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rat-anti-mouse mac2 primary antibody  (Cedarlane)


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    Cedarlane rat-anti-mouse mac2 primary antibody
    Rat Anti Mouse Mac2 Primary Antibody, supplied by Cedarlane, 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/rat+anti-mouse+mac2+primary/anti+mac+2/pmc10723050__pnas__2314698120__sapp-110-9-13
    Average 90 stars, based on 1 article reviews
    rat-anti-mouse mac2 primary antibody - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Supporting Information for Distinct mouse models of Stargardt disease display differences in inflammatory responses and pharmacological targeting of ceramides
    Article Snippet: Sections were dried and dehydrated with ethanol, before blocking for 1 hr followed 1 hr incubation with rat anti-mouse Mac2 primary at a 1:1000 dilution in blocking buffer (CedarLane Labs, Burlington NC, #CL8942AP).

    Incubation:

    Article Title: Supporting Information for Distinct mouse models of Stargardt disease display differences in inflammatory responses and pharmacological targeting of ceramides
    Article Snippet: Sections were dried and dehydrated with ethanol, before blocking for 1 hr followed 1 hr incubation with rat anti-mouse Mac2 primary at a 1:1000 dilution in blocking buffer (CedarLane Labs, Burlington NC, #CL8942AP).



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    ACKR2 controls the accumulation of macrophages in the mammary gland. (A) Flow cytometry was used to identify the percentage of CD11b + F4/80 + macrophages within the CD45 + population of the mammary gland during development. Gating based on fluorescence minus one (FMO) controls is shown. (B) FACS analysis of wild-type and Ackr2 −/− -deficient glands was carried out at 6, 6.5, 8 and 12 weeks. Results were combined from two independent experiments, n =8-11. (C) <t>Mac2+</t> cells, indicated by arrowheads, were visualised within the developing mammary gland by immunohistochemistry. Representative 40× bright-field images of Mac2-stained sections from wild-type and Ackr2 −/− glands are shown. (D,E) The number of Mac2+ cells per gland was the average counted from five individual FOV (40×) either (D) around TEBs or (E) from within adipose tissue, from 6 week ( n =3), 6.5 week ( n =5) and 8 week (wild type n =5, KO n =4) glands. Significantly different results are indicated. Error bars represent s.e.m.
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    ACKR2 controls the accumulation of macrophages in the mammary gland. (A) Flow cytometry was used to identify the percentage of CD11b + F4/80 + macrophages within the CD45 + population of the mammary gland during development. Gating based on fluorescence minus one (FMO) controls is shown. (B) FACS analysis of wild-type and Ackr2 −/− -deficient glands was carried out at 6, 6.5, 8 and 12 weeks. Results were combined from two independent experiments, n =8-11. (C) <t>Mac2+</t> cells, indicated by arrowheads, were visualised within the developing mammary gland by immunohistochemistry. Representative 40× bright-field images of Mac2-stained sections from wild-type and Ackr2 −/− glands are shown. (D,E) The number of Mac2+ cells per gland was the average counted from five individual FOV (40×) either (D) around TEBs or (E) from within adipose tissue, from 6 week ( n =3), 6.5 week ( n =5) and 8 week (wild type n =5, KO n =4) glands. Significantly different results are indicated. Error bars represent s.e.m.
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    Image Search Results


    ACKR2 controls the accumulation of macrophages in the mammary gland. (A) Flow cytometry was used to identify the percentage of CD11b + F4/80 + macrophages within the CD45 + population of the mammary gland during development. Gating based on fluorescence minus one (FMO) controls is shown. (B) FACS analysis of wild-type and Ackr2 −/− -deficient glands was carried out at 6, 6.5, 8 and 12 weeks. Results were combined from two independent experiments, n =8-11. (C) Mac2+ cells, indicated by arrowheads, were visualised within the developing mammary gland by immunohistochemistry. Representative 40× bright-field images of Mac2-stained sections from wild-type and Ackr2 −/− glands are shown. (D,E) The number of Mac2+ cells per gland was the average counted from five individual FOV (40×) either (D) around TEBs or (E) from within adipose tissue, from 6 week ( n =3), 6.5 week ( n =5) and 8 week (wild type n =5, KO n =4) glands. Significantly different results are indicated. Error bars represent s.e.m.

    Journal: Development (Cambridge, England)

    Article Title: Atypical chemokine receptor ACKR2 controls branching morphogenesis in the developing mammary gland

    doi: 10.1242/dev.139733

    Figure Lengend Snippet: ACKR2 controls the accumulation of macrophages in the mammary gland. (A) Flow cytometry was used to identify the percentage of CD11b + F4/80 + macrophages within the CD45 + population of the mammary gland during development. Gating based on fluorescence minus one (FMO) controls is shown. (B) FACS analysis of wild-type and Ackr2 −/− -deficient glands was carried out at 6, 6.5, 8 and 12 weeks. Results were combined from two independent experiments, n =8-11. (C) Mac2+ cells, indicated by arrowheads, were visualised within the developing mammary gland by immunohistochemistry. Representative 40× bright-field images of Mac2-stained sections from wild-type and Ackr2 −/− glands are shown. (D,E) The number of Mac2+ cells per gland was the average counted from five individual FOV (40×) either (D) around TEBs or (E) from within adipose tissue, from 6 week ( n =3), 6.5 week ( n =5) and 8 week (wild type n =5, KO n =4) glands. Significantly different results are indicated. Error bars represent s.e.m.

    Article Snippet: Slides were blocked using a 20% goat serum (Vector Labs) before staining overnight at 4°C with a 1 in 6000 dilution in PBS containing 1% BSA (Sigma) of either primary rat anti-mouse Mac2 antibody (Cedarlane) or the isotype control antibody IgG2a (BD Biosciences).

    Techniques: Flow Cytometry, Fluorescence, Immunohistochemistry, Staining