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anti β2 integrin proteintech  (Proteintech)


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    Structured Review

    Proteintech anti β2 integrin proteintech
    Anti β2 Integrin Proteintech, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 84 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+cd11b/CD11B%2FIntegrin+alpha+M+Antibody/pm42814515-211-20-21
    Average 94 stars, based on 84 article reviews
    anti β2 integrin proteintech - by Bioz Stars, 2026-10
    94/100 stars

    Images

    Related Articles

    other:

    Article Title: A polymerized probucol nanoformulation with neutrophil extracellular vesicle camouflage for cerebral ischemia-reperfusion injury therapy
    Article Snippet: The BCA protein assay kit, DiD, DiO, DAPI, hematoxylin and eosin (H&E), apoptosis detection kit, FITC phalloidin, LysoTracker Green, and DHE (dihydroethidium) assay kits were purchased from Beyotime Biotechnology (Shanghai, China).

    Bioprocessing:

    Article Title: Conjugated bile acids alleviate acute pancreatitis through inhibition of TGR5 and NLRP3 mediated inflammation
    Article Snippet: .. Antibodies used: anti-CD11b (2185–1-ap; Proteintech), and anti-F4/80 (cst70076; Cell Signaling Technology) monoclonal antibodies, and anti-Ly6G monoclonal antibody (65,140–1-ig; Proteintech). .. After incubation with the primary antibody overnight at 4 °C, the secondary antibody (Proteintech) was added and incubated at room temperature for 30 min. Stained sections were imaged with a Nikon Eclipse C1 vertical fluores-cence microscope.

    Article Title: Conjugated bile acids alleviate acute pancreatitis through inhibition of TGR5 and NLRP3 mediated inflammation.
    Article Snippet: .. Antibodies used: anti-CD11b (2185–1-ap; Proteintech), and anti-F4/80 (cst70076; Cell Signaling Technology) monoclonal antibodies, and anti-Ly6G monoclonal antibody (65,140–1-ig; Proteintech). .. After incubation with the primary antibody overnight at 4 °C, the secondary antibody (Proteintech) was added and incubated at room temperature for 30 min. Stained sections were imaged with a Nikon Eclipse C1 vertical fluores-cence microscope.

    Blocking Assay:

    Article Title: Macrophage-derived S100A9 promotes diabetic cardiomyopathy by disturbing mitochondrial quality control via STAT3 activation
    Article Snippet: .. After blocking in 1% goat serum for 1 hour at 37°C, staining was performed as above with anti-S100A9 (1:100 dilution, #73425, CST), anti-α-actinin (1:100 dilution, 66895-1-Ig, Proteintech), anti-CD11b (1:100 dilution, 66519-1-Ig, Proteintech), anti-CD80 (1:100 dilution, M1007-10, HUABIO), anti-F4/80 (1:100 dilution, P47789 , Abmart), and anti-CCR2 (1:100 dilution, TD7507M, Abmart) antibodies. .. Slides were washed and then incubated with FITC Goat Anti-Rabbit IgG (H+L) (AS011, ABclonal) and Cy3 Goat Anti-Mouse IgG (H+L) (AS008, ABclonal).

    Article Title: Macrophage-derived S100A9 promotes diabetic cardiomyopathy by disturbing mitochondrial quality control via STAT3 activation.
    Article Snippet: .. After blocking in 1% goat serum for 1 hour at 37°C, staining was performed as above with anti-S100A9 (1:100 dilution, #73425, CST), anti-α-actinin (1:100 dilution, 66895-1-Ig, Proteintech), anti-CD11b (1:100 dilution, 66519-1-Ig, Proteintech), anti-CD80 (1:100 dilution, M1007-10, HUABIO), anti-F4/80 (1:100 dilution, P47789, Abmart), and anti-CCR2 (1:100 dilution, TD7507M, Abmart) antibodies. .. Slides were washed and then incubated with FITC Goat Anti-Rabbit IgG (H+L) (AS011, ABclonal) and Cy3 Goat Anti-Mouse IgG (H+L) (AS008, ABclonal).

    Staining:

    Article Title: Macrophage-derived S100A9 promotes diabetic cardiomyopathy by disturbing mitochondrial quality control via STAT3 activation
    Article Snippet: .. After blocking in 1% goat serum for 1 hour at 37°C, staining was performed as above with anti-S100A9 (1:100 dilution, #73425, CST), anti-α-actinin (1:100 dilution, 66895-1-Ig, Proteintech), anti-CD11b (1:100 dilution, 66519-1-Ig, Proteintech), anti-CD80 (1:100 dilution, M1007-10, HUABIO), anti-F4/80 (1:100 dilution, P47789 , Abmart), and anti-CCR2 (1:100 dilution, TD7507M, Abmart) antibodies. .. Slides were washed and then incubated with FITC Goat Anti-Rabbit IgG (H+L) (AS011, ABclonal) and Cy3 Goat Anti-Mouse IgG (H+L) (AS008, ABclonal).

