kir 4 1  (Alomone Labs)


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    Alomone Labs kir 4 1
    Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.
    Kir 4 1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kir 4 1/product/Alomone Labs
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kir 4 1 - by Bioz Stars, 2023-01
    96/100 stars

    Images

    1) Product Images from "Pathophysiological Characteristics Associated With Epileptogenesis in Human Hippocampal Sclerosis"

    Article Title: Pathophysiological Characteristics Associated With Epileptogenesis in Human Hippocampal Sclerosis

    Journal: EBioMedicine

    doi: 10.1016/j.ebiom.2018.02.013

    Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.
    Figure Legend Snippet: Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.

    Techniques Used: Immunofluorescence

    subunit pp 1c  (Alomone Labs)


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    Alomone Labs subunit pp 1c
    Subunit Pp 1c, 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/subunit pp 1c/product/Alomone Labs
    Average 86 stars, based on 1 article reviews
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    subunit pp 1c - by Bioz Stars, 2023-01
    86/100 stars

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    kir 4 1  (Alomone Labs)


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    Alomone Labs kir 4 1
    Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.
    Kir 4 1, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/kir 4 1/product/Alomone Labs
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    kir 4 1 - by Bioz Stars, 2023-01
    96/100 stars

    Images

    1) Product Images from "Pathophysiological Characteristics Associated With Epileptogenesis in Human Hippocampal Sclerosis"

    Article Title: Pathophysiological Characteristics Associated With Epileptogenesis in Human Hippocampal Sclerosis

    Journal: EBioMedicine

    doi: 10.1016/j.ebiom.2018.02.013

    Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.
    Figure Legend Snippet: Different responses to potassium concentrations in the subiculum of the HS and No-HS groups. (a) Number ( left ) and amplitude ( right ) of events during 10-min LFP recordings in the presence of 6, 9, and 12 mM [K + ] o are normalized to those recorded in the presence of 3 mM [K + ] o . (b) Representative images of time-frequency power-spectral analysis of 10 averaged consecutive events with changes in [K + ] o . Note the ascending spots in HS. Scale bar: 100 ms. (c) Quantification of changing the frequencies at peak power in the presence of 3, 6, 9, and 12 mM [K + ] o . (a–c) In these studies, we used two slices per patient. ( n ) indicates the number of slices. *p < .05, Tukey-Kramer test after one-factor ANOVA. (d) Double immunofluorescence images of the subiculum indicating loss of Kir 4.1 immunoreactivity ( red ) in the processes of GFAP ( green )-positive cells in HS. Scale bar: 50 μm. (e) Quantitative analysis of the total area of immunofluorescence. The immunofluorescence area of Kir4.1 was normalized to that of GFAP. *p < 0.05, Tukey-Kramer test after one-factor ANOVA. Lower panels are sample images of the original image (upper) and the extracted area for calculation (Red area: lower). Scale bars: 25 μm. Error bars, S.E.M.

    Techniques Used: Immunofluorescence

    7 10a dimethano 10ah  (Alomone Labs)


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    Alomone Labs 7 10a dimethano 10ah
    7 10a Dimethano 10ah, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 85 stars, based on 1 article reviews
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    7 10a dimethano 10ah - by Bioz Stars, 2023-01
    85/100 stars

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    primary antibody fluorescent dye asic3 rabbit anti human asic3 antibody  (Alomone Labs)


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    Alomone Labs primary antibody fluorescent dye asic3 rabbit anti human asic3 antibody
    Primary Antibody Fluorescent Dye Asic3 Rabbit Anti Human Asic3 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
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    Average 86 stars, based on 1 article reviews
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    86/100 stars

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    ly 294002  (Alomone Labs)


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    Alomone Labs ly 294002
    Ly 294002, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 1 article reviews
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    u 73122  (Alomone Labs)


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    Alomone Labs u 73122
    U 73122, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    tissue for immunobuffer  (Alomone Labs)


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    Alomone Labs tissue for immunobuffer
    Tissue For Immunobuffer, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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