parental cell line (CL) in green. Clones are colored according to the average nuclei size into small (blue) and large (red) and classified by unsupervised clustering based on the difference of their average nuclei size (dendrogram on the left). ( C ) Percentage of nuclei with areas larger than 115 μm 2 in LS174T and derived clones. Most of the clones exhibited a low proportion (less than 10%, low group, blue) of nuclei above 115 μm 2 . The parental cell line (CL) and clones C9 and C12 exhibited a larger proportion (10~25%, mid group, in purple). Clones C5–C8 exhibited around 50% of nuclei larger than that value (high group, in red).

Journal: Cancers

Article Title: Somatic Hypomethylation of Pericentromeric SST1 Repeats and Tetraploidization in Human Colorectal Cancer Cells

doi: 10.3390/cancers13215353

Figure Lengend Snippet: ( A ) Morphological analysis of LS174T clones. The figure shows a small cell size clone (C3) and a large cell size clone (C5) stained with phalloidin (red, cytoskeleton) and DAPI (blue, nuclei). Pictures were taken at 200× magnification. Scale bar 50 μm is shown in the bottom right corner of the pictures. ( B ) Nuclei area of LS174T and derived clones, measured by microscopy after DAPI staining. The parental cell line (CL) in green. Clones are colored according to the average nuclei size into small (blue) and large (red) and classified by unsupervised clustering based on the difference of their average nuclei size (dendrogram on the left). ( C ) Percentage of nuclei with areas larger than 115 μm 2 in LS174T and derived clones. Most of the clones exhibited a low proportion (less than 10%, low group, blue) of nuclei above 115 μm 2 . The parental cell line (CL) and clones C9 and C12 exhibited a larger proportion (10~25%, mid group, in purple). Clones C5–C8 exhibited around 50% of nuclei larger than that value (high group, in red).

Article Snippet: Cell morphology was studied by fluorescence microscopy after phalloidin and DAPI staining (Phalloidin-iFluor 594 Reagent, ab176757—Abcam).

Techniques: Clone Assay, Staining, Derivative Assay, Microscopy