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anti ikca  (Alomone Labs)


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    Alomone Labs anti ikca
    Anti Ikca, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 95/100, based on 70 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+ikca/Anti-KCNN4+(KCa3%2E1%2C+SK4)+Antibody/pmc12623187-227-10-13
    Average 95 stars, based on 70 article reviews
    anti ikca - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Differential participation of calcium-activated potassium channel in endothelium-dependent hyperpolarization-type relaxation in superior mesenteric arteries of spontaneously hypertensive rats.
    Article Snippet: The purpose of this study was to determine the relationship of KCa channels to endothelium-dependent hyperpolarizing factor (EDHF)-mediated relaxation induced by acetylcholine (ACh) in the superior mesenteric arteries of 7-month-old spontaneously hypertensive rats (SHR).. Upon inhibition of nitric oxide synthase and cyclooxygenase, ACh-induced EDHF-mediated relaxation was found to be weaker in SHR than in age-matched Wistar Kyoto rats (WKY).. These relaxations in both group were attenuated by combined treatment with small-conductance and intermediate-conductance Ca-activated K channels (SKCa and IKCa) inhibitors, with the exception of relaxation resistant to inhibition of these channels in SHR (vs. WKY).

    Incubation:

    Article Title: Differential participation of calcium-activated potassium channel in endothelium-dependent hyperpolarization-type relaxation in superior mesenteric arteries of spontaneously hypertensive rats.
    Article Snippet: The purpose of this study was to determine the relationship of KCa channels to endothelium-dependent hyperpolarizing factor (EDHF)-mediated relaxation induced by acetylcholine (ACh) in the superior mesenteric arteries of 7-month-old spontaneously hypertensive rats (SHR).. Upon inhibition of nitric oxide synthase and cyclooxygenase, ACh-induced EDHF-mediated relaxation was found to be weaker in SHR than in age-matched Wistar Kyoto rats (WKY).. These relaxations in both group were attenuated by combined treatment with small-conductance and intermediate-conductance Ca-activated K channels (SKCa and IKCa) inhibitors, with the exception of relaxation resistant to inhibition of these channels in SHR (vs. WKY).



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    Expression of KCa channels in human villus tissues. Immunohistochemical detection of different types of KCa <t>channels</t> <t>(BKCa</t> α, BKCa β1, <t>IKCa,</t> and SKCa) and the negative control in human villus tissues.
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    FIGURE 2 Stiff substrates upregulate the <t>IKCa</t> channel expression in A7r5 VSMCs. (a, b) Representative images showing the IKCa mRNA expression using RT‐PCR and IKCa protein cell surface expression using flow cytometry. (c) Summary of the mean data from 4 independent experiments. *p < .05; **p < .01. GAPDH, glyceraldehyde 3‐phosphate dehydrogenase; IKCa, intermediate‐conductance Ca2+‐activated K+; mRNA, messenger RNA; RT‐PCR, reverse‐transcription polymerase chain reaction;VSMC, vascular smooth muscle cell
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    Image Search Results


    Expression of KCa channels in human villus tissues. Immunohistochemical detection of different types of KCa channels (BKCa α, BKCa β1, IKCa, and SKCa) and the negative control in human villus tissues.

    Journal: Open Life Sciences

    Article Title: Effects of KCa channels on biological behavior of trophoblasts

    doi: 10.1515/biol-2022-0462

    Figure Lengend Snippet: Expression of KCa channels in human villus tissues. Immunohistochemical detection of different types of KCa channels (BKCa α, BKCa β1, IKCa, and SKCa) and the negative control in human villus tissues.

    Article Snippet: The primary antibodies included rabbit anti-BKCa α (APC-107, 1:100), BKCa β1 (APC-036, 1:100), IKCa (APC-064, 1:100), and SKCa (APC-025, 1:100), all of which were provided by Alomone Labs Company in Israel.

    Techniques: Expressing, Immunohistochemical staining, Negative Control, Immunohistochemistry

    Localization and expression of KCa channels in HTR-8/SVneo cells. BKCa α and β1 subunits, IKCa channels, SKCa channels, and the control in HTR-8/SVneo cells were observed under the fluorescence microscope. Cells were stained with DAPI to visualize nucleus (blue) and immunolabeled with Anti-KCa antibodies (green), respectively. Arrow indicates the positive staining.

