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anti rabbit cd31 platelet endothelial cell adhesion molecule  (Novus Biologicals)


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    Structured Review

    Novus Biologicals anti rabbit cd31 platelet endothelial cell adhesion molecule
    Anti Rabbit Cd31 Platelet Endothelial Cell Adhesion Molecule, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 96/100, based on 184 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+rabbit+cd31+platelet+endothelial+cell+adhesion+molecule/CD31%2FPECAM-1+Antibody/pmc13046712-149-9-19
    Average 96 stars, based on 184 article reviews
    anti rabbit cd31 platelet endothelial cell adhesion molecule - by Bioz Stars, 2026-11
    96/100 stars

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    Incubation:

    Article Title: Cellulase-assisted platelet-rich plasma release from nanofibrillated cellulose hydrogel enhances wound healing.
    Article Snippet: Then, endogenous peroxidase activity was blocked with 3% H2O2 for 10 min. Next, sections were blocked in 5% bovine serum albumin (BSA, Merck, Germany) in Tris buffered saline with Tween 20 (TBS-T, Merck, Germany) for 1 h followed by blocking with endogenous biotin (Avidin/Biotin blocking kit, Vector Laboratories, CA, USA) for 15 min first with Avidin and then with Biotin. .. Tissue sections were incubated with anti-rabbit CD31/platelet endothelial cell adhesion molecule (CD31/PECAM-1, 1:500, CAT: NB100–2284, Novus Biologicals, UK), and anti-mouse proliferating cell nuclear antigen (PCNA, F-2, 1:500, CAT: SC-25280, Santa Cruz Biotechnology Inc., TX, USA), as a primary antibodies in 3% BSA/TBS-T overnight at 4 ◦C. .. After washing with TBS-T, tissue sections were stained with biotinylated secondary antibody, goat anti-rabbit or goat antimouse IgG (1:1000, Abcam, UK) in 3% BSA/TBS-T for 1 h. VECTASTAIN Elite ABC reagents (Vector Laboratories) were used for antibody detection by staining the tissue sections for 30 min at room temperature, after which they were treated with 3,3′-diaminobenzidine (DAB) HRP substrate treatment (Vector Laboratories).

    Article Title: Towards a standardized diabetic prolonged wound healing model in hairless SKH1 mice
    Article Snippet: Next, sections were blocked with endogenous biotin (Avidin/Biotin blocking kit, Vector Laboratories, CA, USA) for 15 min with Avidin first and then 15 min with Biotin. .. Tissue sections were incubated overnight at 4 °C with anti-rabbit CD31/platelet endothelial cell adhesion molecule (CD31/PECAM-1, 1:100, CAT: NB100–2284, Novus Biologicals, UK) or 1 h at room temperature with anti-rabbit ionized calcium-binding adaptor molecule 1 (Iba-1, 1:500, CAT: 019-19741, FujiFilm, USA) or anti-rabbit lysozyme (LZM, 1:1000, CAT: A0099, Agilent, CA, USA) as a primary antibody in 3% BSA/TBS-T. After washing with TBS-T, tissue sections were stained for 1 h at room temperature with goat anti-rabbit IgG as biotinylated secondary antibody (1:1000 for CD31 and 1:200 for Iba1 and LZM, Abcam, UK) in 3% BSA/TBS-T. VECTASTAIN Elite ABC reagents (Vector Laboratories) were used for antibody detection by staining the tissue sections for 30 min at room temperature, after which they were treated with 3,3′-diaminobenzidine (DAB) HRP substrate treatment (Vector Laboratories). .. All stained tissue sections were counterstained with hematoxylin, dehydrated, and covered with cover clips using a mounting medium (Coverquick 2000, VWR International, PA, USA).

    Staining:

