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biotinylated mouse mabs anti-human c4 (anti-c4)  (BioPorto Inc)

 
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    BioPorto Inc biotinylated mouse mabs anti-human c4 (anti-c4)
    Biotinylated Mouse Mabs Anti Human C4 (Anti C4), supplied by BioPorto 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/product/mouse+anti-human+c4+mab/biotinylated+anti+c4+antibody+hyb+162+2/pmc06120983-75-9-15
    Average 90 stars, based on 1 article reviews
    biotinylated mouse mabs anti-human c4 (anti-c4) - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Specific serum Ig recognizing staphylococcal wall teichoic acid induces complement-mediated opsonophagocytosis against Staphylococcus aureus.
    Article Snippet: To detect bound C4b, we used mouse anti-human C4 mAb (diluted 1:500; Bioporto) and goat F(ab9)2 anti-mouse IgG mAb conjugated with FITC (diluted 1:200; Beckman Coulter).

    Article Title: Glycoepitopes of Staphylococcal Wall Teichoic Acid Govern Complement-mediated Opsonophagocytosis via Human Serum Antibody and Mannose-binding Lectin
    Article Snippet: To detect bound C4b, mouse anti-human C4 mAb (Bioporto; diluted 1:500) was used.

    Article Title: Glycoepitopes of Staphylococcal Wall Teichoic Acid Govern Complement-mediated Opsonophagocytosis via Human Serum Antibody and Mannose-binding Lectin
    Article Snippet: To detect bound C4b, mouse anti-human C4 mAb (Bioporto; diluted 1:500) was used.



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    Image Search Results


    Complement component C4 and C5 expression in WT and Mdr2-KO mouse livers. (A) Liver sections were stained with Clec4f (green) for KCs, C4 (red), and DAPI for nuclei (blue). Dotted lines demarcate Clecf + cells as well as immune cell infiltrates in portal triads from adjacent liver parenchyma. (B) Liver sections were stained with Clec4f (green) for KCs, C5 (red), and DAPI (blue) for nuclei. (C) Complement component C3, C1q, CD68 expression in WT and Mdr2-KO livers. Liver sections were stained with C3 (red), C1q (white), and CD68 (green) for macrophages/KCs and DAPI for nuclei (blue). Dotted lines demarcate immune cell infiltration sites from adjacent liver parenchyma. White squares represent high magnification images shown separately. Representative images of WT livers (n=6); Mdr2-KO livers (n=6) are shown. Scale bars 100 μm in images of low and high magnification.

    Journal: Frontiers in Immunology

    Article Title: The C1q-ApoE complex: A new hallmark pathology of viral hepatitis and nonalcoholic fatty liver disease

    doi: 10.3389/fimmu.2022.970938

    Figure Lengend Snippet: Complement component C4 and C5 expression in WT and Mdr2-KO mouse livers. (A) Liver sections were stained with Clec4f (green) for KCs, C4 (red), and DAPI for nuclei (blue). Dotted lines demarcate Clecf + cells as well as immune cell infiltrates in portal triads from adjacent liver parenchyma. (B) Liver sections were stained with Clec4f (green) for KCs, C5 (red), and DAPI (blue) for nuclei. (C) Complement component C3, C1q, CD68 expression in WT and Mdr2-KO livers. Liver sections were stained with C3 (red), C1q (white), and CD68 (green) for macrophages/KCs and DAPI for nuclei (blue). Dotted lines demarcate immune cell infiltration sites from adjacent liver parenchyma. White squares represent high magnification images shown separately. Representative images of WT livers (n=6); Mdr2-KO livers (n=6) are shown. Scale bars 100 μm in images of low and high magnification.

    Article Snippet: Immunoflorescent (IF) stainings of mouse liver sections were performed using the following primary antibodies: anti-mouse/human ApoE (ab52607; Abcam); anti-mouse C1q (ab182451; Abcam); anti-mouse CLEC4F (ab2608299; Invitrogen); anti-mouse CD68 (FA11; Serotec); anti-mouse CD31 (ab553370; BD PharMingen); anti-human C3 (A213; ComplementTech); anti-mouse C4 (HM1046; Hycult Biotech); anti-mouse C5 (ab11898, Abcam).

