Review



goat anti mouse cd31  (R&D Systems)


Bioz Verified Symbol R&D Systems is a verified supplier
Bioz Manufacturer Symbol R&D Systems manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 96

    Structured Review

    R&D Systems goat anti mouse cd31
    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate <t>CD31+</t> LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).
    Goat Anti Mouse Cd31, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1010 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti mouse cd31/product/R&D Systems
    Average 96 stars, based on 1010 article reviews
    goat anti mouse cd31 - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "A perfusion-independent high-throughput method to isolate liver sinusoidal endothelial cells"

    Article Title: A perfusion-independent high-throughput method to isolate liver sinusoidal endothelial cells

    Journal: Communications Biology

    doi: 10.1038/s42003-025-07458-5

    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate CD31+ LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).
    Figure Legend Snippet: a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate CD31+ LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).

    Techniques Used: Staining, Isolation, Real-time Polymerase Chain Reaction, Expressing, MANN-WHITNEY

    a – d LSECs were isolated using perfusion independent digestion method, followed by positive selection using CD146-magnetic beads. After that, enriched LSECs were placed in culture. a Primary LSEC cultures were stained for an endothelial cell marker (ERG, in green) and nuclear marker (DAPI, in gray). On the left, images show IF-stained LSEC cultures. Scale bar = 25 µm. The yellow arrow highlights an ERG-negative cell. On the right, the dot plot shows the percentage of ERG-positive cells of DAPI-positive cells. [mean ± SD, n = 3 wells]. b Images show IF-stained LSECs with CD31 (in gray), Stabilin-2 (in green), and DAPI (in blue). Scale bar = 25 µm. c Images show IF-stained LSECs with CD32b (in gray) and ERG (in green). Scale bar = 25 µm. d Representative scanning electron microscopy images of cultured LSECs. Scale bar = 2 µm.
    Figure Legend Snippet: a – d LSECs were isolated using perfusion independent digestion method, followed by positive selection using CD146-magnetic beads. After that, enriched LSECs were placed in culture. a Primary LSEC cultures were stained for an endothelial cell marker (ERG, in green) and nuclear marker (DAPI, in gray). On the left, images show IF-stained LSEC cultures. Scale bar = 25 µm. The yellow arrow highlights an ERG-negative cell. On the right, the dot plot shows the percentage of ERG-positive cells of DAPI-positive cells. [mean ± SD, n = 3 wells]. b Images show IF-stained LSECs with CD31 (in gray), Stabilin-2 (in green), and DAPI (in blue). Scale bar = 25 µm. c Images show IF-stained LSECs with CD32b (in gray) and ERG (in green). Scale bar = 25 µm. d Representative scanning electron microscopy images of cultured LSECs. Scale bar = 2 µm.

    Techniques Used: Isolation, Selection, Magnetic Beads, Staining, Marker, Electron Microscopy, Cell Culture


    Figure Legend Snippet:

    Techniques Used:



    Similar Products

    96
    Bio-Techne corporation human/mouse/rat cd31/pecam-1 antibody
    Human/Mouse/Rat Cd31/Pecam 1 Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human/mouse/rat cd31/pecam-1 antibody/product/Bio-Techne corporation
    Average 96 stars, based on 1 article reviews
    human/mouse/rat cd31/pecam-1 antibody - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    96
    R&D Systems goat anti mouse cd31
    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate <t>CD31+</t> LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).
    Goat Anti Mouse Cd31, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti mouse cd31/product/R&D Systems
    Average 96 stars, based on 1 article reviews
    goat anti mouse cd31 - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    90
    Servicebio Inc anti-cd31 goat pab #cat gb13063-50
    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate <t>CD31+</t> LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).
    Anti Cd31 Goat Pab #Cat Gb13063 50, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti-cd31 goat pab #cat gb13063-50/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    anti-cd31 goat pab #cat gb13063-50 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Novus Biologicals goat-anti-cd31 polyclonal antibody
    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate <t>CD31+</t> LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).
    Goat Anti Cd31 Polyclonal Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat-anti-cd31 polyclonal antibody/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
    goat-anti-cd31 polyclonal antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    R&D Systems Hematology goat polyclonal anti-mouse anti-rat cd31
    Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for <t>CD31.</t> ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.
    Goat Polyclonal Anti Mouse Anti Rat Cd31, supplied by R&D Systems Hematology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat polyclonal anti-mouse anti-rat cd31/product/R&D Systems Hematology
    Average 90 stars, based on 1 article reviews
    goat polyclonal anti-mouse anti-rat cd31 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Servicebio Inc anti-cd31 goat pab
    Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for <t>CD31.</t> ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.
    Anti Cd31 Goat Pab, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti-cd31 goat pab/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    anti-cd31 goat pab - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    R&D Systems Hematology goat anti‐cd31
    Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for <t>CD31.</t> ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.
    Goat Anti‐Cd31, supplied by R&D Systems Hematology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/goat anti‐cd31/product/R&D Systems Hematology
    Average 90 stars, based on 1 article reviews
    goat anti‐cd31 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Servicebio Inc anti-cd31 goat pab,
    Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for <t>CD31.</t> ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.
    Anti Cd31 Goat Pab,, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti-cd31 goat pab,/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    anti-cd31 goat pab, - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    Image Search Results