    Article Title: Towards a standardized diabetic prolonged wound healing model in hairless SKH1 mice
    Article Snippet: Next, sections were blocked with endogenous biotin (Avidin/Biotin blocking kit, Vector Laboratories, CA, USA) for 15 min with Avidin first and then 15 min with Biotin. .. Tissue sections were incubated overnight at 4 °C with anti-rabbit CD31/platelet endothelial cell adhesion molecule (CD31/PECAM-1, 1:100, CAT: NB100–2284, Novus Biologicals, UK) or 1 h at room temperature with anti-rabbit ionized calcium-binding adaptor molecule 1 (Iba-1, 1:500, CAT: 019-19741, FujiFilm, USA) or anti-rabbit lysozyme (LZM, 1:1000, CAT: A0099, Agilent, CA, USA) as a primary antibody in 3% BSA/TBS-T. After washing with TBS-T, tissue sections were stained for 1 h at room temperature with goat anti-rabbit IgG as biotinylated secondary antibody (1:1000 for CD31 and 1:200 for Iba1 and LZM, Abcam, UK) in 3% BSA/TBS-T. VECTASTAIN Elite ABC reagents (Vector Laboratories) were used for antibody detection by staining the tissue sections for 30 min at room temperature, after which they were treated with 3,3′-diaminobenzidine (DAB) HRP substrate treatment (Vector Laboratories). .. All stained tissue sections were counterstained with hematoxylin, dehydrated, and covered with cover clips using a mounting medium (Coverquick 2000, VWR International, PA, USA).



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    Figure 4. Effects of konjac flour (KF) and combined dietary fiber (CDF) supplementation during the last 50 days of gestation on placental angiogenesis of gilts. (A) The hematoxylin and eosin methods were used to examine blood vessel density in the CON, KF, and CDF placental tissues, with black arrows for placental blood vessels (bar = 50 μm). (B) The percentage of blood vessels in the placental tissues. Each gilt was regarded as an experimental unit (n = 6 per group). (C) Western blot analysis of angiogenesis-related factors and protein expression in different placentae. (D) Protein expression levels of <t>CD31</t> and VEGF-A. Each placenta was regarded as an experimental unit (n = 12 per group). a,bMean values with different small letters indicate a significant difference at P < 0.05.
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    Figure 4. Effects of konjac flour (KF) and combined dietary fiber (CDF) supplementation during the last 50 days of gestation on placental angiogenesis of gilts. (A) The hematoxylin and eosin methods were used to examine blood vessel density in the CON, KF, and CDF placental tissues, with black arrows for placental blood vessels (bar = 50 μm). (B) The percentage of blood vessels in the placental tissues. Each gilt was regarded as an experimental unit (n = 6 per group). (C) Western blot analysis of angiogenesis-related factors and protein expression in different placentae. (D) Protein expression levels of <t>CD31</t> and VEGF-A. Each placenta was regarded as an experimental unit (n = 12 per group). a,bMean values with different small letters indicate a significant difference at P < 0.05.
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    Figure 4. Effects of konjac flour (KF) and combined dietary fiber (CDF) supplementation during the last 50 days of gestation on placental angiogenesis of gilts. (A) The hematoxylin and eosin methods were used to examine blood vessel density in the CON, KF, and CDF placental tissues, with black arrows for placental blood vessels (bar = 50 μm). (B) The percentage of blood vessels in the placental tissues. Each gilt was regarded as an experimental unit (n = 6 per group). (C) Western blot analysis of angiogenesis-related factors and protein expression in different placentae. (D) Protein expression levels of CD31 and VEGF-A. Each placenta was regarded as an experimental unit (n = 12 per group). a,bMean values with different small letters indicate a significant difference at P < 0.05.

    Journal: Journal of animal science

    Article Title: Dietary fiber supplementation during the last 50 days of gestation improves the farrowing performance of gilts by modulating insulin sensitivity, gut microbiota, and placental function.

    doi: 10.1093/jas/skad021

    Figure Lengend Snippet: Figure 4. Effects of konjac flour (KF) and combined dietary fiber (CDF) supplementation during the last 50 days of gestation on placental angiogenesis of gilts. (A) The hematoxylin and eosin methods were used to examine blood vessel density in the CON, KF, and CDF placental tissues, with black arrows for placental blood vessels (bar = 50 μm). (B) The percentage of blood vessels in the placental tissues. Each gilt was regarded as an experimental unit (n = 6 per group). (C) Western blot analysis of angiogenesis-related factors and protein expression in different placentae. (D) Protein expression levels of CD31 and VEGF-A. Each placenta was regarded as an experimental unit (n = 12 per group). a,bMean values with different small letters indicate a significant difference at P < 0.05.

    Article Snippet: After blocking with TBS/T buffer containing 5% milk, the membranes were incubated with the primary antibodies against vascular endothelial growth factor A (VEGF-A) (19003-1-AP, Proteintech, USA, 1:1,000), platelet endothelial cell adhesion molecule (CD31) (A0378, Abclonal, China, 1:1,000), and β-actin (4970, CST, USA, 1:1,000).

    Techniques: Western Blot, Expressing