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mouse ccl3 mip 1a elisa kit  (Multi Sciences (Lianke) Biotech Co Ltd)


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    Multi Sciences (Lianke) Biotech Co Ltd mouse ccl3 mip 1a elisa kit
    Mouse Ccl3 Mip 1a Elisa Kit, supplied by Multi Sciences (Lianke) Biotech Co Ltd, used in various techniques. Bioz Stars score: 94/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse ccl3 mip 1a elisa kit/product/Multi Sciences (Lianke) Biotech Co Ltd
    Average 94 stars, based on 9 article reviews
    mouse ccl3 mip 1a elisa kit - by Bioz Stars, 2026-02
    94/100 stars

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    Multi Sciences (Lianke) Biotech Co Ltd ccl3 protein level
    a Western blot shows the efficient depletion of SATB1 in CD4 + T cells. b A representative mouse from each group is photographed (6–16 weeks male mice). c Statistical comparison of quantified body weight among Ctrl and Satb1 cKO mice (6–16 weeks male mice, n = 10 for each group). Error bars indicate Mean ± SD and each dot represents a mouse. Statistical significance is measured via paired Student’s t-tests and is presented as follows: *** p < 0.005. d Volcano plot shows the 365 significantly down-regulated (log2FC < −1 and padj < 0.05) and 794 significantly up-regulated (log2FC > 1 and padj < 0.05) genes in activated naive CD4 + T cells of Ctrl and Satb1 cKO. About 6–16 weeks male mice were used in this experiment and each group had 3 independent biological replicates. e Dot plots indicate the top 5 most enriched BP (biological process) GO terms in up-regulated genes identified in ( a ). f Heatmaps of <t>Ccl3</t> , Ccl4, Ccl5, Ccl6 and Ccl9 genes. Each column shows the scaled gene expression in an RNA-Seq replicate, each row represents a gene. g Violin plots of differentially expressed genes in each chemokine family. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. h , i Immunohistochemical stainings for CD4 and CCL3 in lung tissues for each group. The representative image shows the lung infiltrating immune cells expressing CD4 and CCL3. j Flow cytometric sorting strategy for CD4 + T cells in lung tissues. The lung tissues were digested into single-cell suspension and stained CD4 antibodies for flow cytometric sorting. k Protein levels of chemokine CCL3 in lung-infiltrating T cells (sorted from ( g )) were measured using ELISA ( n = 3). Statistical significance is measured via unpaired Student’s t-tests and is presented as *** p < 0.005.
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    Multi Sciences (Lianke) Biotech Co Ltd mouse ccl3 mip 1α elisa kit
    a Western blot shows the efficient depletion of SATB1 in CD4 + T cells. b A representative mouse from each group is photographed (6–16 weeks male mice). c Statistical comparison of quantified body weight among Ctrl and Satb1 cKO mice (6–16 weeks male mice, n = 10 for each group). Error bars indicate Mean ± SD and each dot represents a mouse. Statistical significance is measured via paired Student’s t-tests and is presented as follows: *** p < 0.005. d Volcano plot shows the 365 significantly down-regulated (log2FC < −1 and padj < 0.05) and 794 significantly up-regulated (log2FC > 1 and padj < 0.05) genes in activated naive CD4 + T cells of Ctrl and Satb1 cKO. About 6–16 weeks male mice were used in this experiment and each group had 3 independent biological replicates. e Dot plots indicate the top 5 most enriched BP (biological process) GO terms in up-regulated genes identified in ( a ). f Heatmaps of <t>Ccl3</t> , Ccl4, Ccl5, Ccl6 and Ccl9 genes. Each column shows the scaled gene expression in an RNA-Seq replicate, each row represents a gene. g Violin plots of differentially expressed genes in each chemokine family. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. h , i Immunohistochemical stainings for CD4 and CCL3 in lung tissues for each group. The representative image shows the lung infiltrating immune cells expressing CD4 and CCL3. j Flow cytometric sorting strategy for CD4 + T cells in lung tissues. The lung tissues were digested into single-cell suspension and stained CD4 antibodies for flow cytometric sorting. k Protein levels of chemokine CCL3 in lung-infiltrating T cells (sorted from ( g )) were measured using ELISA ( n = 3). Statistical significance is measured via unpaired Student’s t-tests and is presented as *** p < 0.005.
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    https://www.bioz.com/result/mouse ccl3 mip 1α elisa kit/product/Multi Sciences (Lianke) Biotech Co Ltd
    Average 94 stars, based on 1 article reviews
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      Buy from Supplier