    a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate CD31+ LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).

    Journal: Communications Biology

    Article Title: A perfusion-independent high-throughput method to isolate liver sinusoidal endothelial cells

    doi: 10.1038/s42003-025-07458-5

    Figure Lengend Snippet: a – c Mice were fed with a standard or CDAA diet for 10 weeks. a Images show Picrosirius Red staining on the liver sections. LSECs were isolated from healthy and fibrotic liver tissues. Scale bar = 100 µm. b The dot plot shows the number of LSECs isolated from fibrotic mouse liver. [mean ± SD, n = 4 mice]. c Quantitative PCR analyses to compare the expression level of various sinusoidal genes in LSECs isolated from either healthy or fibrotic mouse liver tissues. [mean ± SD, n = 4 mice]. * P < 0.05 (Mann–Whitney test). d – f Liver tissues collected from healthy pigs were processed to isolate LSECs. d FACS plot showing gating strategy to isolate CD31+ LSECs and CD31− cells. e The dot plot shows the number of LSECs isolated from pig liver tissues. [mean ± SD, n = 4 pigs]. f Quantitative PCR analyses to compare expression of various vascular genes between CD31+ LSECs and CD31− cells. [mean ± SD, n = 4 pigs]. * P < 0.05 (Mann–Whitney test).

    Article Snippet: Cells were subsequently washed with PBS, fixed in 4% PFA [Carl Roth, Cat #0335.1], blocked with 10% normal donkey serum [Biozol, Cat #LIN-END9010-10] and incubated in a primary antibody mix consisting of different combinations of goat anti-mouse CD31 [R&D Systems, Cat #AF3628], goat anti-mouse CD32b [R&D Systems, Cat #AF1460], rabbit anti-mouse Desmin [Abcam, Cat # ab15200], rabbit anti-mouse ERG [Abcam, Cat #ab196149], rat anti-mouse F4/80 [BioLeegend, # 123102], and rabbit anti-mouse Stabilin-2 antibodies overnight.

    Techniques: Staining, Isolation, Real-time Polymerase Chain Reaction, Expressing, MANN-WHITNEY

    a – d LSECs were isolated using perfusion independent digestion method, followed by positive selection using CD146-magnetic beads. After that, enriched LSECs were placed in culture. a Primary LSEC cultures were stained for an endothelial cell marker (ERG, in green) and nuclear marker (DAPI, in gray). On the left, images show IF-stained LSEC cultures. Scale bar = 25 µm. The yellow arrow highlights an ERG-negative cell. On the right, the dot plot shows the percentage of ERG-positive cells of DAPI-positive cells. [mean ± SD, n = 3 wells]. b Images show IF-stained LSECs with CD31 (in gray), Stabilin-2 (in green), and DAPI (in blue). Scale bar = 25 µm. c Images show IF-stained LSECs with CD32b (in gray) and ERG (in green). Scale bar = 25 µm. d Representative scanning electron microscopy images of cultured LSECs. Scale bar = 2 µm.

