rabbit anti sk1  (Alomone Labs)


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    Structured Review

    Alomone Labs rabbit anti sk1
    MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of <t>SK1,</t> SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p
    Rabbit Anti Sk1, 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/result/rabbit anti sk1/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti sk1 - by Bioz Stars, 2022-05
    93/100 stars

    Images

    1) Product Images from "Alterations of Electrophysiological Properties and Ion Channel Expression in Prefrontal Cortex of a Mouse Model of Schizophrenia"

    Article Title: Alterations of Electrophysiological Properties and Ion Channel Expression in Prefrontal Cortex of a Mouse Model of Schizophrenia

    Journal: Frontiers in Cellular Neuroscience

    doi: 10.3389/fncel.2019.00554

    MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of SK1, SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p
    Figure Legend Snippet: MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of SK1, SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p

    Techniques Used: Expressing, Western Blot

    2) Product Images from "Role of the endothelial caveolae microdomain in shear stress–mediated coronary vasorelaxation"

    Article Title: Role of the endothelial caveolae microdomain in shear stress–mediated coronary vasorelaxation

    Journal: The Journal of Biological Chemistry

    doi: 10.1074/jbc.M117.786152

    Subcellular distribution of SK, IK, and TRP channels in freshly isolated nonpassaged BCECs is shown. A , the subcellular distribution of SK1, SK2, SK3, IK, TRPC4, and TRPV4 in freshly isolated BCECs was measured by density gradient fractionation, with fraction 1 being the lightest and fraction 12 the heaviest. Western blots against anti-SK1, anti-SK2, anti-SK3, anti-IK, anti-TRPV4, anti-TRPC4, and anti-Cav-1 antibodies show that SK1, SK3, and TRPV4 are detected in the low-buoyant density, caveolae-rich fractions, whereas SK2, IK, and TRPC4 are mainly found in the high-density non-lipid raft fractions and absent in the caveolae-rich fractions. B , immunoprecipitates of anti-Cav-1 antibody after incubation with the low-buoyant density fraction 5 were blotted against anti-SK1, anti-SK3, anti-IK, and anti-TRPV4 antibodies. Pulldowns using nonimmune IgG served as controls. C, immunoprecipitates of anti-TRPV4 or anti-SK3 antibodies from the low-buoyant density fraction 5 were blotted against anti-Cav-1 antibodies. Pulldown using nonimmune IgG served as controls. D, BCEC in situ proximity ligation assay (PLA). The fluorescent signal generated by labeled complementary oligonucleotide probes after a 100-min amplification reaction at 37 °C in BCECs treated with mouse anti-Cav-1 and rabbit anti-SK3 or rabbit anti-TRPV4 antibodies. The nuclei were counterstained with DAPI, and the PLA signals were visualized at 40× magnification under a Zeiss 510 Meta Confocal Laser Scanning Microscope equipped with DAPI/Texas Red filters and analyzed using Zeiss 510 software.
    Figure Legend Snippet: Subcellular distribution of SK, IK, and TRP channels in freshly isolated nonpassaged BCECs is shown. A , the subcellular distribution of SK1, SK2, SK3, IK, TRPC4, and TRPV4 in freshly isolated BCECs was measured by density gradient fractionation, with fraction 1 being the lightest and fraction 12 the heaviest. Western blots against anti-SK1, anti-SK2, anti-SK3, anti-IK, anti-TRPV4, anti-TRPC4, and anti-Cav-1 antibodies show that SK1, SK3, and TRPV4 are detected in the low-buoyant density, caveolae-rich fractions, whereas SK2, IK, and TRPC4 are mainly found in the high-density non-lipid raft fractions and absent in the caveolae-rich fractions. B , immunoprecipitates of anti-Cav-1 antibody after incubation with the low-buoyant density fraction 5 were blotted against anti-SK1, anti-SK3, anti-IK, and anti-TRPV4 antibodies. Pulldowns using nonimmune IgG served as controls. C, immunoprecipitates of anti-TRPV4 or anti-SK3 antibodies from the low-buoyant density fraction 5 were blotted against anti-Cav-1 antibodies. Pulldown using nonimmune IgG served as controls. D, BCEC in situ proximity ligation assay (PLA). The fluorescent signal generated by labeled complementary oligonucleotide probes after a 100-min amplification reaction at 37 °C in BCECs treated with mouse anti-Cav-1 and rabbit anti-SK3 or rabbit anti-TRPV4 antibodies. The nuclei were counterstained with DAPI, and the PLA signals were visualized at 40× magnification under a Zeiss 510 Meta Confocal Laser Scanning Microscope equipped with DAPI/Texas Red filters and analyzed using Zeiss 510 software.

    Techniques Used: Isolation, Fractionation, Western Blot, Incubation, In Situ, Proximity Ligation Assay, Generated, Labeling, Amplification, Laser-Scanning Microscopy, Software

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    Alomone Labs rabbit anti sk1
    MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of <t>SK1,</t> SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p
    Rabbit Anti Sk1, 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/result/rabbit anti sk1/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti sk1 - by Bioz Stars, 2022-05
    93/100 stars
      Buy from Supplier

    Image Search Results


    MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of SK1, SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p

