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adapter molecule 1 iba1 primary antibody  (Proteintech)


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    Proteintech adapter molecule 1 iba1 primary antibody
    Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with <t>IBA1</t> (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.
    Adapter Molecule 1 Iba1 Primary Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 288 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/adapter molecule 1 iba1 primary antibody/product/Proteintech
    Average 96 stars, based on 288 article reviews
    adapter molecule 1 iba1 primary antibody - by Bioz Stars, 2026-05
    96/100 stars

    Images

    1) Product Images from "Naltrexone treatment improves anxiety- and depression-like behavior in alcohol-exposed mice"

    Article Title: Naltrexone treatment improves anxiety- and depression-like behavior in alcohol-exposed mice

    Journal: Behavioural Pharmacology

    doi: 10.1097/FBP.0000000000000876

    Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with IBA1 (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.
    Figure Legend Snippet: Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with IBA1 (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.

    Techniques Used: Activation Assay, Immunofluorescence, Labeling, Derivative Assay



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    Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with <t>IBA1</t> (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.
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    Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with <t>IBA1</t> (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.
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    Image Search Results


    Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with IBA1 (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.

    Journal: Behavioural Pharmacology

    Article Title: Naltrexone treatment improves anxiety- and depression-like behavior in alcohol-exposed mice

    doi: 10.1097/FBP.0000000000000876

    Figure Lengend Snippet: Naltrexone treatment ameliorates microglial activation in alcohol-exposed mice. (a) Immunofluorescence images of microglia labeled with IBA1 (green) in the BLA region (DAPI, blue, for nuclear counterstaining); each image is a representative result from n = 4 independent mice, with images in each treatment group derived from brain tissues of different mice and corresponding coronal sections of the same brain region to ensure intergroup comparability ( n = 4 each group). (b) Quantification of microglial cell numbers in the BLA region ( F = 10.53, DF = 11, P < 0.01; n = 4 each group) * P < 0.05, ** P < 0.01, *** P < 0.001. BLA, basolateral amygdala; DAPI, 4',6-diamidino-2-phenylindole.

    Article Snippet: Sections were blocked (5% BSA + 0.5% Triton X-100 in PBS, 1 h, room temperature) and incubated with anti-ionized calcium-binding adapter molecule 1 (IBA1) primary antibody (1 : 500, Proteintech, China, 4°C overnight), followed by Alexa Fluor 488-conjugated secondary antibody (Thermo Fisher Scientific, Waltham, USA, 1 h, room temperature).

    Techniques: Activation Assay, Immunofluorescence, Labeling, Derivative Assay