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anti cd68 primary antibody  (Bioss)


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    Structured Review

    Bioss anti cd68 primary antibody
    A HE: It can be seen that the cardiomyocytes in the model group are significantly enlarged and the nuclei become sparse. Sirius red staining: Some areas of myocardium in the model group showed an increase in cell spacing accompanied by fibrotic tissue metaplasia. In contrast, myocytes in the control group were neatly arranged and densely distributed, with significantly less fibrous tissue than in the model group. “LV”: left ventricle. “RV”: right ventricle. B In the model group, a small number of apoptotic cells were observed with green fluorescence, but no large aggregates were detected. C Additionally, there were numerous <t>CD68-positive</t> cells expressing red fluorescence, which were irregularly distributed on the cell wall and in the cytoplasm
    Anti Cd68 Primary Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 75 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+cd68+primary+antibody/CD68+Polyclonal+Antibody/pmc12858496-97-33-38
    Average 94 stars, based on 75 article reviews
    anti cd68 primary antibody - by Bioz Stars, 2026-10
    94/100 stars

    Images

    1) Product Images from "Extension of Atherosclerosis ApoE-/- Mouse—a Model of Chronic Myocardial Ischemia and Evaluation Method"

    Article Title: Extension of Atherosclerosis ApoE-/- Mouse—a Model of Chronic Myocardial Ischemia and Evaluation Method

    Journal: Journal of Cardiovascular Translational Research

    doi: 10.1007/s12265-025-10734-8

    A HE: It can be seen that the cardiomyocytes in the model group are significantly enlarged and the nuclei become sparse. Sirius red staining: Some areas of myocardium in the model group showed an increase in cell spacing accompanied by fibrotic tissue metaplasia. In contrast, myocytes in the control group were neatly arranged and densely distributed, with significantly less fibrous tissue than in the model group. “LV”: left ventricle. “RV”: right ventricle. B In the model group, a small number of apoptotic cells were observed with green fluorescence, but no large aggregates were detected. C Additionally, there were numerous CD68-positive cells expressing red fluorescence, which were irregularly distributed on the cell wall and in the cytoplasm
    Figure Legend Snippet: A HE: It can be seen that the cardiomyocytes in the model group are significantly enlarged and the nuclei become sparse. Sirius red staining: Some areas of myocardium in the model group showed an increase in cell spacing accompanied by fibrotic tissue metaplasia. In contrast, myocytes in the control group were neatly arranged and densely distributed, with significantly less fibrous tissue than in the model group. “LV”: left ventricle. “RV”: right ventricle. B In the model group, a small number of apoptotic cells were observed with green fluorescence, but no large aggregates were detected. C Additionally, there were numerous CD68-positive cells expressing red fluorescence, which were irregularly distributed on the cell wall and in the cytoplasm

    Techniques Used: Staining, Control, Fluorescence, Expressing

    Related Articles

    Blocking Assay:

    Article Title: Extension of Atherosclerosis ApoE-/- Mouse—a Model of Chronic Myocardial Ischemia and Evaluation Method
    Article Snippet: .. Tissue sections underwent blocking with 5% bovine serum albumin (BSA) (Sigma-Aldrich Cat# A7906) in PBST (0.1% Tween-20 in PBS) for 1 h at room temperature, followed by overnight incubation at 4 °C with anti-CD68 primary antibody (Rabbit polyclonal, Bioss Antibodies, Cat# bs-20403R, RRID: AB_10855800) diluted 1:100 in blocking solution. .. After three 5-min PBST washes, sections were incubated for 1 h with DyLight 594-conjugated goat anti-rabbit IgG (H + L) secondary antibody (Earthox, Cat# E032421, Lot# DL594-202,301) at 1:200 dilution.

    Incubation:

    Article Title: Extension of Atherosclerosis ApoE-/- Mouse—a Model of Chronic Myocardial Ischemia and Evaluation Method
    Article Snippet: .. Tissue sections underwent blocking with 5% bovine serum albumin (BSA) (Sigma-Aldrich Cat# A7906) in PBST (0.1% Tween-20 in PBS) for 1 h at room temperature, followed by overnight incubation at 4 °C with anti-CD68 primary antibody (Rabbit polyclonal, Bioss Antibodies, Cat# bs-20403R, RRID: AB_10855800) diluted 1:100 in blocking solution. .. After three 5-min PBST washes, sections were incubated for 1 h with DyLight 594-conjugated goat anti-rabbit IgG (H + L) secondary antibody (Earthox, Cat# E032421, Lot# DL594-202,301) at 1:200 dilution.



