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fluorochrome conjugated antibodies against fitc cd45  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology fluorochrome conjugated antibodies against fitc cd45
    Fluorochrome Conjugated Antibodies Against Fitc Cd45, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fluorochrome conjugated antibodies against fitc cd45/product/Elabscience Biotechnology
    Average 94 stars, based on 5 article reviews
    fluorochrome conjugated antibodies against fitc cd45 - by Bioz Stars, 2026-06
    94/100 stars

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    Cell and extracellular matrix (ECM) composition of mCSs formed in ULA U-well plates and PDL-coated plates. ( a , b ): Images of mCSs stained by endothelial cell (EC) marker (CD31, red), progenitor cell markers (c-Kit, red; Sca-1, red; Oct4, red), smooth-muscle cell marker (SMA, green), mesenchymal markers (CD105, red; <t>CD90,</t> green; CD73, green), and ECM proteins (COL I, green; FN, green). Nuclei were stained with DAPI. Yellow arrows indicate positive staining. ( c ) Bar plot of a positive staining cell fraction per nuclei within the mCS slice, n = 3, * p < 0.05. ( d ) Bar plot of fluorescence intensity signal normalized per mCS slice area, n = 3, ** p < 0.01. SMA—smooth muscle actin, COL I—collagen type I, FN—fibronectin.
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    Image Search Results


    Cell and extracellular matrix (ECM) composition of mCSs formed in ULA U-well plates and PDL-coated plates. ( a , b ): Images of mCSs stained by endothelial cell (EC) marker (CD31, red), progenitor cell markers (c-Kit, red; Sca-1, red; Oct4, red), smooth-muscle cell marker (SMA, green), mesenchymal markers (CD105, red; CD90, green; CD73, green), and ECM proteins (COL I, green; FN, green). Nuclei were stained with DAPI. Yellow arrows indicate positive staining. ( c ) Bar plot of a positive staining cell fraction per nuclei within the mCS slice, n = 3, * p < 0.05. ( d ) Bar plot of fluorescence intensity signal normalized per mCS slice area, n = 3, ** p < 0.01. SMA—smooth muscle actin, COL I—collagen type I, FN—fibronectin.

    Journal: International Journal of Molecular Sciences

    Article Title: The 3D World of Spheroids: Searching for an Optimal Method of Fabricating Pro-Reparative Cardiospheres

    doi: 10.3390/ijms262412025

    Figure Lengend Snippet: Cell and extracellular matrix (ECM) composition of mCSs formed in ULA U-well plates and PDL-coated plates. ( a , b ): Images of mCSs stained by endothelial cell (EC) marker (CD31, red), progenitor cell markers (c-Kit, red; Sca-1, red; Oct4, red), smooth-muscle cell marker (SMA, green), mesenchymal markers (CD105, red; CD90, green; CD73, green), and ECM proteins (COL I, green; FN, green). Nuclei were stained with DAPI. Yellow arrows indicate positive staining. ( c ) Bar plot of a positive staining cell fraction per nuclei within the mCS slice, n = 3, * p < 0.05. ( d ) Bar plot of fluorescence intensity signal normalized per mCS slice area, n = 3, ** p < 0.01. SMA—smooth muscle actin, COL I—collagen type I, FN—fibronectin.

    Article Snippet: The EDCs were trypsinized, washed in ice-cold FASC buffer (5% FBS, 0.1% sodium azide in Ca 2+ , Mg 2+ -free DPBS), and incubated with primary antibodies to CD105 (#120404, Biolegend, San Diego, CA, USA), Sca-1 conjugated with PE/Cy7 (E-AB-F1191UH, Elabscience, Wuhan, China), CD90 conjugated with FITC (E-AB-F1283UC, Elabscience), CD31 (#553370; BD, San Diego, CA, USA), and CD45 conjugated with PE (E-AB-F1136UD, Elabscience) or with isotype IgGs for 30 min on ice.