    Article Title: Macrophage-derived S100A9 promotes diabetic cardiomyopathy by disturbing mitochondrial quality control via STAT3 activation.
    Article Snippet: .. After blocking in 1% goat serum for 1 hour at 37°C, staining was performed as above with anti-S100A9 (1:100 dilution, #73425, CST), anti-α-actinin (1:100 dilution, 66895-1-Ig, Proteintech), anti-CD11b (1:100 dilution, 66519-1-Ig, Proteintech), anti-CD80 (1:100 dilution, M1007-10, HUABIO), anti-F4/80 (1:100 dilution, P47789, Abmart), and anti-CCR2 (1:100 dilution, TD7507M, Abmart) antibodies. .. Slides were washed and then incubated with FITC Goat Anti-Rabbit IgG (H+L) (AS011, ABclonal) and Cy3 Goat Anti-Mouse IgG (H+L) (AS008, ABclonal).



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    Image Search Results


    Characterization of Res-PD-L1@nmEVs . (A) Schematic illustration of the Res-PD-L1@nmEVs synthesis procedure. (B-D) Representative transmission electron microscopy (TEM) images, dynamic light scattering (DLS) size distributions, and zeta potential measurements of nEVs, PD-L1@mEVs, PD-L1@nmEVs, and Res-PD-L1@nmEVs. (E) PD-L1 expression in PD-L1-overexpressing MSCs (OE-PD-L1) and negative control (NC) MSCs, and CD11b expression in HL60 cells before and after DMSO stimulation, as determined by Western blot. (F) Expression levels of neutrophil membrane markers (CD11b, CXCR2, RAGE, TLR2) and the exosomal marker CD63 in the four EV types. (G) Fluorescence co-localization images of DiO-labeled nEVs (green) and DiL-labeled PD-L1@mEVs (red) after fusion, demonstrating hybrid vesicle formation. (H) Size stability of Res-PD-L1@nmEVs stored at 4 °C and 37 °C for 7 days. (I-K) Binding and neutralization capacity of Res-PD-L1@nmEVs against inflammatory cytokines (TNF-α, IL-6, IL-1β) in vitro. ∗ vs. 0ug/ml; # vs. 100 μg/ml, p < 0.05, n = 5.

    Journal: Bioactive Materials

    Article Title: Inhalable PD-L1-engineered hybrid cellular vesicles suppress excessive neutrophil activation and restore mitochondrial homeostasis to alleviate ischemia–reperfusion lung injury and pneumonia

    doi: 10.1016/j.bioactmat.2026.03.024

    Figure Lengend Snippet: Characterization of Res-PD-L1@nmEVs . (A) Schematic illustration of the Res-PD-L1@nmEVs synthesis procedure. (B-D) Representative transmission electron microscopy (TEM) images, dynamic light scattering (DLS) size distributions, and zeta potential measurements of nEVs, PD-L1@mEVs, PD-L1@nmEVs, and Res-PD-L1@nmEVs. (E) PD-L1 expression in PD-L1-overexpressing MSCs (OE-PD-L1) and negative control (NC) MSCs, and CD11b expression in HL60 cells before and after DMSO stimulation, as determined by Western blot. (F) Expression levels of neutrophil membrane markers (CD11b, CXCR2, RAGE, TLR2) and the exosomal marker CD63 in the four EV types. (G) Fluorescence co-localization images of DiO-labeled nEVs (green) and DiL-labeled PD-L1@mEVs (red) after fusion, demonstrating hybrid vesicle formation. (H) Size stability of Res-PD-L1@nmEVs stored at 4 °C and 37 °C for 7 days. (I-K) Binding and neutralization capacity of Res-PD-L1@nmEVs against inflammatory cytokines (TNF-α, IL-6, IL-1β) in vitro. ∗ vs. 0ug/ml; # vs. 100 μg/ml, p < 0.05, n = 5.

    Article Snippet: For detecting neutrophil characteristic proteins, the primary antibodies comprised CD11b (HA722075, HUABIO, China), CXCR2 (ER1906-87, HUABIO, China), RAGE (ET1702-27, HUABIO, China), TLR2 (ET1705-92, HUABIO, China), TNFR1(RT1624, HUABIO, China), IL6R ( AWA43078 , Abiowell, China) and the exosome marker CD63 (ET1607-2, HUABIO, China).

