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chicken polyclonal map2 antisera  (EnCor Biotechnology)

 
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    EnCor Biotechnology chicken polyclonal map2 antisera
    Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated <t>MAP2</t> staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.
    Chicken Polyclonal Map2 Antisera, supplied by EnCor Biotechnology, 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/chicken+polyclonal+map2+antisera/pmc09139467-326-24-28?v=EnCor+Biotechnology
    Average 90 stars, based on 1 article reviews
    chicken polyclonal map2 antisera - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Effects of 9-t-butyl doxycycline on the innate immune response to CNS ischemia-reperfusion injury"

    Article Title: Effects of 9-t-butyl doxycycline on the innate immune response to CNS ischemia-reperfusion injury

    Journal: Experimental and molecular pathology

    doi: 10.1016/j.yexmp.2020.104601

    Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated MAP2 staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.
    Figure Legend Snippet: Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated MAP2 staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.

    Techniques Used: Staining, Immunohistochemistry



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    chicken polyclonal map2 antisera  (EnCor Biotechnology)
    90
    EnCor Biotechnology chicken polyclonal map2 antisera
    Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated <t>MAP2</t> staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.
    Chicken Polyclonal Map2 Antisera, supplied by EnCor Biotechnology, 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/chicken+polyclonal+map2+antisera/pmc09139467-326-24-28?v=EnCor+Biotechnology
    Average 90 stars, based on 1 article reviews
    chicken polyclonal map2 antisera - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated MAP2 staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.

    Journal: Experimental and molecular pathology

    Article Title: Effects of 9-t-butyl doxycycline on the innate immune response to CNS ischemia-reperfusion injury

    doi: 10.1016/j.yexmp.2020.104601

    Figure Lengend Snippet: Effect of 9-TB on cortical immune infiltration and neuronal injury after CNS ischemia-reperfusion. (A) 9-TB limits cortical injury in 3VO/LPS exposed mice, measured by areas of attenuated MAP2 staining. ****p < 0.0001, SHAM/SAL/VEH (n=5) vs. 3VO/LPS/VEH (n=6); ##p < 0.01, 3VO/LPS/VEH vs. 3VO/LPS/9-TB (n=7); SHAM/SAL/9-TB (n=6). (B-C) Effects of 3VO/LPS and 9-TB on the accumulation of EGFP(+) myeloid cells within the cerebral cortex of LysM-EGFP mice three days following ischemia-reperfusion. ***p < 0.001 SHAM/SAL vs. 3VO/LPS. Scale bar = 200 μm. (D) Association between cortical myeloid cell accumulation and MAP2(+) loss. Fine, curved lines around slope represent 95% confidence interval. Y = 145X - 957. (E) IHC staining of cortical sections for MAP2 depicting the relationship between EGFP(+) granulocyte accumulation with injured (left, MAP2Low outlined in white) or uninjured (right, MAP2High) parenchyma. Scale bar = 200 μm. Data are expressed as the mean ± S.D. (n = 5–7 mice/group). Statistical comparisons were made by 2-way ANOVA.

    Article Snippet: Floating brain sections were washed with PBS and blocked in 10% goat serum for 1 hour at 20°C prior to immunohistochemical (IHC) staining with chicken polyclonal MAP2 antisera (EnCor, Gainesville, FL; 1:1000) incubated overnight at 4 °C followed by an Alexa Fluor TM 647 secondary antibody (Invitrogen, Carlsbad, CA; 1:500) for 1 hour at room temperature.

    Techniques: Staining, Immunohistochemistry