    Techniques: Staining, Marker, Fluorescence

    A Flow cytometry was used to detect CD34 + CD90 + ECs in 2 GBC tissues (PE: CD34, FITC: CD90). B Representative multiple immune staining images of CD34 and CD90 in GBC tissues. C Immune staining of CD34 and CD90 on GBC tissue microarray. D Analysis of the correlation between CD34 + or CD34 + CD90 + cell contents and patient survival prognosis and clinical characteristics. OS, overall survival time.

    Journal: NPJ Precision Oncology

    Article Title: Single-cell analysis reveals CD34 + CD90 + endothelial cells promote tumor metastasis in gallbladder cancer

    doi: 10.1038/s41698-025-01040-2

    Figure Lengend Snippet: A Flow cytometry was used to detect CD34 + CD90 + ECs in 2 GBC tissues (PE: CD34, FITC: CD90). B Representative multiple immune staining images of CD34 and CD90 in GBC tissues. C Immune staining of CD34 and CD90 on GBC tissue microarray. D Analysis of the correlation between CD34 + or CD34 + CD90 + cell contents and patient survival prognosis and clinical characteristics. OS, overall survival time.

    Article Snippet: Subsequently, FITC-conjugated CD90 antibody was added to the sorted CD34 + endothelial cells, and an EasySepTM Release Human FITC Positive Selection Kit (STEMCELL Technologies) was used to isolate CD34 + CD90 + endothelial cells.

    Techniques: Flow Cytometry, Staining, Microarray

    A Graphic flow chart showing of isolation process for CD34 + CD90 - and CD34 + CD90 + cells from GBC tissues using magnetic bead sorting. B Identify the purity of CD34 + CD90 + ECs before and after sorting by flow cytometry. C Representative images showing the morphology of primary CD34 + CD90 - (upper) and CD34 + CD90 + (lower) ECs. D The mRNA levels of mesenchymal transition-related genes were determined by qRT-PCR, a heatmap showing the relative ratios of CD34 + CD90 + /CD34 + CD90 - in 3 GBC samples. E Representative IF staining images showing the protein levels of CD34, CD90, and p-Smad2/3 in GBC tissue. F GBC-SD cells were co-cultured with isolated CD34 + CD90 + or CD34 + CD90 - cells. Representative images and quantification showing the effects of CD34 + CD90 + or CD34 + CD90 - cells on GBC-SD cell migration and invasion. G Transcriptional levels of mesenchymal transition-related genes MMP-9, FN-1, and TWIST in CD34 + CD90 + and CD34 + CD90 - cells with or without TGF-β pathway inhibitors (ITD, PFD) treatment were determined by qRT-PCR. H GBC-SD cells were co-cultured with isolated CD34 + CD90 + cells with or without MMP-9 antibodies and TGF-β pathway inhibitors (ITD, PFD) treatment. Representative images and quantification showing metastatic cell numbers in each group. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, ns, not significant.

    Journal: NPJ Precision Oncology

    Article Title: Single-cell analysis reveals CD34 + CD90 + endothelial cells promote tumor metastasis in gallbladder cancer

    doi: 10.1038/s41698-025-01040-2

    Figure Lengend Snippet: A Graphic flow chart showing of isolation process for CD34 + CD90 - and CD34 + CD90 + cells from GBC tissues using magnetic bead sorting. B Identify the purity of CD34 + CD90 + ECs before and after sorting by flow cytometry. C Representative images showing the morphology of primary CD34 + CD90 - (upper) and CD34 + CD90 + (lower) ECs. D The mRNA levels of mesenchymal transition-related genes were determined by qRT-PCR, a heatmap showing the relative ratios of CD34 + CD90 + /CD34 + CD90 - in 3 GBC samples. E Representative IF staining images showing the protein levels of CD34, CD90, and p-Smad2/3 in GBC tissue. F GBC-SD cells were co-cultured with isolated CD34 + CD90 + or CD34 + CD90 - cells. Representative images and quantification showing the effects of CD34 + CD90 + or CD34 + CD90 - cells on GBC-SD cell migration and invasion. G Transcriptional levels of mesenchymal transition-related genes MMP-9, FN-1, and TWIST in CD34 + CD90 + and CD34 + CD90 - cells with or without TGF-β pathway inhibitors (ITD, PFD) treatment were determined by qRT-PCR. H GBC-SD cells were co-cultured with isolated CD34 + CD90 + cells with or without MMP-9 antibodies and TGF-β pathway inhibitors (ITD, PFD) treatment. Representative images and quantification showing metastatic cell numbers in each group. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, ns, not significant.

