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cd90  (Elabscience Biotechnology)


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    Elabscience Biotechnology cd90
    Cd90, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pe+anti+rat+cd90/PE+Anti-Rat+CD90%2FMouse+CD90%2E1+Antibody/pm41483826-71-23-26
    Average 94 stars, based on 11 article reviews
    cd90 - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: The bidirectional effects of APPswe on the osteogenic differentiation of MSCs in bone homeostasis by regulating Notch signaling
    Article Snippet: FITC anti-rat CD45, PE anti-rat CD90, and PE 160 anti-rat CD29 antibodies were obtained from Elabscience Biotechnology (Wuhan, 161 China).

    Article Title: The bidirectional effects of APPswe on the osteogenic differentiation of MSCs in bone homeostasis by regulating Notch signaling
    Article Snippet: FITC anti-rat CD45, PE anti-rat CD90, and PE anti-rat CD29 antibodies were obtained from Elabscience Biotechnology (Wuhan, China).



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    Image Search Results


    Characterization of canine adipose-derived mesenchymal stem cells (cAD-MSCs) used in this study. A Morphology of cAD-MSCs were observed under a phase-contrast microscope at 40X and 100X magnifications. B Flow cytometer was used for characterization the presence of MSC markers (CD29, CD44, and CD90), and the leukocyte common antigen (CD45) on the cell surface. C Expression of the stemness-related genes ( Oct4 and Rex1 ) and the proliferation gene ( Ki-67 ) were revealed by RT-qPCR with Gapdh normalization. D Population doubling time of cAD-MSCs in different serial passage numbers was estimated by counting cAD-MSCs after trypsinization. The linear regression curve was visualized along with a grey region of 95% confidence interval. The equation indicates the senescence rate as a slope with an annotation of the adjusted coefficient of determination ( R adj 2 ). E Adipogenic differentiation potential at day 28 post-induction was affirmed by Oil Red O staining and adipogenic related-mRNA expression ( Lep and Lpl ). F Osteogenic differentiation potential after 14-day induction was revealed by Alizarin Red S staining and the expression of osteogenic mRNA markers ( Ocn and Runx2 ). G Chondrogenic differentiation potential at day 21 post-induction was assessed by Alcian Blue staining and chondrogenic mRNA markers ( Col2a1 and Sox9 ). The mRNA expressions for multi-lineage differentiation were normalized with the reference gene ( Gapdh ) and the undifferentiation control. The scale bars represent 200 μm. In boxplots, mean values of each group were annotated at the bottom, and global statistics were stated at the top. The bars indicate pairwise comparisons (ns; no significance or p -value > 0.05, *; p -value ≤ 0.05). Abbreviation: AU; arbitrary unit

    Journal: BMC Veterinary Research

    Article Title: Small extracellular vesicles derived from sequential stimulation of canine adipose-derived mesenchymal stem cells enhance anti-inflammatory activity

    doi: 10.1186/s12917-024-04465-2

    Figure Lengend Snippet: Characterization of canine adipose-derived mesenchymal stem cells (cAD-MSCs) used in this study. A Morphology of cAD-MSCs were observed under a phase-contrast microscope at 40X and 100X magnifications. B Flow cytometer was used for characterization the presence of MSC markers (CD29, CD44, and CD90), and the leukocyte common antigen (CD45) on the cell surface. C Expression of the stemness-related genes ( Oct4 and Rex1 ) and the proliferation gene ( Ki-67 ) were revealed by RT-qPCR with Gapdh normalization. D Population doubling time of cAD-MSCs in different serial passage numbers was estimated by counting cAD-MSCs after trypsinization. The linear regression curve was visualized along with a grey region of 95% confidence interval. The equation indicates the senescence rate as a slope with an annotation of the adjusted coefficient of determination ( R adj 2 ). E Adipogenic differentiation potential at day 28 post-induction was affirmed by Oil Red O staining and adipogenic related-mRNA expression ( Lep and Lpl ). F Osteogenic differentiation potential after 14-day induction was revealed by Alizarin Red S staining and the expression of osteogenic mRNA markers ( Ocn and Runx2 ). G Chondrogenic differentiation potential at day 21 post-induction was assessed by Alcian Blue staining and chondrogenic mRNA markers ( Col2a1 and Sox9 ). The mRNA expressions for multi-lineage differentiation were normalized with the reference gene ( Gapdh ) and the undifferentiation control. The scale bars represent 200 μm. In boxplots, mean values of each group were annotated at the bottom, and global statistics were stated at the top. The bars indicate pairwise comparisons (ns; no significance or p -value > 0.05, *; p -value ≤ 0.05). Abbreviation: AU; arbitrary unit

    Article Snippet: In particular, the cells were stained with PE-conjugated mouse anti-human CD29 monoclonal antibody (BioLegend, USA), Alexa Fluor 488-conjugated rat anti-dog CD44 antibody (BioRad, USA), PE-conjugated rat anti-dog CD90 monoclonal antibody (eBioscience, USA), and FITC-conjugated mouse anti-human CD45 antibody (BioLegend, USA).

    Techniques: Derivative Assay, Microscopy, Flow Cytometry, Expressing, Quantitative RT-PCR, Staining, Control