    Journal: Open Life Sciences

    Article Title: Effects of KCa channels on biological behavior of trophoblasts

    doi: 10.1515/biol-2022-0462

    Figure Lengend Snippet: Localization and expression of KCa channels in HTR-8/SVneo cells. BKCa α and β1 subunits, IKCa channels, SKCa channels, and the control in HTR-8/SVneo cells were observed under the fluorescence microscope. Cells were stained with DAPI to visualize nucleus (blue) and immunolabeled with Anti-KCa antibodies (green), respectively. Arrow indicates the positive staining.

    Article Snippet: The primary antibodies included rabbit anti-BKCa α (APC-107, 1:100), BKCa β1 (APC-036, 1:100), IKCa (APC-064, 1:100), and SKCa (APC-025, 1:100), all of which were provided by Alomone Labs Company in Israel.

    Techniques: Expressing, Control, Fluorescence, Microscopy, Staining, Immunolabeling, Immunofluorescence

    FIGURE 2 Stiff substrates upregulate the IKCa channel expression in A7r5 VSMCs. (a, b) Representative images showing the IKCa mRNA expression using RT‐PCR and IKCa protein cell surface expression using flow cytometry. (c) Summary of the mean data from 4 independent experiments. *p < .05; **p < .01. GAPDH, glyceraldehyde 3‐phosphate dehydrogenase; IKCa, intermediate‐conductance Ca2+‐activated K+; mRNA, messenger RNA; RT‐PCR, reverse‐transcription polymerase chain reaction;VSMC, vascular smooth muscle cell

    Journal: Journal of cellular physiology

    Article Title: Stimulation of vascular smooth muscle cell proliferation by stiff matrix via the IK Ca channel-dependent Ca 2+ signaling.

    doi: 10.1002/jcp.30349

    Figure Lengend Snippet: FIGURE 2 Stiff substrates upregulate the IKCa channel expression in A7r5 VSMCs. (a, b) Representative images showing the IKCa mRNA expression using RT‐PCR and IKCa protein cell surface expression using flow cytometry. (c) Summary of the mean data from 4 independent experiments. *p < .05; **p < .01. GAPDH, glyceraldehyde 3‐phosphate dehydrogenase; IKCa, intermediate‐conductance Ca2+‐activated K+; mRNA, messenger RNA; RT‐PCR, reverse‐transcription polymerase chain reaction;VSMC, vascular smooth muscle cell

    Article Snippet: Following three washes with PBS, cells were incubated with a pri- mary mouse antibody specifically against the IKCa extracellular domain (ALM051, 1:100; Alomone Labs) for 40min.

    Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Flow Cytometry, Reverse Transcription, Polymerase Chain Reaction

    FIGURE 3 Stiff substrate‐induced IKCa channel upregulation is required for increased A7r5 VSMC proliferation. (a) Summary of the effects of treatment with 100 nM TRAM34 on stiff substrate‐induced cell proliferation from three independent experiments. (b) Representative western blots showing siRNA‐mediated knockdown of the IKCa protein expression (top) and summary of the data from five independent experiments (bottom). (c) Summary of stiff substrate‐induced cell proliferation in siRNA‐transfected cells from three independent experiments. *p < .05 and **p < .01 compared between 0.21 and 1.72 MPa without any treatment or compared between 1.72 MPa with or without treatment with TRAM34, respectively. IKCa, intermediate‐conductance Ca2+‐activated K+; siRNA, small interfering RNA; VSMC, vascular smooth muscle cell

    Journal: Journal of cellular physiology

    Article Title: Stimulation of vascular smooth muscle cell proliferation by stiff matrix via the IK Ca channel-dependent Ca 2+ signaling.