    Techniques: Transmission Assay, Electron Microscopy, Zeta Potential Analyzer, Expressing, Negative Control, Western Blot, Membrane, Marker, Fluorescence, Labeling, Binding Assay, Neutralization, In Vitro

    Res-PD-L1@nmEVs Suppresses Neutrophil Activation and Preserves Mitochondrial Integrity via PD-L1 Delivery (A-B) Rats subjected to lung IRI received nebulized administration of different formulations (Res, nEVs, PD-L1@mEVs, PD-L1@nmEVs, or Res-PD-L1@nmEVs) before ischemia and after reperfusion. Lung tissues were collected 2 h post-reperfusion. (A) Representative immunofluorescence images showing the expression and localization of CD11b (green), MPO (red), and PD-1 (yellow) in lung sections across treatment groups. (B) Enlarged view of the IRI group from (A). (C-D) mRNA levels of CD95 (C) and CD206 (D) in lung tissues. (E-F) Levels of myeloperoxidase (MPO) (E) and matrix metalloproteinase-9 (MMP-9) (F) in bronchoalveolar lavage fluid (BALF). (G-I) (G) Representative transmission electron microscopy (TEM) images of lung tissues (scale bar: 2 μm). (H) Proportion of damaged mitochondria. (I) Average number of mitophagic events per cell. (J) Immunofluorescence co-localization of mitochondrial marker TOMM20 (red) and EpCAM (green) in lung tissues (nuclei stained with DAPI, scale bar: 50 μm). (K-L) Protein expression levels of Beclin-1 (K) and LC3 (L) in lung tissues, with insets showing immunofluorescence co-localization of Beclin-1 (green) and LC3 (red) across treatment groups (nuclei stained with DAPI, scale bar: 50 μm). ∗ vs. Sham; # vs. IRI; & vs. IRI + PD-L1@nmEVs, p < 0.05.

    Journal: Bioactive Materials

    Article Title: Inhalable PD-L1-engineered hybrid cellular vesicles suppress excessive neutrophil activation and restore mitochondrial homeostasis to alleviate ischemia–reperfusion lung injury and pneumonia

    doi: 10.1016/j.bioactmat.2026.03.024

    Figure Lengend Snippet: Res-PD-L1@nmEVs Suppresses Neutrophil Activation and Preserves Mitochondrial Integrity via PD-L1 Delivery (A-B) Rats subjected to lung IRI received nebulized administration of different formulations (Res, nEVs, PD-L1@mEVs, PD-L1@nmEVs, or Res-PD-L1@nmEVs) before ischemia and after reperfusion. Lung tissues were collected 2 h post-reperfusion. (A) Representative immunofluorescence images showing the expression and localization of CD11b (green), MPO (red), and PD-1 (yellow) in lung sections across treatment groups. (B) Enlarged view of the IRI group from (A). (C-D) mRNA levels of CD95 (C) and CD206 (D) in lung tissues. (E-F) Levels of myeloperoxidase (MPO) (E) and matrix metalloproteinase-9 (MMP-9) (F) in bronchoalveolar lavage fluid (BALF). (G-I) (G) Representative transmission electron microscopy (TEM) images of lung tissues (scale bar: 2 μm). (H) Proportion of damaged mitochondria. (I) Average number of mitophagic events per cell. (J) Immunofluorescence co-localization of mitochondrial marker TOMM20 (red) and EpCAM (green) in lung tissues (nuclei stained with DAPI, scale bar: 50 μm). (K-L) Protein expression levels of Beclin-1 (K) and LC3 (L) in lung tissues, with insets showing immunofluorescence co-localization of Beclin-1 (green) and LC3 (red) across treatment groups (nuclei stained with DAPI, scale bar: 50 μm). ∗ vs. Sham; # vs. IRI; & vs. IRI + PD-L1@nmEVs, p < 0.05.

    Article Snippet: For detecting neutrophil characteristic proteins, the primary antibodies comprised CD11b (HA722075, HUABIO, China), CXCR2 (ER1906-87, HUABIO, China), RAGE (ET1702-27, HUABIO, China), TLR2 (ET1705-92, HUABIO, China), TNFR1(RT1624, HUABIO, China), IL6R ( AWA43078 , Abiowell, China) and the exosome marker CD63 (ET1607-2, HUABIO, China).

    Techniques: Activation Assay, Immunofluorescence, Expressing, Transmission Assay, Electron Microscopy, Marker, Staining