    Article Snippet: Subsequently, FITC-conjugated CD90 antibody was added to the sorted CD34 + endothelial cells, and an EasySepTM Release Human FITC Positive Selection Kit (STEMCELL Technologies) was used to isolate CD34 + CD90 + endothelial cells.

    Techniques: Isolation, Flow Cytometry, Quantitative RT-PCR, Staining, Cell Culture, Migration

    A Workflow of in vivo liver metastasis experiment. B In vivo GBC-SD tumor growth ability was assessed using bioluminescence. C Identification of CD34 + CD90 + and CD34 + CD90 - cells in mouse liver tumor tissue by IF staining. D Representative images of mouse livers and H&E staining. E Representative images and quantification showing the IHC staining of MMP-9, FN1, and PDGFD in GBC-SD tumor-bearing mouse liver tissue. * P < 0.05, ** P < 0.01, *** P < 0.001, ns, not significant.

    Journal: NPJ Precision Oncology

    Article Title: Single-cell analysis reveals CD34 + CD90 + endothelial cells promote tumor metastasis in gallbladder cancer

    doi: 10.1038/s41698-025-01040-2

    Figure Lengend Snippet: A Workflow of in vivo liver metastasis experiment. B In vivo GBC-SD tumor growth ability was assessed using bioluminescence. C Identification of CD34 + CD90 + and CD34 + CD90 - cells in mouse liver tumor tissue by IF staining. D Representative images of mouse livers and H&E staining. E Representative images and quantification showing the IHC staining of MMP-9, FN1, and PDGFD in GBC-SD tumor-bearing mouse liver tissue. * P < 0.05, ** P < 0.01, *** P < 0.001, ns, not significant.

    Article Snippet: Subsequently, FITC-conjugated CD90 antibody was added to the sorted CD34 + endothelial cells, and an EasySepTM Release Human FITC Positive Selection Kit (STEMCELL Technologies) was used to isolate CD34 + CD90 + endothelial cells.

    Techniques: In Vivo, Staining, Immunohistochemistry

    A UMAP plot displaying major cell clusters and EC subclusters from single-cell data of GSE149614 . B Bubble plot showing expression levels of endothelial marker genes for each subset. C Heat maps showing Ro/e of endothelial subsets in non-tumor (N) and HCC tumor (T) tissues. D Bar chart displaying the distribution of each EC subset in non-tumor (N) and tumor (T) tissues. E Bubble plot and heatmap chart displaying the enriched pathways for each EC subset analyzed by GO. F Violin plots showing expression scores for extracellular matrix remodeling and angiogenesis-related genes for each EC subset. G Multiple IHC showing the CD34 + CD90 + ECs in HCC tumor tissue.

    Journal: NPJ Precision Oncology

    Article Title: Single-cell analysis reveals CD34 + CD90 + endothelial cells promote tumor metastasis in gallbladder cancer

    doi: 10.1038/s41698-025-01040-2

    Figure Lengend Snippet: A UMAP plot displaying major cell clusters and EC subclusters from single-cell data of GSE149614 . B Bubble plot showing expression levels of endothelial marker genes for each subset. C Heat maps showing Ro/e of endothelial subsets in non-tumor (N) and HCC tumor (T) tissues. D Bar chart displaying the distribution of each EC subset in non-tumor (N) and tumor (T) tissues. E Bubble plot and heatmap chart displaying the enriched pathways for each EC subset analyzed by GO. F Violin plots showing expression scores for extracellular matrix remodeling and angiogenesis-related genes for each EC subset. G Multiple IHC showing the CD34 + CD90 + ECs in HCC tumor tissue.

    Article Snippet: Subsequently, FITC-conjugated CD90 antibody was added to the sorted CD34 + endothelial cells, and an EasySepTM Release Human FITC Positive Selection Kit (STEMCELL Technologies) was used to isolate CD34 + CD90 + endothelial cells.

    Techniques: Expressing, Marker