    doi: 10.1002/jcp.30349

    Figure Lengend Snippet: FIGURE 3 Stiff substrate‐induced IKCa channel upregulation is required for increased A7r5 VSMC proliferation. (a) Summary of the effects of treatment with 100 nM TRAM34 on stiff substrate‐induced cell proliferation from three independent experiments. (b) Representative western blots showing siRNA‐mediated knockdown of the IKCa protein expression (top) and summary of the data from five independent experiments (bottom). (c) Summary of stiff substrate‐induced cell proliferation in siRNA‐transfected cells from three independent experiments. *p < .05 and **p < .01 compared between 0.21 and 1.72 MPa without any treatment or compared between 1.72 MPa with or without treatment with TRAM34, respectively. IKCa, intermediate‐conductance Ca2+‐activated K+; siRNA, small interfering RNA; VSMC, vascular smooth muscle cell

    Article Snippet: Following three washes with PBS, cells were incubated with a pri- mary mouse antibody specifically against the IKCa extracellular domain (ALM051, 1:100; Alomone Labs) for 40min.

    Techniques: Western Blot, Knockdown, Expressing, Transfection, Small Interfering RNA

    FIGURE 4 Stiff substrate induces IKCa‐ dependent increase in [Ca2+]i in A7r5 VSMCs. (a) Representative single‐cell images showing intracellular Ca2+ concentration in cells cultured on the soft and stiff substrate under indicated conditions. Treatment with 100 nM TRAM34 was made during culture media and also in extracellular recording solution. (b) Summary of the relative Fluo4 fluorescence intensity, indicative of the [Ca2+]i, in individual cells under the condition shown in (a), with 375 cells examined for each case. **p < .01. IKCa, intermediate‐conductance Ca2+‐activated K+; VSMC, vascular smooth muscle cell

    Journal: Journal of cellular physiology

    Article Title: Stimulation of vascular smooth muscle cell proliferation by stiff matrix via the IK Ca channel-dependent Ca 2+ signaling.

    doi: 10.1002/jcp.30349

    Figure Lengend Snippet: FIGURE 4 Stiff substrate induces IKCa‐ dependent increase in [Ca2+]i in A7r5 VSMCs. (a) Representative single‐cell images showing intracellular Ca2+ concentration in cells cultured on the soft and stiff substrate under indicated conditions. Treatment with 100 nM TRAM34 was made during culture media and also in extracellular recording solution. (b) Summary of the relative Fluo4 fluorescence intensity, indicative of the [Ca2+]i, in individual cells under the condition shown in (a), with 375 cells examined for each case. **p < .01. IKCa, intermediate‐conductance Ca2+‐activated K+; VSMC, vascular smooth muscle cell

    Article Snippet: Following three washes with PBS, cells were incubated with a pri- mary mouse antibody specifically against the IKCa extracellular domain (ALM051, 1:100; Alomone Labs) for 40min.

    Techniques: Single Cell, Concentration Assay, Cell Culture, Fluorescence

    FIGURE 5 Stiff substrate‐induced IKCa channel‐dependent increases in [Ca2+]i is essential for increased A7r5 VSMC proliferation. Summary of cell proliferation on substrates in culture media containing (a) 1 mM EGTA or (b) 10 μM BAPTA‐AM, from three independent experiments for each case. **p < .01. EGTA, ethylene glycol‐bis(β‐aminoethyl ether)‐N,N,N′,N′‐tetraacetic acid; IKCa, intermediate‐conductance Ca2+‐activated K+; VSMC, vascular smooth muscle cell

    Journal: Journal of cellular physiology

    Article Title: Stimulation of vascular smooth muscle cell proliferation by stiff matrix via the IK Ca channel-dependent Ca 2+ signaling.

    doi: 10.1002/jcp.30349

    Figure Lengend Snippet: FIGURE 5 Stiff substrate‐induced IKCa channel‐dependent increases in [Ca2+]i is essential for increased A7r5 VSMC proliferation. Summary of cell proliferation on substrates in culture media containing (a) 1 mM EGTA or (b) 10 μM BAPTA‐AM, from three independent experiments for each case. **p < .01. EGTA, ethylene glycol‐bis(β‐aminoethyl ether)‐N,N,N′,N′‐tetraacetic acid; IKCa, intermediate‐conductance Ca2+‐activated K+; VSMC, vascular smooth muscle cell

    Article Snippet: Following three washes with PBS, cells were incubated with a pri- mary mouse antibody specifically against the IKCa extracellular domain (ALM051, 1:100; Alomone Labs) for 40min.

    Techniques: