anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Two bar diagrams on the left show the relative protein expression of Kv4.3 and <t>KChiP2</t> subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Anti Kchip2, 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
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    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    93/100 stars

    Images

    1) Product Images from "Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise"

    Article Title: Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise

    Journal: bioRxiv

    doi: 10.1101/2022.07.13.499876

    Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Figure Legend Snippet: Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.

    Techniques Used: Expressing, Western Blot

    kchip2  (Alomone Labs)


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    Alomone Labs kchip2
    Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Anti Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Anti Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    kchip2 mab neuromabs  (Alomone Labs)


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    Alomone Labs kchip2 mab neuromabs
    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). <t>KChIP2</t> is a cytosolic protein, and thus is not glycosylated.
    Kchip2 Mab Neuromabs, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Long-Term Fish Oil Supplementation Induces Cardiac Electrical Remodeling by Changing Channel Protein Expression in the Rabbit Model"

    Article Title: Long-Term Fish Oil Supplementation Induces Cardiac Electrical Remodeling by Changing Channel Protein Expression in the Rabbit Model

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0010140

    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). KChIP2 is a cytosolic protein, and thus is not glycosylated.
    Figure Legend Snippet: ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). KChIP2 is a cytosolic protein, and thus is not glycosylated.

    Techniques Used: Western Blot

    ( A ) Immunoblot images of Kv4.2, Kv4.3, and KChIP2 (∼80 ug/lane). ( B ) Immunoblot images of Kv1.4 (∼160 ug/lane). Size marker bands (in kDa) are listed on the left. Sizes for proteins of interest are marked on the right. Note that for panel (A) here and , each channel subunit immunoblot was corrected by its own α-actin immunoblot for loading variations, although only one representative α-actin immunoblot is shown. Loading variation in Fig. 6B was further checked by coomassie blue (CB) stain. ( C ) Data summary: background-subtracted band intensities were divided by corresponding α-actin band intensity, and then normalized by the mean value of control lanes.
    Figure Legend Snippet: ( A ) Immunoblot images of Kv4.2, Kv4.3, and KChIP2 (∼80 ug/lane). ( B ) Immunoblot images of Kv1.4 (∼160 ug/lane). Size marker bands (in kDa) are listed on the left. Sizes for proteins of interest are marked on the right. Note that for panel (A) here and , each channel subunit immunoblot was corrected by its own α-actin immunoblot for loading variations, although only one representative α-actin immunoblot is shown. Loading variation in Fig. 6B was further checked by coomassie blue (CB) stain. ( C ) Data summary: background-subtracted band intensities were divided by corresponding α-actin band intensity, and then normalized by the mean value of control lanes.

    Techniques Used: Western Blot, Marker, Staining

    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Two bar diagrams on the left show the relative protein expression of Kv4.3 and <t>KChiP2</t> subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Anti Kchip2, 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/anti kchip2/product/Alomone Labs
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    Images

    1) Product Images from "Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise"

    Article Title: Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise

    Journal: bioRxiv

    doi: 10.1101/2022.07.13.499876

    Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Figure Legend Snippet: Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.

    Techniques Used: Expressing, Western Blot

    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Two bar diagrams on the left show the relative protein expression of Kv4.3 and <t>KChiP2</t> subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Anti Kchip2, 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/anti kchip2/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
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    anti kchip2 - by Bioz Stars, 2024-05
    93/100 stars

    Images

    1) Product Images from "Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise"

    Article Title: Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise

    Journal: bioRxiv

    doi: 10.1101/2022.07.13.499876

    Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Figure Legend Snippet: Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.

    Techniques Used: Expressing, Western Blot

    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Anti Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    kchip2 apc 142  (Alomone Labs)


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    Alomone Labs kchip2 apc 142
    Kchip2 Apc 142, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti kchip2 antibody  (Alomone Labs)


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    Alomone Labs anti kchip2 antibody
    Anti Kchip2 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti kchip2 antibody/product/Alomone Labs
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    anti kchip2  (Alomone Labs)


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    Alomone Labs anti kchip2
    Anti Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti kchip2/product/Alomone Labs
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    Alomone Labs anti kchip2
    Two bar diagrams on the left show the relative protein expression of Kv4.3 and <t>KChiP2</t> subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Anti Kchip2, 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/anti kchip2/product/Alomone Labs
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti kchip2 - by Bioz Stars, 2024-05
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    Alomone Labs kchip2
    Two bar diagrams on the left show the relative protein expression of Kv4.3 and <t>KChiP2</t> subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.
    Kchip2, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kchip2/product/Alomone Labs
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kchip2 - by Bioz Stars, 2024-05
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    86
    Alomone Labs kchip2 mab neuromabs
    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). <t>KChIP2</t> is a cytosolic protein, and thus is not glycosylated.
    Kchip2 Mab Neuromabs, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs kchip2 apc 142
    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). <t>KChIP2</t> is a cytosolic protein, and thus is not glycosylated.
    Kchip2 Apc 142, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Alomone Labs anti kchip2 antibody
    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). <t>KChIP2</t> is a cytosolic protein, and thus is not glycosylated.
    Anti Kchip2 Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti kchip2 antibody/product/Alomone Labs
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    Image Search Results


    Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.