    Techniques: Expressing, Staining

    Transcript expression of C1q, ApoE and complement components in KCs and hepatocytes in healthy and diseased mouse livers. (A, B) Violin plots show C1qa, C1qb, C1qc, ApoE (A) and C4b, C3, and C5 (B) transcripts in KCs in standard diet-fed or WD-fed mice for 24 and 36 weeks. (C, D) Violin plots show C1qa, C1qb, C1qc, ApoE (C) and C4b, C3, and C5 (D) transcripts in hepatocytes in healthy and diseased mice. (E, F) Violin plots show CD55, C5AR1 and C5AR2 transcripts in KCs (E) and hepatocytes (F) in healthy and diseased mice. Each point represents one cell. Kruskal–Walli’s test with Dunn’s non-parametric all-pairs comparison test was adjusted by Benjamini Hochberg correction. *P < 0.05; **P < 0.01; ***P < 0.001.

    Journal: Frontiers in Immunology

    Article Title: The C1q-ApoE complex: A new hallmark pathology of viral hepatitis and nonalcoholic fatty liver disease

    doi: 10.3389/fimmu.2022.970938

    Figure Lengend Snippet: Transcript expression of C1q, ApoE and complement components in KCs and hepatocytes in healthy and diseased mouse livers. (A, B) Violin plots show C1qa, C1qb, C1qc, ApoE (A) and C4b, C3, and C5 (B) transcripts in KCs in standard diet-fed or WD-fed mice for 24 and 36 weeks. (C, D) Violin plots show C1qa, C1qb, C1qc, ApoE (C) and C4b, C3, and C5 (D) transcripts in hepatocytes in healthy and diseased mice. (E, F) Violin plots show CD55, C5AR1 and C5AR2 transcripts in KCs (E) and hepatocytes (F) in healthy and diseased mice. Each point represents one cell. Kruskal–Walli’s test with Dunn’s non-parametric all-pairs comparison test was adjusted by Benjamini Hochberg correction. *P < 0.05; **P < 0.01; ***P < 0.001.

    Article Snippet: Immunoflorescent (IF) stainings of mouse liver sections were performed using the following primary antibodies: anti-mouse/human ApoE (ab52607; Abcam); anti-mouse C1q (ab182451; Abcam); anti-mouse CLEC4F (ab2608299; Invitrogen); anti-mouse CD68 (FA11; Serotec); anti-mouse CD31 (ab553370; BD PharMingen); anti-human C3 (A213; ComplementTech); anti-mouse C4 (HM1046; Hycult Biotech); anti-mouse C5 (ab11898, Abcam).

    Techniques: Expressing

    Expression of C1q, ApoE, and complement components in KCs and hepatocytes in human livers. (A, B) Violin plots show C1qa, C1qb, C1qc, and ApoE transcripts (A) and C2, C3, and C5 transcripts in KCs (B) in human livers. (C, D) Violin plots show C1qa, C1qb, C1qc, and ApoE transcripts (C) and C2, C3, and C5 transcripts in hepatocytes (D) in healthy and diseased livers. (E, F) Violin plots show CD55, C5AR1 and C5AR2 transcripts in KCs (E) and hepatocytes (F) in healthy and diseased human livers. Each point represents one cell. Data were analyzed by Wilcoxon rank sum test. P values were adjusted by Benjamini Hochberg correction. *P < 0.05, ***P < 0.001.

    Journal: Frontiers in Immunology

    Article Title: The C1q-ApoE complex: A new hallmark pathology of viral hepatitis and nonalcoholic fatty liver disease

    doi: 10.3389/fimmu.2022.970938

    Figure Lengend Snippet: Expression of C1q, ApoE, and complement components in KCs and hepatocytes in human livers. (A, B) Violin plots show C1qa, C1qb, C1qc, and ApoE transcripts (A) and C2, C3, and C5 transcripts in KCs (B) in human livers. (C, D) Violin plots show C1qa, C1qb, C1qc, and ApoE transcripts (C) and C2, C3, and C5 transcripts in hepatocytes (D) in healthy and diseased livers. (E, F) Violin plots show CD55, C5AR1 and C5AR2 transcripts in KCs (E) and hepatocytes (F) in healthy and diseased human livers. Each point represents one cell. Data were analyzed by Wilcoxon rank sum test. P values were adjusted by Benjamini Hochberg correction. *P < 0.05, ***P < 0.001.

