dapi (Beyotime)
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Dapi, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 32584 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 32584 article reviews
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Staining:Article Title: Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination Article Snippet: .. Cell staining and viability assays were performed using a LIVE/DEAD kit (calcein AM/propidium iodide), an annexin V–FITC/PI apoptosis detection kit, MTT reagent, Alexa Fluor 488–conjugated secondary antibody, and Article Title: CD52+ cells are associated with faster short-term neutrophil recovery in mobilized hematopoietic stem cell transplant. Article Snippet: .. Cells were stained with CD52 primary antibody (Bioss, #bs-34117R) at 4 oC for overnight, and subsequently incubated for 2 hours at 37 oC with the Alexa Flur 488- conjugated anti-rabbit secondary antibody (Invitrogen, #A21206) and Article Title: DEAD-box RNA helicase 21 interacts with the nucleocapsid protein and inhibits porcine deltacoronavirus infection through upregulation of interferon responses. Article Snippet: The cells were then incubated with primary antibodies for 1 h, followed by washing with PBS and incubation with Alexa Fluor 488- and 594-conjugated secondary antibodies (Thermo Fisher Scientific) for 1 h at 37°C in the dark. .. Afterward, the cells were stained with MTT Assay:Article Title: Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination Article Snippet: .. Cell staining and viability assays were performed using a LIVE/DEAD kit (calcein AM/propidium iodide), an annexin V–FITC/PI apoptosis detection kit, MTT reagent, Alexa Fluor 488–conjugated secondary antibody, and Incubation:Article Title: CD52+ cells are associated with faster short-term neutrophil recovery in mobilized hematopoietic stem cell transplant. Article Snippet: .. Cells were stained with CD52 primary antibody (Bioss, #bs-34117R) at 4 oC for overnight, and subsequently incubated for 2 hours at 37 oC with the Alexa Flur 488- conjugated anti-rabbit secondary antibody (Invitrogen, #A21206) and Article Title: Glucocorticoid-induced METTL3 promotes SONFH by enhancing MEG3 m6A methylation and subsequent ABL2 upregulation. Article Snippet: Background: Steroid-induced osteonecrosis of the femoral head (SONFH) is a refractory orthopedic disease.. While N6-methyladenosine (m6A) modification is implicated in bone metabolism, its specific role and mechanism in SONFH pathogenesis require further elucidation.. Methods: Bioinformatics analysis identified key m6A-related genes. Confocal:Article Title: DEAD-box RNA helicase 21 interacts with the nucleocapsid protein and inhibits porcine deltacoronavirus infection through upregulation of interferon responses. Article Snippet: The cells were then incubated with primary antibodies for 1 h, followed by washing with PBS and incubation with Alexa Fluor 488- and 594-conjugated secondary antibodies (Thermo Fisher Scientific) for 1 h at 37°C in the dark. .. Afterward, the cells were stained with Microscopy:Article Title: DEAD-box RNA helicase 21 interacts with the nucleocapsid protein and inhibits porcine deltacoronavirus infection through upregulation of interferon responses. Article Snippet: The cells were then incubated with primary antibodies for 1 h, followed by washing with PBS and incubation with Alexa Fluor 488- and 594-conjugated secondary antibodies (Thermo Fisher Scientific) for 1 h at 37°C in the dark. .. Afterward, the cells were stained with TUNEL Assay:Article Title: Glucocorticoid-induced METTL3 promotes SONFH by enhancing MEG3 m6A methylation and subsequent ABL2 upregulation. Article Snippet: Background: Steroid-induced osteonecrosis of the femoral head (SONFH) is a refractory orthopedic disease.. While N6-methyladenosine (m6A) modification is implicated in bone metabolism, its specific role and mechanism in SONFH pathogenesis require further elucidation.. Methods: Bioinformatics analysis identified key m6A-related genes. |
![Combining fluorescence microscopy with multiplex IMC data of colorectal tissue advances quality of single cell segmentation. a Cartoon describing MATISSE, a novel pipeline adding microscopic imaging to multiplex IMC analysis and downstream segmentation. In short: tissue sections on slides were stained using isotope-conjugated primary antibodies, DNA intercalator, and <t>DAPI.</t> The tissue was first scanned using <t>a</t> <t>fluorescent</t> microscope and then processed with IMC. Data produced by both techniques is aligned using the nuclear staining. Nuclear and membranous pixel probability maps are produced based on the fluorescent images and IMC data respectively. These probability maps are used to generate a segmentation map, where all detected cells are included. b Representative images of DNA intercalator on a colorectal tissue section analyzed by Ir193 labeling and IMC (left) or DAPI labeling and fluorescent microscopy (IF, right). c IMC-only (IMC) and MATISSE cell segmentation (MATISSE) were performed, and shown are the different predicted outlines on a representative image of Ir193 labeling. Arrows indicate areas with cell fragmentation. d Display of a large region of interest (ROI) showing an overlay of the predicted cell outlines (pink) upon IMC or MATISSE segmentation on a representative IMC image of DNA-Ir193 labeling of colorectal tissue. Highlighted in yellow is the approximate position of the basement membrane surrounding the epithelial monolayer. Scale bar 25 μm. e Cell density was calculated as the number of cells within a radius of 10 μM from the center of each single cell [ , ]. This number is displayed with a color code for each cell in the representative image](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_4487/pmc08114487/pmc08114487__12915_2021_1043_Fig1_HTML.jpg)