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cd29 antibodies conjugated with pe  (Miltenyi Biotec)


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    Miltenyi Biotec cd29 antibodies conjugated with pe
    Identification and culturing of human artSPCs and chondrocytes. ( A ) Identification of <t>CD29</t> as a marker for human superficial cells by immunostaining. ( B-E ) Colony formation by CD29 low and CD29 high cells. ( F-I ) Toluidine blue staining and immunostaining for ( F ʹ -I ʹ ) Sox9, ( F ″- I ″) collagen type I, ( F ″ ʹ -I ″ ʹ ) collagen type I, and ( F″″-I″″ ) Mef2c in pellets from CD29 low and CD29 high cells expanded in the presence of DAPT or vehicle (DMSO). Cell nuclei were stained blue with DAPI. Quantification of ( J ) Sox9, ( K ) collagen type II, ( L ) collagen type I, and ( M ) Mef2c in these same pellets. ( N ) Cumulative cell number (CCN) relative to the corresponding controls. Representative images of 5 independent experiments. * P < .05, **** P < .0001, as determined by the unpaired t -test. n = 5 patients in all cases.
    Cd29 Antibodies Conjugated With Pe, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 71 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cd29 antibodies conjugated with pe/product/Miltenyi Biotec
    Average 94 stars, based on 71 article reviews
    cd29 antibodies conjugated with pe - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Notch Signaling Regulates the Chondrogenic Potential of Both Articular Chondrocytes and Their Progenitors During Expansion"

    Article Title: Notch Signaling Regulates the Chondrogenic Potential of Both Articular Chondrocytes and Their Progenitors During Expansion

    Journal: Stem Cells

    doi: 10.1093/stmcls/sxad031

    Identification and culturing of human artSPCs and chondrocytes. ( A ) Identification of CD29 as a marker for human superficial cells by immunostaining. ( B-E ) Colony formation by CD29 low and CD29 high cells. ( F-I ) Toluidine blue staining and immunostaining for ( F ʹ -I ʹ ) Sox9, ( F ″- I ″) collagen type I, ( F ″ ʹ -I ″ ʹ ) collagen type I, and ( F″″-I″″ ) Mef2c in pellets from CD29 low and CD29 high cells expanded in the presence of DAPT or vehicle (DMSO). Cell nuclei were stained blue with DAPI. Quantification of ( J ) Sox9, ( K ) collagen type II, ( L ) collagen type I, and ( M ) Mef2c in these same pellets. ( N ) Cumulative cell number (CCN) relative to the corresponding controls. Representative images of 5 independent experiments. * P < .05, **** P < .0001, as determined by the unpaired t -test. n = 5 patients in all cases.
    Figure Legend Snippet: Identification and culturing of human artSPCs and chondrocytes. ( A ) Identification of CD29 as a marker for human superficial cells by immunostaining. ( B-E ) Colony formation by CD29 low and CD29 high cells. ( F-I ) Toluidine blue staining and immunostaining for ( F ʹ -I ʹ ) Sox9, ( F ″- I ″) collagen type I, ( F ″ ʹ -I ″ ʹ ) collagen type I, and ( F″″-I″″ ) Mef2c in pellets from CD29 low and CD29 high cells expanded in the presence of DAPT or vehicle (DMSO). Cell nuclei were stained blue with DAPI. Quantification of ( J ) Sox9, ( K ) collagen type II, ( L ) collagen type I, and ( M ) Mef2c in these same pellets. ( N ) Cumulative cell number (CCN) relative to the corresponding controls. Representative images of 5 independent experiments. * P < .05, **** P < .0001, as determined by the unpaired t -test. n = 5 patients in all cases.

    Techniques Used: Marker, Immunostaining, Staining



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    Image Search Results


    Identification and culturing of human artSPCs and chondrocytes. ( A ) Identification of CD29 as a marker for human superficial cells by immunostaining. ( B-E ) Colony formation by CD29 low and CD29 high cells. ( F-I ) Toluidine blue staining and immunostaining for ( F ʹ -I ʹ ) Sox9, ( F ″- I ″) collagen type I, ( F ″ ʹ -I ″ ʹ ) collagen type I, and ( F″″-I″″ ) Mef2c in pellets from CD29 low and CD29 high cells expanded in the presence of DAPT or vehicle (DMSO). Cell nuclei were stained blue with DAPI. Quantification of ( J ) Sox9, ( K ) collagen type II, ( L ) collagen type I, and ( M ) Mef2c in these same pellets. ( N ) Cumulative cell number (CCN) relative to the corresponding controls. Representative images of 5 independent experiments. * P < .05, **** P < .0001, as determined by the unpaired t -test. n = 5 patients in all cases.

    Journal: Stem Cells

    Article Title: Notch Signaling Regulates the Chondrogenic Potential of Both Articular Chondrocytes and Their Progenitors During Expansion

    doi: 10.1093/stmcls/sxad031

    Figure Lengend Snippet: Identification and culturing of human artSPCs and chondrocytes. ( A ) Identification of CD29 as a marker for human superficial cells by immunostaining. ( B-E ) Colony formation by CD29 low and CD29 high cells. ( F-I ) Toluidine blue staining and immunostaining for ( F ʹ -I ʹ ) Sox9, ( F ″- I ″) collagen type I, ( F ″ ʹ -I ″ ʹ ) collagen type I, and ( F″″-I″″ ) Mef2c in pellets from CD29 low and CD29 high cells expanded in the presence of DAPT or vehicle (DMSO). Cell nuclei were stained blue with DAPI. Quantification of ( J ) Sox9, ( K ) collagen type II, ( L ) collagen type I, and ( M ) Mef2c in these same pellets. ( N ) Cumulative cell number (CCN) relative to the corresponding controls. Representative images of 5 independent experiments. * P < .05, **** P < .0001, as determined by the unpaired t -test. n = 5 patients in all cases.

    Article Snippet: Five hundred thousand human cells were stained with CD29 antibodies conjugated with PE (Miltenyi Biotec, clone TS2/16, 1:100, 100 uL per aliquot).

    Techniques: Marker, Immunostaining, Staining

    Characterization of MSC-EXs. (a) NTA analysis of MSC-EX size. (b) CD29 and CD63 expressions were determined by flow cytometry. Red line: isotype control; blue line: CD29 positive. (c) Representative image of MSC-EXs examined by TEM.

    Journal: Stem Cells International

    Article Title: Exosomes Derived from Mesenchymal Stem Cells Ameliorate Hypoxia/Reoxygenation-Injured ECs via Transferring MicroRNA-126

    doi: 10.1155/2019/2831756

    Figure Lengend Snippet: Characterization of MSC-EXs. (a) NTA analysis of MSC-EX size. (b) CD29 and CD63 expressions were determined by flow cytometry. Red line: isotype control; blue line: CD29 positive. (c) Representative image of MSC-EXs examined by TEM.

    Article Snippet: To define MSC-EXs, samples were stained with 5 μ L of PE-conjugated anti-mouse CD29 antibody (BD Biosciences) and analyzed by flow cytometry.

    Techniques: Flow Cytometry