    Article Snippet: Immunoflorescent (IF) stainings of mouse liver sections were performed using the following primary antibodies: anti-mouse/human ApoE (ab52607; Abcam); anti-mouse C1q (ab182451; Abcam); anti-mouse CLEC4F (ab2608299; Invitrogen); anti-mouse CD68 (FA11; Serotec); anti-mouse CD31 (ab553370; BD PharMingen); anti-human C3 (A213; ComplementTech); anti-mouse C4 (HM1046; Hycult Biotech); anti-mouse C5 (ab11898, Abcam).

    Techniques: Expressing

    BLU expression downregulates cyclin D1 promoter and JNK activity, and inhibits phosphorylation of c-Jun . ( A ) CNE-2 cells were transfected with pCD316 vector or pCD316- BLU , and cell lysates were immunoblotted and probed with goat anti-human BLU polyclonal antibody. The membranes were stripped and re-probed with anti-actin mAb clone C4. ( B ) Expression of BLU inhibits cyclin D1 promoter activity. pCD316 and pCD316p- BLU plasmids were co-transfected with cyclin D1 promoter reporter at concentration ratios of 1:1.5 and 1:4, respectively. The luciferase activity was measured for the two conditions, and the reporter activity was presented as the ratio of the two. The data are presented as the mean ± SD, and are derived from at least three independent tests. *Indicates t < 0.05 when compared with the measured values from the two groups. ( C ) pCD316- BLU and empty vector were co-transfected with JNK reporter at concentration ratios of 1:1.5 and 1:4, and the reporter activity was calculated. The data re presented as mean ± SD, and were derived from at least three independent tests. *Indicates P < 0.05 when comparing the calculated values for the relative light units between the two groups. ( D ) CNE-2 cells were infected with 0, 10, 50 and 100 PFU Ad BLU (lanes 1, 2, 3, 4), and ectopic expression was demonstrated by immunoblotting and probing with anti BLU goat polyclonal, anti actin mAb, anti phospho-c-Jun (P-c-Jun) and anti-c-Jun rabbit polyclonal antibodies. c-Jun phosphorylation was inhibited by infection with 100 PFU Ad BLU .

    Journal: BMC Cancer

    Article Title: Tumor suppressor BLU inhibits proliferation of nasopharyngeal carcinoma cells by regulation of cell cycle, c-Jun N-terminal kinase and the cyclin D1 promoter

    doi: 10.1186/1471-2407-12-267

    Figure Lengend Snippet: BLU expression downregulates cyclin D1 promoter and JNK activity, and inhibits phosphorylation of c-Jun . ( A ) CNE-2 cells were transfected with pCD316 vector or pCD316- BLU , and cell lysates were immunoblotted and probed with goat anti-human BLU polyclonal antibody. The membranes were stripped and re-probed with anti-actin mAb clone C4. ( B ) Expression of BLU inhibits cyclin D1 promoter activity. pCD316 and pCD316p- BLU plasmids were co-transfected with cyclin D1 promoter reporter at concentration ratios of 1:1.5 and 1:4, respectively. The luciferase activity was measured for the two conditions, and the reporter activity was presented as the ratio of the two. The data are presented as the mean ± SD, and are derived from at least three independent tests. *Indicates t < 0.05 when compared with the measured values from the two groups. ( C ) pCD316- BLU and empty vector were co-transfected with JNK reporter at concentration ratios of 1:1.5 and 1:4, and the reporter activity was calculated. The data re presented as mean ± SD, and were derived from at least three independent tests. *Indicates P < 0.05 when comparing the calculated values for the relative light units between the two groups. ( D ) CNE-2 cells were infected with 0, 10, 50 and 100 PFU Ad BLU (lanes 1, 2, 3, 4), and ectopic expression was demonstrated by immunoblotting and probing with anti BLU goat polyclonal, anti actin mAb, anti phospho-c-Jun (P-c-Jun) and anti-c-Jun rabbit polyclonal antibodies. c-Jun phosphorylation was inhibited by infection with 100 PFU Ad BLU .

    Article Snippet: Mouse anti-human actin monoclonal antibody (mAB) and clone C4 was purchased from Millipore (Beijing, China).

    Techniques: Expressing, Activity Assay, Phospho-proteomics, Transfection, Plasmid Preparation, Concentration Assay, Luciferase, Derivative Assay, Infection, Western Blot