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rabbit polyclonal anti cd34  (Boster Bio)


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    Boster Bio rabbit polyclonal anti cd34
    Rabbit Polyclonal Anti Cd34, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+cd34/Anti-CD34+Antibody+Picoband/pmc11987403-92-6-11
    Average 91 stars, based on 7 article reviews
    rabbit polyclonal anti cd34 - by Bioz Stars, 2026-09
    91/100 stars

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    Article Title: Insufficient radiofrequency ablation promotes angiogenesis of residual hepatocellular carcinoma via HIF-1α/VEGFA.
    Article Snippet: Antibodies used in the present study include the following: The rabbit polyclonal anti-CD34, anti-VEGFA and anti-b-actin antibodies were purchased from Boster (Wuhan, China).

    Article Title: Insufficient Radiofrequency Ablation Promotes Angiogenesis of Residual Hepatocellular Carcinoma via HIF-1α/VEGFA
    Article Snippet: Antibodies used in the present study include the following: The rabbit polyclonal anti-CD34, anti-VEGFA and anti-β-actin antibodies were purchased from Boster (Wuhan, China).

    Article Title: Novel dopamine-modified oxidized sodium alginate hydrogels promote angiogenesis and accelerate healing of chronic diabetic wounds.
    Article Snippet: Herein, the dopamine (DA) was grafted with oxidized sodium alginate (OSA) via Schiff base reduction reaction, aiming to fabricate novel DA-grafted OSA (OSA-DA) hydrogels with enhanced biocompatibility and suitable adhesion for clinical applications.. The chemical structures of OSA-DA were characterized via UV–Vis, FTIR and 1H NMR spectroscopy analysis.. The hydrogel characteristics, biocompatibility, as well as the chronic diabetic wound healing efficacy were investigated.

    Incubation:

    Article Title: D-chiro-inositol effectively counteracts endometriosis in a mouse model
    Article Snippet: The sections were then subjected to a treatment to block endogenous peroxidase activity (Dako). .. The sections were then incubated with rabbit polyclonal anti-CD34 (1:200, PA1334, Boster Biological technology Pleasanton, CA, USA) (Egorova et al. ), anti-IL-1β (1:500, NBP1-42767, Novus biologicals, CO, USA, anti-E-Cadherin (1:200, BS1098, Bioworld Technology, MN, USA) (Ntzeros et al. ) antibodies in 1% BSA/PBS overnight at + 4 °C. .. For PCNA staining, after thorough washing, sections were incubated with M.O.M mouse IgG blocking reagent (Vector Laboratories Burlingame, CA, USA) overnight at 4 °C according to the manufacturer’s protocol and then incubated with mouse monoclonal anti-PCNA antibody (1:500, NB500-106, Novus Biological) (Mishra et al. ) diluted in mouse on mouse (M.O.M) diluent for 30 min, according to the Vector Laboratories instructions.

    Article Title: Therapeutic gene expression in transduced mesenchymal stem cells can be monitored using a reporter gene.
    Article Snippet: Contents lists available at SciVerse ScienceDirect Nuclear Medicine and Biology j ourna l homepage: www.e lsev ie r.com/ locate /nucmedb io Therapeutic gene expression in transduced mesenchymal stem cells can be monitored using a reporter gene Guopeng Zhang a, Xiaoli Lan a,⁎, Tzu-Chen Yen b, Quan Chen a, Zhijun Pei a, Chunxia Qin a, Yongxue Zhang a,⁎ a Department of Nuclear Medicine, Union Hospital, Tongji Medical College of Huazhong University of Science and Technology, Hubei Province Key Laboratory of Molecular Imaging, Wuhan, 430022, China b Molecular Imaging Center and Department of Nuclear Medicine, Chang Gung Memorial Hospital-Linkou, Taoyuan, 330, Taiwan ⁎ Corresponding authors at: Department of Nuclear M Medical College of Huazhong University of Science and T Laboratory of Molecular Imaging, No.1277, Jiefang Av Province, China.. Tel.. : +86 27 85726282; fax: +86 27 8 E-mail addresses: LXL730724@hotmail.com (X. Lan) (Y. Zhang).

    Article Title: D-chiro-inositol effectively counteracts endometriosis in a mouse model.
    Article Snippet: The sections were then subjected to a treatment to block endogenous peroxidase activity (Dako). .. The sections were then incubated with rabbit polyclonal anti-CD34 (1:200, PA1334, Boster Biological technology Pleasanton, CA, USA) (Egorova et al. 2023), anti-IL-1β (1:500, NBP1-42767, Novus biologicals, CO, USA, anti-E-Cadherin (1:200, BS1098, Bioworld Technology, MN, USA) (Ntzeros et al. 2025) antibodies in 1% BSA/PBS overnight at + 4 °C. .. The sections were then subjected to a treatment to block endogenous peroxidase activity (Dako).