    Image Search Results


    a Western blot shows the efficient depletion of SATB1 in CD4 + T cells. b A representative mouse from each group is photographed (6–16 weeks male mice). c Statistical comparison of quantified body weight among Ctrl and Satb1 cKO mice (6–16 weeks male mice, n = 10 for each group). Error bars indicate Mean ± SD and each dot represents a mouse. Statistical significance is measured via paired Student’s t-tests and is presented as follows: *** p < 0.005. d Volcano plot shows the 365 significantly down-regulated (log2FC < −1 and padj < 0.05) and 794 significantly up-regulated (log2FC > 1 and padj < 0.05) genes in activated naive CD4 + T cells of Ctrl and Satb1 cKO. About 6–16 weeks male mice were used in this experiment and each group had 3 independent biological replicates. e Dot plots indicate the top 5 most enriched BP (biological process) GO terms in up-regulated genes identified in ( a ). f Heatmaps of Ccl3 , Ccl4, Ccl5, Ccl6 and Ccl9 genes. Each column shows the scaled gene expression in an RNA-Seq replicate, each row represents a gene. g Violin plots of differentially expressed genes in each chemokine family. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. h , i Immunohistochemical stainings for CD4 and CCL3 in lung tissues for each group. The representative image shows the lung infiltrating immune cells expressing CD4 and CCL3. j Flow cytometric sorting strategy for CD4 + T cells in lung tissues. The lung tissues were digested into single-cell suspension and stained CD4 antibodies for flow cytometric sorting. k Protein levels of chemokine CCL3 in lung-infiltrating T cells (sorted from ( g )) were measured using ELISA ( n = 3). Statistical significance is measured via unpaired Student’s t-tests and is presented as *** p < 0.005.

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: a Western blot shows the efficient depletion of SATB1 in CD4 + T cells. b A representative mouse from each group is photographed (6–16 weeks male mice). c Statistical comparison of quantified body weight among Ctrl and Satb1 cKO mice (6–16 weeks male mice, n = 10 for each group). Error bars indicate Mean ± SD and each dot represents a mouse. Statistical significance is measured via paired Student’s t-tests and is presented as follows: *** p < 0.005. d Volcano plot shows the 365 significantly down-regulated (log2FC < −1 and padj < 0.05) and 794 significantly up-regulated (log2FC > 1 and padj < 0.05) genes in activated naive CD4 + T cells of Ctrl and Satb1 cKO. About 6–16 weeks male mice were used in this experiment and each group had 3 independent biological replicates. e Dot plots indicate the top 5 most enriched BP (biological process) GO terms in up-regulated genes identified in ( a ). f Heatmaps of Ccl3 , Ccl4, Ccl5, Ccl6 and Ccl9 genes. Each column shows the scaled gene expression in an RNA-Seq replicate, each row represents a gene. g Violin plots of differentially expressed genes in each chemokine family. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. h , i Immunohistochemical stainings for CD4 and CCL3 in lung tissues for each group. The representative image shows the lung infiltrating immune cells expressing CD4 and CCL3. j Flow cytometric sorting strategy for CD4 + T cells in lung tissues. The lung tissues were digested into single-cell suspension and stained CD4 antibodies for flow cytometric sorting. k Protein levels of chemokine CCL3 in lung-infiltrating T cells (sorted from ( g )) were measured using ELISA ( n = 3). Statistical significance is measured via unpaired Student’s t-tests and is presented as *** p < 0.005.

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques: Western Blot, Comparison, Gene Expression, RNA Sequencing, Immunohistochemical staining, Expressing, Suspension, Staining, Enzyme-linked Immunosorbent Assay

    a Principle component analysis (PCA) of the samples used for H3K27ac CUT&Tag analysis. b Heatmap displaying the correlation of H3K27ac CUT&Tag experiments replicates. c Volcano plot showing 8561 differential H3K27ac peaks (4694 up-regulated in red and 3861 down-regulated in blue) between Satb1 cKO and control mice. d Boxplot compares expression changes for genes adjacent to H3K27ac peaks. Genes with peaks of H3K27ac in their promoter regions are classified as genes adjacent to H3K27ac peaks. The median values (-0.195, 0.109, 0.016) are displayed on top of the graphs. e H3K27ac signals on the gene cluster sites of Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 are visualized by IGV software. No significant change was observed in the H3K27ac levels at these sites, while a noticeable enhancer site was identified in the middle of the gene loci of Ccl3 and Ccl6 , named as Ccl -Enhancer, which was labeled in the gray box.