    Journal: Frontiers in Cellular Neuroscience

    Article Title: Alterations of Electrophysiological Properties and Ion Channel Expression in Prefrontal Cortex of a Mouse Model of Schizophrenia

    doi: 10.3389/fncel.2019.00554

    Figure Lengend Snippet: MIA-SI increases the expression levels of Nav1.2 and SK3 channels. (A) Representative immunoblots of Nav1.2, Nav1.6 and tubulin, run on a same gel. Each band represents samples from one animal. (B,C) Average Nav1.2 and Nav1.6 protein levels in PFC in two experimental groups. (D) Averaged ratio of Nav1.2 to the sum of Nav1.2 and Nav1.6 was increased by MIA-SI. (E) Representative immunoblots of SK1, SK2, SK3, and tubulin run on a same gel. (F–H) Average SK1, SK2, and SK3 protein levels in PFC of experimental animals. For each protein, blots were cropped to retain the important bands at the same size of the same membrane. ∗ p

    Article Snippet: The primary antibodies are as follows: mouse anti-Nav1.2, clone K69/3, 1:200 (Neuromab, Davis, CA, United States); rabbit anti-Nav1.6, 1:200; rabbit anti-SK1, #APC-039, 1:200; rabbit anti-SK2, #APC-028, 1:200; rabbit anti-SK3 N-term, #APC-025, 1:200 (Alomone Labs, Jerusalem, Israel); mouse anti-α-tubulin, clone DM1A, 1:1000 (Sigma-Aldrich, St. Louis, MO, United States).

    Techniques: Expressing, Western Blot

    Subcellular distribution of SK, IK, and TRP channels in freshly isolated nonpassaged BCECs is shown. A , the subcellular distribution of SK1, SK2, SK3, IK, TRPC4, and TRPV4 in freshly isolated BCECs was measured by density gradient fractionation, with fraction 1 being the lightest and fraction 12 the heaviest. Western blots against anti-SK1, anti-SK2, anti-SK3, anti-IK, anti-TRPV4, anti-TRPC4, and anti-Cav-1 antibodies show that SK1, SK3, and TRPV4 are detected in the low-buoyant density, caveolae-rich fractions, whereas SK2, IK, and TRPC4 are mainly found in the high-density non-lipid raft fractions and absent in the caveolae-rich fractions. B , immunoprecipitates of anti-Cav-1 antibody after incubation with the low-buoyant density fraction 5 were blotted against anti-SK1, anti-SK3, anti-IK, and anti-TRPV4 antibodies. Pulldowns using nonimmune IgG served as controls. C, immunoprecipitates of anti-TRPV4 or anti-SK3 antibodies from the low-buoyant density fraction 5 were blotted against anti-Cav-1 antibodies. Pulldown using nonimmune IgG served as controls. D, BCEC in situ proximity ligation assay (PLA). The fluorescent signal generated by labeled complementary oligonucleotide probes after a 100-min amplification reaction at 37 °C in BCECs treated with mouse anti-Cav-1 and rabbit anti-SK3 or rabbit anti-TRPV4 antibodies. The nuclei were counterstained with DAPI, and the PLA signals were visualized at 40× magnification under a Zeiss 510 Meta Confocal Laser Scanning Microscope equipped with DAPI/Texas Red filters and analyzed using Zeiss 510 software.

    Journal: The Journal of Biological Chemistry

    Article Title: Role of the endothelial caveolae microdomain in shear stress–mediated coronary vasorelaxation

    doi: 10.1074/jbc.M117.786152

    Figure Lengend Snippet: Subcellular distribution of SK, IK, and TRP channels in freshly isolated nonpassaged BCECs is shown. A , the subcellular distribution of SK1, SK2, SK3, IK, TRPC4, and TRPV4 in freshly isolated BCECs was measured by density gradient fractionation, with fraction 1 being the lightest and fraction 12 the heaviest. Western blots against anti-SK1, anti-SK2, anti-SK3, anti-IK, anti-TRPV4, anti-TRPC4, and anti-Cav-1 antibodies show that SK1, SK3, and TRPV4 are detected in the low-buoyant density, caveolae-rich fractions, whereas SK2, IK, and TRPC4 are mainly found in the high-density non-lipid raft fractions and absent in the caveolae-rich fractions. B , immunoprecipitates of anti-Cav-1 antibody after incubation with the low-buoyant density fraction 5 were blotted against anti-SK1, anti-SK3, anti-IK, and anti-TRPV4 antibodies. Pulldowns using nonimmune IgG served as controls. C, immunoprecipitates of anti-TRPV4 or anti-SK3 antibodies from the low-buoyant density fraction 5 were blotted against anti-Cav-1 antibodies. Pulldown using nonimmune IgG served as controls. D, BCEC in situ proximity ligation assay (PLA). The fluorescent signal generated by labeled complementary oligonucleotide probes after a 100-min amplification reaction at 37 °C in BCECs treated with mouse anti-Cav-1 and rabbit anti-SK3 or rabbit anti-TRPV4 antibodies. The nuclei were counterstained with DAPI, and the PLA signals were visualized at 40× magnification under a Zeiss 510 Meta Confocal Laser Scanning Microscope equipped with DAPI/Texas Red filters and analyzed using Zeiss 510 software.

    Article Snippet: For immunoblotting, the proteins were boiled with 15 μl SDS-PAGE loading buffer at 100 °C, resolved by polyacrylamide gel electrophoresis, transferred to nitrocellulose membrane, and then blotted against rabbit anti-Cav-1, rabbit anti-SK1 (1:200, Alomone Labs, APC-039), rabbit anti-SK2 (1:200, Alomone Labs, APC-028), rabbit anti-SK3 (1:200, Alomone Labs, APC-025), anti-TRPC4 (1:200, Alomone Labs, ACC-018), rabbit anti-TRPV4 (1:200, Alomone Labs, ACC-034), and anti-TRPC4 (Alomone Labs, ACC-018) antibodies.

    Techniques: Isolation, Fractionation, Western Blot, Incubation, In Situ, Proximity Ligation Assay, Generated, Labeling, Amplification, Laser-Scanning Microscopy, Software