    Journal: bioRxiv

    Article Title: Cardiac electrophysiological remodeling associated with enhanced arrhythmia susceptibilty in a canine model of elite exercise

    doi: 10.1101/2022.07.13.499876

    Figure Lengend Snippet: Two bar diagrams on the left show the relative protein expression of Kv4.3 and KChiP2 subunits determined by Western blot in sedentary (n=12 dogs) and trained dog (n=12) left ventricular samples. Bottom panels indicates the representative Kv4.3 and KChIP2 bands and their corresponding loading control (GAPDH). Two bar diagrams on the right panels show the relative density of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling obtained from the sedentary (n=30 cells/6 dogs) and trained (n=30 cells/6 dogs) groups. Bottom panels on the right show original immunofluorescent images of dog cardiomyocytes with Kv4.3 and KChiP2 immunolabelling. Figure 6–Source Data 1 Protein expression of Kv4.3 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 2 Protein expression of KChiP2 subunit determined by Western blot technique in sedentary and trained dogs. Figure 6–Source Data 3 Relative density of Kv4.3 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 4 Relative density of KChiP2 subunit determined by immunocytochemical technique in sedentary and trained dogs. Figure 6–Source Data 5 Original, unedited membranes of western blots with the relevant bands clearly labelled. Figure 6–Source Data 6 Original files of the full raw unedited membranes of western blots.

    Article Snippet: The membrane was blocked with 2.5% non-fat milk for 1 hour at room temperature and immunolabelled overnight at 4°C with anti-KChIP2 (Alomone, #APC-142, RRID:AB_2756744) and anti-Kv4.3 (Alomone, #APC-017, RRID:AB_2040178) primary antibody diluted to 1:1000.

    Techniques: Expressing, Western Blot

    ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). KChIP2 is a cytosolic protein, and thus is not glycosylated.

    Journal: PLoS ONE

    Article Title: Long-Term Fish Oil Supplementation Induces Cardiac Electrical Remodeling by Changing Channel Protein Expression in the Rabbit Model

    doi: 10.1371/journal.pone.0010140

    Figure Lengend Snippet: ( A ) – ( D ) Immunoblot images of rabbit and rat hearts (except (A), right lane, rat brain), probed with Abs marked on top. Kv1.4 was detected in whole tissue lysates (WTL), while the other three proteins were detected in membrane-enriched fraction (Memb). ( E ) Lengths, accession numbers and molecular sizes (in kDa) of rat and rabbit channel subunit orthologs currently available in the NCBI protein database. The Kv1.4 sizes are those of unglycosylated forms, which are smaller than the N-glycosylated forms shown in (A). Kv4.2 and Kv4.3 do not have N-glycosylation signals. The rabbit Kv4.3 we detected (∼60 kDa, panel (C), left lane) was likely the short isoform (62.4 kDa). KChIP2 is a cytosolic protein, and thus is not glycosylated.

    Article Snippet: After fractionation, the proteins were blotted to PVDF membranes (Amersham), and probed with the following antibodies: Cav1.2 mAb (NeuroMabs), Cav1.1 mAb (Abcam), Kv4.2 pAb (Sigma), Kv4.3 pAb (Alomone), KChIP2 mAb (NeuroMabs), Kv1.4 mAb (NeuroMabs) and hERG pAb (Alomone).

    Techniques: Western Blot

    ( A ) Immunoblot images of Kv4.2, Kv4.3, and KChIP2 (∼80 ug/lane). ( B ) Immunoblot images of Kv1.4 (∼160 ug/lane). Size marker bands (in kDa) are listed on the left. Sizes for proteins of interest are marked on the right. Note that for panel (A) here and , each channel subunit immunoblot was corrected by its own α-actin immunoblot for loading variations, although only one representative α-actin immunoblot is shown. Loading variation in Fig. 6B was further checked by coomassie blue (CB) stain. ( C ) Data summary: background-subtracted band intensities were divided by corresponding α-actin band intensity, and then normalized by the mean value of control lanes.

    Journal: PLoS ONE

    Article Title: Long-Term Fish Oil Supplementation Induces Cardiac Electrical Remodeling by Changing Channel Protein Expression in the Rabbit Model

    doi: 10.1371/journal.pone.0010140

    Figure Lengend Snippet: ( A ) Immunoblot images of Kv4.2, Kv4.3, and KChIP2 (∼80 ug/lane). ( B ) Immunoblot images of Kv1.4 (∼160 ug/lane). Size marker bands (in kDa) are listed on the left. Sizes for proteins of interest are marked on the right. Note that for panel (A) here and , each channel subunit immunoblot was corrected by its own α-actin immunoblot for loading variations, although only one representative α-actin immunoblot is shown. Loading variation in Fig. 6B was further checked by coomassie blue (CB) stain. ( C ) Data summary: background-subtracted band intensities were divided by corresponding α-actin band intensity, and then normalized by the mean value of control lanes.

    Article Snippet: After fractionation, the proteins were blotted to PVDF membranes (Amersham), and probed with the following antibodies: Cav1.2 mAb (NeuroMabs), Cav1.1 mAb (Abcam), Kv4.2 pAb (Sigma), Kv4.3 pAb (Alomone), KChIP2 mAb (NeuroMabs), Kv1.4 mAb (NeuroMabs) and hERG pAb (Alomone).

    Techniques: Western Blot, Marker, Staining