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    Exosomal miR-144-3p involved in PPT regulation and MCD in response to neurogenic inflammation and peripheral nociceptor hypersensitivity. ( A ) Immunohistochemical staining images showing colocalization of <t>CD34</t> (MCs; red) and PGP9.5 (axons; green). Cell nuclei were stained with DAPI (blue). ( B ) Quantitative analyses of the colocalization of CD34 (MCs) and PGP9.5 (axons) (n = 3 per group). ( C ) The ratio of the number of cells expressing both CD34 (MCs) and PGP9.5 (axons) to the number of CD34 + MCs (n = 3 per group). All data are shown as the mean ± SD, ∗∗ P < 0.01, ## P < 0.01.
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    Immunofluorescence and immunohistochemical analysis in fistula tissues. (A) Representative immunofluorescence staining of <t>CD34</t> (red) and DAPI (blue) in fistula tissues from Control, PRP, and Cryo-PRP groups. (B) Quantitative analysis of CD34 expression using integrated optical density (IOD/Area). (C) Representative images of immunohistochemical staining for α-SMA, CD31, VEGF, PCNA, and TNF-α in the Control, PRP, and Cryo-PRP groups are shown (original magnification: ×400). Expression of α-SMA, CD31, VEGF, and PCNA was markedly increased in the PRP and Cryo-PRP groups compared to Control, with the highest levels observed in the Cryo-PRP group. In contrast, TNF-α expression was significantly reduced following PRP and Cryo-PRP treatment, with minimal staining in the Cryo-PRP group. (D) Quantitative analysis of immunohistochemical staining using integrated optical density per area (IOD/Area × 10 6 ). Data are presented as mean ± SD. * P < 0.05 vs. Control; *** P < 0.001 vs. Control.
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    Image Search Results


    Exosomal miR-144-3p involved in PPT regulation and MCD in response to neurogenic inflammation and peripheral nociceptor hypersensitivity. ( A ) Immunohistochemical staining images showing colocalization of CD34 (MCs; red) and PGP9.5 (axons; green). Cell nuclei were stained with DAPI (blue). ( B ) Quantitative analyses of the colocalization of CD34 (MCs) and PGP9.5 (axons) (n = 3 per group). ( C ) The ratio of the number of cells expressing both CD34 (MCs) and PGP9.5 (axons) to the number of CD34 + MCs (n = 3 per group). All data are shown as the mean ± SD, ∗∗ P < 0.01, ## P < 0.01.

    Journal: Journal of Traditional and Complementary Medicine

    Article Title: Plasma-derived exosomal miR-144-3p targeting IL-1β is involved in pressure pain threshold regulation at PC6 acupoint in myocardial ischemia rats

    doi: 10.1016/j.jtcme.2025.02.001

    Figure Lengend Snippet: Exosomal miR-144-3p involved in PPT regulation and MCD in response to neurogenic inflammation and peripheral nociceptor hypersensitivity. ( A ) Immunohistochemical staining images showing colocalization of CD34 (MCs; red) and PGP9.5 (axons; green). Cell nuclei were stained with DAPI (blue). ( B ) Quantitative analyses of the colocalization of CD34 (MCs) and PGP9.5 (axons) (n = 3 per group). ( C ) The ratio of the number of cells expressing both CD34 (MCs) and PGP9.5 (axons) to the number of CD34 + MCs (n = 3 per group). All data are shown as the mean ± SD, ∗∗ P < 0.01, ## P < 0.01.

    Article Snippet: The sections were incubated with primary antibodies including a rabbit polyclonal anti-CD34 antibody (Affinity Biosciences, Cincinnati, Ohio, USA) and rabbit polyclonal anti-Protein gene product 9.5 (PGP9.5) antibody (Affinity Biosciences, Cincinnati, Ohio, USA).

    Techniques: Immunohistochemical staining, Staining, Expressing

    Immunofluorescence and immunohistochemical analysis in fistula tissues. (A) Representative immunofluorescence staining of CD34 (red) and DAPI (blue) in fistula tissues from Control, PRP, and Cryo-PRP groups. (B) Quantitative analysis of CD34 expression using integrated optical density (IOD/Area). (C) Representative images of immunohistochemical staining for α-SMA, CD31, VEGF, PCNA, and TNF-α in the Control, PRP, and Cryo-PRP groups are shown (original magnification: ×400). Expression of α-SMA, CD31, VEGF, and PCNA was markedly increased in the PRP and Cryo-PRP groups compared to Control, with the highest levels observed in the Cryo-PRP group. In contrast, TNF-α expression was significantly reduced following PRP and Cryo-PRP treatment, with minimal staining in the Cryo-PRP group. (D) Quantitative analysis of immunohistochemical staining using integrated optical density per area (IOD/Area × 10 6 ). Data are presented as mean ± SD. * P < 0.05 vs. Control; *** P < 0.001 vs. Control.

    Journal: Frontiers in Bioengineering and Biotechnology

    Article Title: A novel cryoprecipitate-enriched PRP (Cryo-PRP) gel with enhanced mechanical strength and regenerative capacity accelerates enterocutaneous fistula healing

    doi: 10.3389/fbioe.2025.1668608

    Figure Lengend Snippet: Immunofluorescence and immunohistochemical analysis in fistula tissues. (A) Representative immunofluorescence staining of CD34 (red) and DAPI (blue) in fistula tissues from Control, PRP, and Cryo-PRP groups. (B) Quantitative analysis of CD34 expression using integrated optical density (IOD/Area). (C) Representative images of immunohistochemical staining for α-SMA, CD31, VEGF, PCNA, and TNF-α in the Control, PRP, and Cryo-PRP groups are shown (original magnification: ×400). Expression of α-SMA, CD31, VEGF, and PCNA was markedly increased in the PRP and Cryo-PRP groups compared to Control, with the highest levels observed in the Cryo-PRP group. In contrast, TNF-α expression was significantly reduced following PRP and Cryo-PRP treatment, with minimal staining in the Cryo-PRP group. (D) Quantitative analysis of immunohistochemical staining using integrated optical density per area (IOD/Area × 10 6 ). Data are presented as mean ± SD. * P < 0.05 vs. Control; *** P < 0.001 vs. Control.

    Article Snippet: Subsequently, the sections were incubated overnight at 4 °C with rabbit anti-CD34 antibody (BIOSS, bs-064R; 1:100 dilution).

    Techniques: Immunofluorescence, Immunohistochemical staining, Staining, Control, Expressing