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mouse anti rat cd11c alexa fluor 647 antibody  (Bio-Rad)


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    Structured Review

    Bio-Rad mouse anti rat cd11c alexa fluor 647 antibody
    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against <t>CD11c</t> (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.
    Mouse Anti Rat Cd11c Alexa Fluor 647 Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+rat+cd11c+alexa+fluor+647+antibody/Mouse+anti+Rat+CD63%3AAlexa+Fluor+647/pm20584093-77-9-14
    Average 93 stars, based on 23 article reviews
    mouse anti rat cd11c alexa fluor 647 antibody - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Characterization of dendritic cells in testicular draining lymph nodes in a rat model of experimental autoimmune orchitis."

    Article Title: Characterization of dendritic cells in testicular draining lymph nodes in a rat model of experimental autoimmune orchitis.

    Journal: International journal of andrology

    doi: 10.1111/j.1365-2605.2010.01082.x

    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against CD11c (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.
    Figure Legend Snippet: Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against CD11c (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.

    Techniques Used: Magnetic Beads, Suspension, Immunopeptidomics



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    mouse anti rat cd11c alexa fluor 647 antibody  (Bio-Rad)
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    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against <t>CD11c</t> (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.
    Mouse Anti Rat Cd11c Alexa Fluor 647 Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+rat+cd11c+alexa+fluor+647+antibody/Mouse+anti+Rat+CD63%3AAlexa+Fluor+647/pm20584093-77-9-14
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    mouse anti rat cd11c alexa fluor 647 antibody - by Bioz Stars, 2026-09
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    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against <t>CD11c</t> (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.
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    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against <t>CD11c</t> (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.
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    Image Search Results


    Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against CD11c (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.

    Journal: International journal of andrology

    Article Title: Characterization of dendritic cells in testicular draining lymph nodes in a rat model of experimental autoimmune orchitis.

    doi: 10.1111/j.1365-2605.2010.01082.x

    Figure Lengend Snippet: Figure 1 Flow cytometric characterization of the dendritic cell (DC)-enriched population of testicular draining lymph node (LN) cells before (A) and after (B) Ox-62-coupled magnetic beads separation. Filled histograms represent all viable cells in the LN single cell suspension labelled with fluorescent conju- gated antibodies directed against CD11c (DC), major histocompatibility complex II, CD45 RA (B cells) or CD3 (T cells). The thick black lines indicate the respective isotype controls. All data are representative of at least three independent experiments with similar results.

    Article Snippet: Subsequently, enriched DC populations were stained with the primary mouse anti-rat-CD11c-Alexa Fluor 647 antibody (AbD Serotec, Oxford, UK) followed by incubation with mouse anti-rat CD3, MHC II and CD45 RA (B-cell marker) antibody (BD Biosciences, Heidelberg, Germany) and analysed by flow cytometry (Table 1).

    Techniques: Magnetic Beads, Suspension, Immunopeptidomics