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α6 nachr subunit antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs 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.
    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/anc-006/pmc06954311-41-7-4?v=Alomone+Labs
    Average 90 stars, based on 1 article reviews
    α6 nachr subunit antibody - by Bioz Stars, 2026-07
    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

    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: Western Blot, Expressing, Blocking Assay



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    Alomone Labs 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.
    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/anc-006/pmc06954311-41-7-4?v=Alomone+Labs
    Average 90 stars, based on 1 article reviews
    α6 nachr subunit antibody - by Bioz Stars, 2026-07
    90/100 stars
      Buy from Supplier

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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
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    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: Although, a control antigen (Alomone) blocks the α6 nAChR subunit antibody from binding in the PC12 pheochromocytoma cells, a more standard form of validation is necessary ( Uhlen et al. 2016 ).

    Techniques: Western Blot, Expressing, Blocking Assay

    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: Although, a control antigen (Alomone) blocks the α6 nAChR subunit antibody from binding in the PC12 pheochromocytoma cells, a more standard form of validation is necessary ( Uhlen et al. 2016 ).

    Techniques: Western Blot, Expressing, Blocking Assay

    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

    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: Western Blot, Expressing, Blocking Assay