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polyclonal α6 nachr subunit antibody  (Alomone Labs)


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    Alomone Labs polyclonal α6 nachr subunit antibody
    Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of <t>α6</t> <t>nAChR</t> subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.
    Polyclonal α6 Nachr Subunit Antibody, supplied by Alomone Labs, 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/polyclonal+%CE%B16+nachr+subunit+antibody/Anti-Nicotinic+Acetylcholine+Receptor+%CE%B16+(CHRNA6)+(extracellular)+Antibody/pmc06954311-38-15-21
    Average 90 stars, based on 1 article reviews
    polyclonal α6 nachr subunit antibody - by Bioz Stars, 2026-09
    90/100 stars

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    1) Product Images from "Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody"

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody

    Journal: Psychopharmacology

    doi: 10.1007/s00213-019-05413-x

    Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of α6 nAChR subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.
    Figure Legend Snippet: Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of α6 nAChR subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.

    Techniques Used: Western Blot, Expressing, Blocking Assay, Control

    Genetic validation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A.) Western blot and B.) relative band intensity quantification of α6 nAChR subunit expression and antigen block from whole brain tissue collected from male and female WT and α6 KO C57BL/6J mice, n=4 animals/genotype; **p< 0.01 and ***p< 0.001 α6 antibody vs. α6 antibody + antigen normalized signal. GAPDH is used as a loading control.
    Figure Legend Snippet: Genetic validation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A.) Western blot and B.) relative band intensity quantification of α6 nAChR subunit expression and antigen block from whole brain tissue collected from male and female WT and α6 KO C57BL/6J mice, n=4 animals/genotype; **p< 0.01 and ***p< 0.001 α6 antibody vs. α6 antibody + antigen normalized signal. GAPDH is used as a loading control.

    Techniques Used: Biomarker Discovery, Western Blot, Expressing, Blocking Assay, Control

    Related Articles

    Western Blot:

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody
    Article Snippet: Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).. Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).. In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.

    Expressing:

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody
    Article Snippet: Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).. Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).. In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.

    Blocking Assay:

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody
    Article Snippet: Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).. Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).. In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.

    Control:

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody
    Article Snippet: Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).. Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).. In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.

    Biomarker Discovery:

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody
    Article Snippet: Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).Data highlights that the immunoreactivity for the antibody binding of these nAChR subunits is equivalent in wild-type and nAChR subunit knock-out (KO) animals ( Moser et al. 2007 ).. Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).. In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.In order to detect whether we can quantify α6 nAChR subunit protein expression in wild type (WT) Sprague Dawley rats and C57BL/6J mice we used quantitative western blot.



    Similar Products

    polyclonal α6 nachr subunit antibody  (Alomone Labs)
    90
    Alomone Labs polyclonal α6 nachr subunit antibody
    Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of <t>α6</t> <t>nAChR</t> subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.
    Polyclonal α6 Nachr Subunit Antibody, supplied by Alomone Labs, 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/polyclonal+%CE%B16+nachr+subunit+antibody/Anti-Nicotinic+Acetylcholine+Receptor+%CE%B16+(CHRNA6)+(extracellular)+Antibody/pmc06954311-38-15-21
    Average 90 stars, based on 1 article reviews
    polyclonal α6 nachr subunit antibody - by Bioz Stars, 2026-09
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of α6 nAChR subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.

    Journal: Psychopharmacology

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody

    doi: 10.1007/s00213-019-05413-x

    Figure Lengend Snippet: Evaluation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A western blot of α6 nAChR subunit expression and antigen block in bilateral ventral tegmental tissue punches collected from male Sprague Dawley rats. n=2 animals total. GAPDH is used as a loading control.

    Article Snippet: Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).

    Techniques: Western Blot, Expressing, Blocking Assay, Control

    Genetic validation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A.) Western blot and B.) relative band intensity quantification of α6 nAChR subunit expression and antigen block from whole brain tissue collected from male and female WT and α6 KO C57BL/6J mice, n=4 animals/genotype; **p< 0.01 and ***p< 0.001 α6 antibody vs. α6 antibody + antigen normalized signal. GAPDH is used as a loading control.

    Journal: Psychopharmacology

    Article Title: Specificity of a rodent alpha(α)6 nicotinic acetylcholine receptor subunit antibody

    doi: 10.1007/s00213-019-05413-x

    Figure Lengend Snippet: Genetic validation of an alpha(α)6 nicotinic acetylcholine receptor subunit antibody. A.) Western blot and B.) relative band intensity quantification of α6 nAChR subunit expression and antigen block from whole brain tissue collected from male and female WT and α6 KO C57BL/6J mice, n=4 animals/genotype; **p< 0.01 and ***p< 0.001 α6 antibody vs. α6 antibody + antigen normalized signal. GAPDH is used as a loading control.

    Article Snippet: Thus, the purpose of this study is to validate the specificity of the commercially available polyclonal α6 nAChR subunit antibody from Alomone Labs (cat. #: ANC-006, Jerusalem, Israel).

    Techniques: Biomarker Discovery, Western Blot, Expressing, Blocking Assay, Control