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: a Principle component analysis (PCA) of the samples used for H3K27ac CUT&Tag analysis. b Heatmap displaying the correlation of H3K27ac CUT&Tag experiments replicates. c Volcano plot showing 8561 differential H3K27ac peaks (4694 up-regulated in red and 3861 down-regulated in blue) between Satb1 cKO and control mice. d Boxplot compares expression changes for genes adjacent to H3K27ac peaks. Genes with peaks of H3K27ac in their promoter regions are classified as genes adjacent to H3K27ac peaks. The median values (-0.195, 0.109, 0.016) are displayed on top of the graphs. e H3K27ac signals on the gene cluster sites of Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 are visualized by IGV software. No significant change was observed in the H3K27ac levels at these sites, while a noticeable enhancer site was identified in the middle of the gene loci of Ccl3 and Ccl6 , named as Ccl -Enhancer, which was labeled in the gray box.

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques: Control, Expressing, Software, Labeling

    a Hi-C heatmaps at 10 kb resolution show changed chromatin interactions at Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 gene loci in thymic T cells. CUT&Tag profiles show the SATB1 and CTCF signals in control and Satb1 cKO thymocyte cells. The Ccl -Enhancer was labeled in the gray box. b Diagram depicting the regions of subTAD and adjacent and boxplot showing the interaction frequencies of different regions indicated in ( a ). The adjacent region was set as an internal reference. Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. c The diagram depicted the 3C-qPCR experiment design and the 3C-qPCR experiment was used to validate the enhancer-promoter interaction of Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 genes in both control and Satb1 cKO naive CD4 + T cells. A negative control was also detected. Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. d dCas9 experiment was performed to validate the function of enhancer-promoter interaction in the regulation of gene expression for Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 . Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005.

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: a Hi-C heatmaps at 10 kb resolution show changed chromatin interactions at Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 gene loci in thymic T cells. CUT&Tag profiles show the SATB1 and CTCF signals in control and Satb1 cKO thymocyte cells. The Ccl -Enhancer was labeled in the gray box. b Diagram depicting the regions of subTAD and adjacent and boxplot showing the interaction frequencies of different regions indicated in ( a ). The adjacent region was set as an internal reference. Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. c The diagram depicted the 3C-qPCR experiment design and the 3C-qPCR experiment was used to validate the enhancer-promoter interaction of Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 genes in both control and Satb1 cKO naive CD4 + T cells. A negative control was also detected. Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005. d dCas9 experiment was performed to validate the function of enhancer-promoter interaction in the regulation of gene expression for Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 . Error bars indicate Mean ± SD. Statistical significance is measured via unpaired Student’s t-tests and is presented as follows: * p < 0.05, ** p < 0.01, *** p < 0.005.

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques: Hi-C, Control, Labeling, Negative Control, Gene Expression

    SATB1 inhibited Ccl gene expression by restraining enhancer-promoter interaction. The loss of SATB1 led to the emergence of a new chromatin domain encompassing the Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 genes and a distal enhancer, which possibly mediated by CTCF, resulting in increased contacts between the enhancer and all five chemokine genes, thus inducing autoimmunity.

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: SATB1 inhibited Ccl gene expression by restraining enhancer-promoter interaction. The loss of SATB1 led to the emergence of a new chromatin domain encompassing the Ccl3, Ccl4, Ccl5, Ccl6 , and Ccl9 genes and a distal enhancer, which possibly mediated by CTCF, resulting in increased contacts between the enhancer and all five chemokine genes, thus inducing autoimmunity.

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques: Gene Expression

    Primers for RT-qPCR

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: Primers for RT-qPCR

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques:

    Primers for 3C-qPCR

    Journal: Communications Biology

    Article Title: SATB1 prevents immune cell infiltration by regulating chromatin organization and gene expression of a chemokine gene cluster in T cells

    doi: 10.1038/s42003-024-07021-8

    Figure Lengend Snippet: Primers for 3C-qPCR

    Article Snippet: CCL3 protein level was determined using Mouse CCL3/MIP-1α ELISA Kit (Liankebio, EK261) according to the manufacturer’s instructions.

    Techniques: Control, Negative Control