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    Pharmacology Network Analysis and Target Screening of YPFS. A Venn diagram depicting the overlap among survival-related genes, YPFS targets, and macrophage-associated genes, identifying AHSA1 as the intersection gene. B Network diagram showing relationships between active compounds and target genes. Green nodes represent target genes; red nodes, compounds from largehead atractylodes root; blue nodes, compounds from milkvetch root; and yellow nodes, compounds from divaricate saposhniovia root. C Interaction diagram illustrating AHSA1 and its targeting interactions with wogonin, kaempferol, and quercetin. D Kaplan–Meier survival curves of NSCLC patients stratified by high and low AHSA1 expression, showing poorer prognosis in the high-expression group. E Violin plot depicting AHSA1 expression across different cell types in single-cell data, with highest expression in epithelial cells. F Violin plot showing AHSA1 expression across macrophage functional subtypes, with peak expression observed in MAC3. G Violin plot comparing AHSA1 expression levels in macrophages from normal versus tumor tissues. H Tissue microarray immunofluorescence staining of AHSA1 and <t>CD68</t> in normal and tumor tissues. Scale bar, 50 μm
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    Image Search Results


    A HE: It can be seen that the cardiomyocytes in the model group are significantly enlarged and the nuclei become sparse. Sirius red staining: Some areas of myocardium in the model group showed an increase in cell spacing accompanied by fibrotic tissue metaplasia. In contrast, myocytes in the control group were neatly arranged and densely distributed, with significantly less fibrous tissue than in the model group. “LV”: left ventricle. “RV”: right ventricle. B In the model group, a small number of apoptotic cells were observed with green fluorescence, but no large aggregates were detected. C Additionally, there were numerous CD68-positive cells expressing red fluorescence, which were irregularly distributed on the cell wall and in the cytoplasm

    Journal: Journal of Cardiovascular Translational Research

    Article Title: Extension of Atherosclerosis ApoE-/- Mouse—a Model of Chronic Myocardial Ischemia and Evaluation Method

    doi: 10.1007/s12265-025-10734-8

    Figure Lengend Snippet: A HE: It can be seen that the cardiomyocytes in the model group are significantly enlarged and the nuclei become sparse. Sirius red staining: Some areas of myocardium in the model group showed an increase in cell spacing accompanied by fibrotic tissue metaplasia. In contrast, myocytes in the control group were neatly arranged and densely distributed, with significantly less fibrous tissue than in the model group. “LV”: left ventricle. “RV”: right ventricle. B In the model group, a small number of apoptotic cells were observed with green fluorescence, but no large aggregates were detected. C Additionally, there were numerous CD68-positive cells expressing red fluorescence, which were irregularly distributed on the cell wall and in the cytoplasm

    Article Snippet: Tissue sections underwent blocking with 5% bovine serum albumin (BSA) (Sigma-Aldrich Cat# A7906) in PBST (0.1% Tween-20 in PBS) for 1 h at room temperature, followed by overnight incubation at 4 °C with anti-CD68 primary antibody (Rabbit polyclonal, Bioss Antibodies, Cat# bs-20403R, RRID: AB_10855800) diluted 1:100 in blocking solution.

    Techniques: Staining, Control, Fluorescence, Expressing

    Pharmacology Network Analysis and Target Screening of YPFS. A Venn diagram depicting the overlap among survival-related genes, YPFS targets, and macrophage-associated genes, identifying AHSA1 as the intersection gene. B Network diagram showing relationships between active compounds and target genes. Green nodes represent target genes; red nodes, compounds from largehead atractylodes root; blue nodes, compounds from milkvetch root; and yellow nodes, compounds from divaricate saposhniovia root. C Interaction diagram illustrating AHSA1 and its targeting interactions with wogonin, kaempferol, and quercetin. D Kaplan–Meier survival curves of NSCLC patients stratified by high and low AHSA1 expression, showing poorer prognosis in the high-expression group. E Violin plot depicting AHSA1 expression across different cell types in single-cell data, with highest expression in epithelial cells. F Violin plot showing AHSA1 expression across macrophage functional subtypes, with peak expression observed in MAC3. G Violin plot comparing AHSA1 expression levels in macrophages from normal versus tumor tissues. H Tissue microarray immunofluorescence staining of AHSA1 and CD68 in normal and tumor tissues. Scale bar, 50 μm

    Journal: Cancer Immunology, Immunotherapy : CII

    Article Title: Single-cell sequencing and network pharmacology coupled with molecular docking and experimental validation reveal the effects of YPFS on macrophages in stage I non-small cell lung cancer

    doi: 10.1007/s00262-026-04305-2

    Figure Lengend Snippet: Pharmacology Network Analysis and Target Screening of YPFS. A Venn diagram depicting the overlap among survival-related genes, YPFS targets, and macrophage-associated genes, identifying AHSA1 as the intersection gene. B Network diagram showing relationships between active compounds and target genes. Green nodes represent target genes; red nodes, compounds from largehead atractylodes root; blue nodes, compounds from milkvetch root; and yellow nodes, compounds from divaricate saposhniovia root. C Interaction diagram illustrating AHSA1 and its targeting interactions with wogonin, kaempferol, and quercetin. D Kaplan–Meier survival curves of NSCLC patients stratified by high and low AHSA1 expression, showing poorer prognosis in the high-expression group. E Violin plot depicting AHSA1 expression across different cell types in single-cell data, with highest expression in epithelial cells. F Violin plot showing AHSA1 expression across macrophage functional subtypes, with peak expression observed in MAC3. G Violin plot comparing AHSA1 expression levels in macrophages from normal versus tumor tissues. H Tissue microarray immunofluorescence staining of AHSA1 and CD68 in normal and tumor tissues. Scale bar, 50 μm

    Article Snippet: Staining was performed with the Tyramide Signal Amplification (TSA) kit (ABclonal, CAT #RK05902) using primary antibodies against CD68 (ABclonal, CAT #A20803) and AHSA1 (Invitrogen, CAT #PA5-27672), according to the manufacturer’s instructions.

    Techniques: Expressing, Functional Assay, Microarray, Immunofluorescence, Staining