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goat polyclonal anti rat cd31 primary antibodies  (Novus Biologicals)


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    Novus Biologicals goat polyclonal anti rat cd31 primary antibodies
    Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker <t>CD31</t> protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.
    Goat Polyclonal Anti Rat Cd31 Primary Antibodies, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/goat+polyclonal+anti+rat+cd31+primary+antibodies/pm36854041-137-28-34?v=Novus+Biologicals
    Average 91 stars, based on 1 article reviews
    goat polyclonal anti rat cd31 primary antibodies - by Bioz Stars, 2026-08
    91/100 stars

    Images

    1) Product Images from "Bioorthogonal "Click Chemistry" Bone Cement with Bioinspired Natural Mimicking Microstructures for Bone Repair."

    Article Title: Bioorthogonal "Click Chemistry" Bone Cement with Bioinspired Natural Mimicking Microstructures for Bone Repair.

    Journal: ACS biomaterials science & engineering

    doi: 10.1021/acsbiomaterials.2c01482

    Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker CD31 protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.
    Figure Legend Snippet: Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker CD31 protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.

    Techniques Used: Expressing, Immunofluorescence, Staining, Marker, Imaging

    Figure 8. In vivo osteogenesis and neovascularization. (a) In vivo osteogenic marker expression and (b) in vivo ALP activities in rat calvarial defect sites. Immunofluorescence intensity quantification of (c) ALP osteogenic maker and (d) CD31 vascular marker in tissue slices from the rat cranial defects with the PO-click-ON cement and the empty control. Immunohistochemistry (IHC)-stained images of ALP (green)/nuclei (blue) and CD31 (red)/nuclei (blue) in tissue slices from (e, f) the empty rat cranial defects and (g, h) the defects with the PO-click-ON cement. (i) Schematic demonstration of limited bone repair in the empty bone defect and the robust enhancement of bone repair by the PO-click-ON cement taking advantage of favorable cell recruitment, osteoinductivity, osteoconductivity, and neovascularization. Asterisk (*): statistically different (p < 0.05).
    Figure Legend Snippet: Figure 8. In vivo osteogenesis and neovascularization. (a) In vivo osteogenic marker expression and (b) in vivo ALP activities in rat calvarial defect sites. Immunofluorescence intensity quantification of (c) ALP osteogenic maker and (d) CD31 vascular marker in tissue slices from the rat cranial defects with the PO-click-ON cement and the empty control. Immunohistochemistry (IHC)-stained images of ALP (green)/nuclei (blue) and CD31 (red)/nuclei (blue) in tissue slices from (e, f) the empty rat cranial defects and (g, h) the defects with the PO-click-ON cement. (i) Schematic demonstration of limited bone repair in the empty bone defect and the robust enhancement of bone repair by the PO-click-ON cement taking advantage of favorable cell recruitment, osteoinductivity, osteoconductivity, and neovascularization. Asterisk (*): statistically different (p < 0.05).

    Techniques Used: In Vivo, Marker, Expressing, Immunofluorescence, Control, Immunohistochemistry, Staining



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    goat polyclonal anti rat cd31 primary antibodies  (Novus Biologicals)
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    Novus Biologicals goat polyclonal anti rat cd31 primary antibodies
    Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker <t>CD31</t> protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.
    Goat Polyclonal Anti Rat Cd31 Primary Antibodies, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/goat+polyclonal+anti+rat+cd31+primary+antibodies/pm36854041-137-28-34?v=Novus+Biologicals
    Average 91 stars, based on 1 article reviews
    goat polyclonal anti rat cd31 primary antibodies - by Bioz Stars, 2026-08
    91/100 stars
    		  Buy from Supplier

    Image Search Results


    Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker CD31 protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.

    Journal: ACS biomaterials science & engineering

    Article Title: Bioorthogonal "Click Chemistry" Bone Cement with Bioinspired Natural Mimicking Microstructures for Bone Repair.

    doi: 10.1021/acsbiomaterials.2c01482

    Figure Lengend Snippet: Figure 6. Angiogenesis. (a) Proliferation of HUVECs on the porous click-ON cements. (b) HUVEC morphology and distribution in the porous click cements with varied pore sizes. (c) mRNA expression levels of vascular markers in HUVECs growing on the cements. (d) Immunofluorescence staining of the vascular marker CD31 protein in HUVECs growing on the cements. (e) Schematic demonstration of potential support for vascular differentiation of stem cells on the porous click-ON cement and the mRNA expression level of vascular markers of (f) CD31, (g) α-SMA, (h) VEGFA, and (i) VEGFR2 in MSCs growing on the cements. (j) Immunofluorescence imaging of vascular marker CD31 protein expression in MSCs on the three types of click cements.

    Article Snippet: To determine the local neovascularization in the rat cranial defect site, immunofluorescence co-staining was performed by incubating tissue sections with rabbit monoclonal anti-ALP primary antibodies (Novus Biologicals) and goat polyclonal anti-rat CD31 primary antibodies (Novus Biologicals).

    Techniques: Expressing, Immunofluorescence, Staining, Marker, Imaging

    Figure 8. In vivo osteogenesis and neovascularization. (a) In vivo osteogenic marker expression and (b) in vivo ALP activities in rat calvarial defect sites. Immunofluorescence intensity quantification of (c) ALP osteogenic maker and (d) CD31 vascular marker in tissue slices from the rat cranial defects with the PO-click-ON cement and the empty control. Immunohistochemistry (IHC)-stained images of ALP (green)/nuclei (blue) and CD31 (red)/nuclei (blue) in tissue slices from (e, f) the empty rat cranial defects and (g, h) the defects with the PO-click-ON cement. (i) Schematic demonstration of limited bone repair in the empty bone defect and the robust enhancement of bone repair by the PO-click-ON cement taking advantage of favorable cell recruitment, osteoinductivity, osteoconductivity, and neovascularization. Asterisk (*): statistically different (p < 0.05).

    Journal: ACS biomaterials science & engineering

    Article Title: Bioorthogonal "Click Chemistry" Bone Cement with Bioinspired Natural Mimicking Microstructures for Bone Repair.

    doi: 10.1021/acsbiomaterials.2c01482

    Figure Lengend Snippet: Figure 8. In vivo osteogenesis and neovascularization. (a) In vivo osteogenic marker expression and (b) in vivo ALP activities in rat calvarial defect sites. Immunofluorescence intensity quantification of (c) ALP osteogenic maker and (d) CD31 vascular marker in tissue slices from the rat cranial defects with the PO-click-ON cement and the empty control. Immunohistochemistry (IHC)-stained images of ALP (green)/nuclei (blue) and CD31 (red)/nuclei (blue) in tissue slices from (e, f) the empty rat cranial defects and (g, h) the defects with the PO-click-ON cement. (i) Schematic demonstration of limited bone repair in the empty bone defect and the robust enhancement of bone repair by the PO-click-ON cement taking advantage of favorable cell recruitment, osteoinductivity, osteoconductivity, and neovascularization. Asterisk (*): statistically different (p < 0.05).

    Article Snippet: To determine the local neovascularization in the rat cranial defect site, immunofluorescence co-staining was performed by incubating tissue sections with rabbit monoclonal anti-ALP primary antibodies (Novus Biologicals) and goat polyclonal anti-rat CD31 primary antibodies (Novus Biologicals).

    Techniques: In Vivo, Marker, Expressing, Immunofluorescence, Control, Immunohistochemistry, Staining