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grid2 extracellular antibody  (Alomone Labs)


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    Structured Review

    Alomone Labs grid2 extracellular antibody
    A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, <t>Grid2.</t> Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.
    Grid2 Extracellular Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/agc-039/bio_rxiv__2025__11__09__687499-38-13-18?v=Alomone+Labs
    Average 93 stars, based on 1 article reviews
    grid2 extracellular antibody - by Bioz Stars, 2026-07
    93/100 stars

    Images

    1) Product Images from "Anti-Kv1.2 Immunoprecipitation Identifies shared mGluR1-Associated Signalosome Complex proteins and PKC-Mediated Regulation of Kv1.2 in the Cerebellum"

    Article Title: Anti-Kv1.2 Immunoprecipitation Identifies shared mGluR1-Associated Signalosome Complex proteins and PKC-Mediated Regulation of Kv1.2 in the Cerebellum

    Journal: bioRxiv

    doi: 10.1101/2025.11.09.687499

    A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, Grid2. Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.
    Figure Legend Snippet: A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, Grid2. Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.

    Techniques Used: Western Blot, Mass Spectrometry, Control, Comparison, Biomarker Discovery, Co-Immunoprecipitation Assay, Immunoprecipitation



    Similar Products

    grid2 extracellular antibody  (Alomone Labs)
    93
    Alomone Labs grid2 extracellular antibody
    A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, <t>Grid2.</t> Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.
    Grid2 Extracellular Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/agc-039/bio_rxiv__2025__11__09__687499-38-13-18?v=Alomone+Labs
    Average 93 stars, based on 1 article reviews
    grid2 extracellular antibody - by Bioz Stars, 2026-07
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, Grid2. Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.

    Journal: bioRxiv

    Article Title: Anti-Kv1.2 Immunoprecipitation Identifies shared mGluR1-Associated Signalosome Complex proteins and PKC-Mediated Regulation of Kv1.2 in the Cerebellum

    doi: 10.1101/2025.11.09.687499

    Figure Lengend Snippet: A) Western blot of Kv1.2 IP aliquot saved from the TMT mass spectrometry experiment; cerebellar slices treated with DHPG for 10 min or 60 min. The IP was probed for PKC gamma and Kv1.2 (above). The bar graph below shows quantification of PKC gamma relative to Kv1.2. N=2 experiments ** indicates significant difference compared to control. P<0.01 with a one-way ANOVA multiple comparison test. B&C) Independent validation of the Co-ip proteins identified in the MS experiment. Cerebellar lysates were subjected to Kv1.2 immunoprecipitation and were analyzed via western blots with antibodies against CaMKII (PAN-CaMKII antibody), Gq/G11 subunit, PKC-γ, Grid2. Pre – indicates the input, Igg – control Mouse antibody, Post – lysate after immunoprecipitation, IP – immunoprecipitation with anti-Kv1.2 Antibody.

    Article Snippet: PKC - γ and p-PKC - γ thr514 antibodies were purchased from Genetex, Grid2 extracellular Antibody was from Alomone labs. Anti – mouse Dx700 was purchased from Invitrogen and anti – rabbit 800 infrared dye conjugated 2° antibodies were purchased from Rockland INC.

    Techniques: Western Blot, Mass Spectrometry, Control, Comparison, Biomarker Discovery, Co-Immunoprecipitation Assay, Immunoprecipitation