cd68 polyclonal antibody, pe conjugated Search Results


cd68 antibody  (Bioss)
94
Bioss cd68 antibody
Inflammatory response of different SF/PLLA nanoyarn-based woven fabrics after 14 days of subcutaneous implantation. (a) Design of the subcutaneous implantation experiment. (b) H&E staining, M&T staining and <t>CD68</t> (red) immunofluorescent staining of different SF/PLLA woven fabrics after subcutaneously implanted in rat for 14 days. Blue fluorescent was utilized to visualize the nuclei for immunofluorescent staining. The pentacles stand for nanoyarns existed in the woven fabrics. Scale bars for H&E staining and M&T staining: 100 ​μm. Scale bars for immunofluorescent staining: 50 ​μm. (c) Quantitative analysis of thickness of dense collagen layer surrounding the implanted textiles (n ​= ​3; ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (d) Quantitative analysis of CD68 intensity inside the different SF/PLLA woven fabrics (n ​= ​3; ∗p ​< ​0.05, ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Cd68 Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd68 antibody/product/Bioss
Average 94 stars, based on 1 article reviews
cd68 antibody - by Bioz Stars, 2026-05
94/100 stars
  Buy from Supplier
cd68 polyclonal antibody, pe conjugated  (Bioss)
94
Bioss cd68 polyclonal antibody, pe conjugated
Inflammatory response of different SF/PLLA nanoyarn-based woven fabrics after 14 days of subcutaneous implantation. (a) Design of the subcutaneous implantation experiment. (b) H&E staining, M&T staining and <t>CD68</t> (red) immunofluorescent staining of different SF/PLLA woven fabrics after subcutaneously implanted in rat for 14 days. Blue fluorescent was utilized to visualize the nuclei for immunofluorescent staining. The pentacles stand for nanoyarns existed in the woven fabrics. Scale bars for H&E staining and M&T staining: 100 ​μm. Scale bars for immunofluorescent staining: 50 ​μm. (c) Quantitative analysis of thickness of dense collagen layer surrounding the implanted textiles (n ​= ​3; ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (d) Quantitative analysis of CD68 intensity inside the different SF/PLLA woven fabrics (n ​= ​3; ∗p ​< ​0.05, ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Cd68 Polyclonal Antibody, Pe Conjugated, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd68 polyclonal antibody, pe conjugated/product/Bioss
Average 94 stars, based on 1 article reviews
cd68 polyclonal antibody, pe conjugated - by Bioz Stars, 2026-05
94/100 stars
  Buy from Supplier
cd68 polyclonal antibody, pe-cy3 conjugated  (Bioss)
N/A
This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages. It is a member of the lysosomal/endosomal-associated membrane glycoprotein (LAMP) family. The protein primarily localizes to lysosomes and
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cd68 polyclonal antibody, pe-cy7 conjugated  (Bioss)
N/A
Could play a role in phagocytic activities of tissue macrophages, both in intracellular lysosomal metabolism and extracellular cell-cell and cell-pathogen interactions. Binds to tissue- and organ-specific lectins or selectins, allowing homing of macrophage subsets to
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cd68 polyclonal antibody, pe-cy5.5 conjugated  (Bioss)
N/A
Could play a role in phagocytic activities of tissue macrophages, both in intracellular lysosomal metabolism and extracellular cell-cell and cell-pathogen interactions. Binds to tissue- and organ-specific lectins or selectins, allowing homing of macrophage subsets to
   Buy from Supplier
cd68 polyclonal antibody, pe-cy5 conjugated  (Bioss)
N/A
This gene encodes a 110-kD transmembrane glycoprotein that is highly expressed by human monocytes and tissue macrophages. It is a member of the lysosomal/endosomal-associated membrane glycoprotein (LAMP) family. The protein primarily localizes to lysosomes and
   Buy from Supplier

Image Search Results


Inflammatory response of different SF/PLLA nanoyarn-based woven fabrics after 14 days of subcutaneous implantation. (a) Design of the subcutaneous implantation experiment. (b) H&E staining, M&T staining and CD68 (red) immunofluorescent staining of different SF/PLLA woven fabrics after subcutaneously implanted in rat for 14 days. Blue fluorescent was utilized to visualize the nuclei for immunofluorescent staining. The pentacles stand for nanoyarns existed in the woven fabrics. Scale bars for H&E staining and M&T staining: 100 ​μm. Scale bars for immunofluorescent staining: 50 ​μm. (c) Quantitative analysis of thickness of dense collagen layer surrounding the implanted textiles (n ​= ​3; ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (d) Quantitative analysis of CD68 intensity inside the different SF/PLLA woven fabrics (n ​= ​3; ∗p ​< ​0.05, ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Electrospun strong, bioactive, and bioabsorbable silk fibroin/poly (L-lactic-acid) nanoyarns for constructing advanced nanotextile tissue scaffolds

doi: 10.1016/j.mtbio.2022.100243

Figure Lengend Snippet: Inflammatory response of different SF/PLLA nanoyarn-based woven fabrics after 14 days of subcutaneous implantation. (a) Design of the subcutaneous implantation experiment. (b) H&E staining, M&T staining and CD68 (red) immunofluorescent staining of different SF/PLLA woven fabrics after subcutaneously implanted in rat for 14 days. Blue fluorescent was utilized to visualize the nuclei for immunofluorescent staining. The pentacles stand for nanoyarns existed in the woven fabrics. Scale bars for H&E staining and M&T staining: 100 ​μm. Scale bars for immunofluorescent staining: 50 ​μm. (c) Quantitative analysis of thickness of dense collagen layer surrounding the implanted textiles (n ​= ​3; ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (d) Quantitative analysis of CD68 intensity inside the different SF/PLLA woven fabrics (n ​= ​3; ∗p ​< ​0.05, ∗∗p ​< ​0.001, ∗∗∗p ​< ​0.0001). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: Moreover, some slides were double stained with CD68 antibody (Bioss, China) and DAPI (Yeasen, China), and observed with a Zeiss 900 CLSM, in order to investigate the inflammation response of four different SF/PLLA woven fabrics.

Techniques: Staining