    Journal: Communications Biology

    Article Title: A perfusion-independent high-throughput method to isolate liver sinusoidal endothelial cells

    doi: 10.1038/s42003-025-07458-5

    Figure Lengend Snippet: a – d LSECs were isolated using perfusion independent digestion method, followed by positive selection using CD146-magnetic beads. After that, enriched LSECs were placed in culture. a Primary LSEC cultures were stained for an endothelial cell marker (ERG, in green) and nuclear marker (DAPI, in gray). On the left, images show IF-stained LSEC cultures. Scale bar = 25 µm. The yellow arrow highlights an ERG-negative cell. On the right, the dot plot shows the percentage of ERG-positive cells of DAPI-positive cells. [mean ± SD, n = 3 wells]. b Images show IF-stained LSECs with CD31 (in gray), Stabilin-2 (in green), and DAPI (in blue). Scale bar = 25 µm. c Images show IF-stained LSECs with CD32b (in gray) and ERG (in green). Scale bar = 25 µm. d Representative scanning electron microscopy images of cultured LSECs. Scale bar = 2 µm.

    Article Snippet: Cells were subsequently washed with PBS, fixed in 4% PFA [Carl Roth, Cat #0335.1], blocked with 10% normal donkey serum [Biozol, Cat #LIN-END9010-10] and incubated in a primary antibody mix consisting of different combinations of goat anti-mouse CD31 [R&D Systems, Cat #AF3628], goat anti-mouse CD32b [R&D Systems, Cat #AF1460], rabbit anti-mouse Desmin [Abcam, Cat # ab15200], rabbit anti-mouse ERG [Abcam, Cat #ab196149], rat anti-mouse F4/80 [BioLeegend, # 123102], and rabbit anti-mouse Stabilin-2 antibodies overnight.

    Techniques: Isolation, Selection, Magnetic Beads, Staining, Marker, Electron Microscopy, Cell Culture

    Journal: Communications Biology

    Article Title: A perfusion-independent high-throughput method to isolate liver sinusoidal endothelial cells

    doi: 10.1038/s42003-025-07458-5

    Figure Lengend Snippet:

    Article Snippet: Cells were subsequently washed with PBS, fixed in 4% PFA [Carl Roth, Cat #0335.1], blocked with 10% normal donkey serum [Biozol, Cat #LIN-END9010-10] and incubated in a primary antibody mix consisting of different combinations of goat anti-mouse CD31 [R&D Systems, Cat #AF3628], goat anti-mouse CD32b [R&D Systems, Cat #AF1460], rabbit anti-mouse Desmin [Abcam, Cat # ab15200], rabbit anti-mouse ERG [Abcam, Cat #ab196149], rat anti-mouse F4/80 [BioLeegend, # 123102], and rabbit anti-mouse Stabilin-2 antibodies overnight.

    Techniques:

    Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for CD31. ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.

    Journal: Scientific Reports

    Article Title: Peripheral nerve regeneration using a bioresorbable silk fibroin-based artificial nerve conduit fabricated via a novel freeze–thaw process

    doi: 10.1038/s41598-025-88221-y

    Figure Lengend Snippet: Promotion of vascularization and macrophage-related immune response after transplantation. The SFC group showed a higher degree of vascularization and M2 macrophage recruitment than the other groups. ( A ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around the regenerated nerves, immunostained for CD31. ( B ) The total CD31-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted vascularization inside the conduit. ( C ) Representative images of the NC, SFC, Auto, and Sham groups observed using light microscopy, showing the area around and inside the regenerated nerves, immunostained for Iba1 and arginase-1. (D) The total Iba-1 and arginase-1 double-positive area of the SFC group was greater than that of the other groups, indicating that the SFC promoted M2 macrophage recruitment.

    Article Snippet: After blocking with the blocking solution; Blocking One (Nacalai Tesque, Kyoto, Japan), 20 times diluted with 0.1 M PBS containing 0.2% TritonX-100, the following primary antibodies were applied: rabbit polyclonal anti-neurofilament heavy (NFH) polypeptide antibody (ab8135; 1:500 dilution; Abcam), chicken myelin basic protein polyclonal anti-peptide antibody (MBP88837983; 1:500 dilution; Aves), goat polyclonal anti-mouse and anti-rat CD31 (AF3628; 1:100 dilution; R&D), rabbit polyclonal anti-Iba1 antibody (GtX100042; 1:500 dilution; GeneTex), and goat polyclonal anti-arginase-1 antibody (ab60176; 1:100 dilution; Abcam).

    Techniques: Transplantation Assay, Light Microscopy