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antibody against cd68 ba3638  (Boster Bio)


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    Boster Bio antibody against cd68 ba3638
    Antibody Against Cd68 Ba3638, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 284 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antibody against cd68 ba3638/product/Boster Bio
    Average 96 stars, based on 284 article reviews
    antibody against cd68 ba3638 - by Bioz Stars, 2026-03
    96/100 stars

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    MVP positively correlates with <t>CD68</t> + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="250" height="auto" />
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    MVP positively correlates with <t>CD68</t> + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="250" height="auto" />
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    MVP positively correlates with <t>CD68</t> + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="250" height="auto" />
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    MVP positively correlates with <t>CD68</t> + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="250" height="auto" />
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    MVP positively correlates with <t>CD68</t> + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="250" height="auto" />
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    cd68 ba3638  (Boster Bio)
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    Boster Bio cd68 ba3638
    Immunohistochemistry staining of wound tissues on days 7 and 14. (A) Representative images for CD31, PCNA, α-SMA, and <t>CD68</t> staining (scale bar = 100 μm). (B–E) Quantification of CD31, PCNA, α-SMA, and CD68 protein expressions, respectively. * p < 0.05, ** p < 0.01, *** p < 0.001 vs . control group; # p < 0.05, ## p < 0.01, ### p < 0.001 vs . CAH group as statistically significant.
    Cd68 Ba3638, supplied by Boster Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    MVP positively correlates with CD68 + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also <xref ref-type= Supplementary Figures 1 and 2 . " width="100%" height="100%">

    Journal: Frontiers in Immunology

    Article Title: Major vault protein regulates tumor-associated macrophage polarization through interaction with signal transducer and activator of transcription 6

    doi: 10.3389/fimmu.2023.1289795

    Figure Lengend Snippet: MVP positively correlates with CD68 + /Arg-1 + /CD206 + TAMs in HCC samples. (A) The histogram of Rho between MVP expression and 22 types of immune cell infiltration levels in LIHC from the TIMER2.0 database. The red box highlights the immune cells with the highest positive correlation. (B) The scatter plot of the correlation between MVP expression level with tumor purity and M2 macrophage infiltration level determined by the TIMER2.0. TPM: Transcripts Per Kilobase of exon model per Million mapped reads. (C–E) Immunofluorescence representative images and co-localization quantitative analysis of MVP (green) with CD68 (red) (C) , MVP (green) with Arg-1 (red) (D) , and MVP (green) with CD206 (red) (E) in adjacent nontumorous tissues (ANT) and HCC tumor tissues (n=10). Scale bar, 100 µm (MVP/CD68/Arg-1/CD206/Merge) and 20 µm (Zoom in). All levels of co-localization are indicated by Pearson’s correlation coefficients calculated using Image J. Data are expressed as means ± SEM, two-tailed Student’s t-test, (***P < 0.001, **P < 0.01, *P < 0.05, ns, no significance). See also Supplementary Figures 1 and 2 .

    Article Snippet: The antibody for CD68 (BA3638) was purchased from Boster Biological Technology.

    Techniques: Expressing, Immunofluorescence, Two Tailed Test

    Immunohistochemistry staining of wound tissues on days 7 and 14. (A) Representative images for CD31, PCNA, α-SMA, and CD68 staining (scale bar = 100 μm). (B–E) Quantification of CD31, PCNA, α-SMA, and CD68 protein expressions, respectively. * p < 0.05, ** p < 0.01, *** p < 0.001 vs . control group; # p < 0.05, ## p < 0.01, ### p < 0.001 vs . CAH group as statistically significant.

    Journal: Frontiers in Pharmacology

    Article Title: Chitosan/Sodium Alginate/Velvet Antler Blood Peptides Hydrogel Promoted Wound Healing by Regulating PI3K/AKT/mTOR and SIRT1/NF-κB Pathways

    doi: 10.3389/fphar.2022.913408

    Figure Lengend Snippet: Immunohistochemistry staining of wound tissues on days 7 and 14. (A) Representative images for CD31, PCNA, α-SMA, and CD68 staining (scale bar = 100 μm). (B–E) Quantification of CD31, PCNA, α-SMA, and CD68 protein expressions, respectively. * p < 0.05, ** p < 0.01, *** p < 0.001 vs . control group; # p < 0.05, ## p < 0.01, ### p < 0.001 vs . CAH group as statistically significant.

    Article Snippet: The primary antibody against CD31 (ab182981) came from Abcam (Cambridge, United Kingdom); PCNA (BM0104), α-SMA (BM0002), and CD68 (BA3638) were from BOSTER (Wuhan, China); p-PI3K (#4228) was from Cell Signaling Technology (Beverly, MA, United States); p-AKT (ARG51559) and p-mTOR (ARG40666) were acquired from Arigo (Hsinchu, Taiwan, China); and PI3K (67071-1-lg), AKT (60203-2-lg), mTOR (10745-1-AP), SIRT1 (13161-1-AP), NF-κB (p65, 10745-1-AP), IL-1β (26048-1-AP), TNF-α (17590-1-AP), β-actin (66009-1-lg), and horseradish peroxidase (HRP)–conjugated second antibodies (SA00001-1/SA00001-2) were purchased from Proteintech Group (Chicago, IL, United States).

    Techniques: Immunohistochemistry, Staining, Control