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cytokeratin 14 ck 14  (Proteintech)


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    Structured Review

    Proteintech cytokeratin 14 ck 14
    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
    Cytokeratin 14 Ck 14, supplied by Proteintech, used in various techniques. Bioz Stars score: 97/100, based on 163 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cytokeratin 14 ck 14/product/Proteintech
    Average 97 stars, based on 163 article reviews
    cytokeratin 14 ck 14 - by Bioz Stars, 2026-03
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    Images

    1) Product Images from "Insulin-Regulated Actin Dynamics is Disrupted in a Human Keratinocyte Model of Hailey Hailey Disease"

    Article Title: Insulin-Regulated Actin Dynamics is Disrupted in a Human Keratinocyte Model of Hailey Hailey Disease

    Journal: bioRxiv

    doi: 10.64898/2025.12.15.694174

    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) CK-14 immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
    Figure Legend Snippet: Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) CK-14 immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.

    Techniques Used: Immunofluorescence, Control, Staining, Expressing, Labeling, Mutagenesis, Transmission Assay, Membrane



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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) <t>CK-14</t> immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.
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    Image Search Results


    Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) CK-14 immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.

    Journal: bioRxiv

    Article Title: Insulin-Regulated Actin Dynamics is Disrupted in a Human Keratinocyte Model of Hailey Hailey Disease

    doi: 10.64898/2025.12.15.694174

    Figure Lengend Snippet: Representative immunofluorescence images of (a) Dsg-1 showing strong peripheral localization in control keratinocytes, but markedly reduced or absent staining in SPCA1 -/- and SPCA1 +/− cells. Magnification, 20x. Scale bar = 20 μm; (b) E-cadherin immunofluorescence showing robust expression at cell junctions in control keratinocytes but near absence in SPCA1 mutants. Magnification, 20x. Scale bar = 20 μm; (c) CK-14 immunofluorescence revealing prominent perinuclear keratin bundles in SPCA1 −/− keratinocytes, with fewer aggregates in SPCA1 +/- cells. Magnification, 40x. Scale bar = 10 μm; and (d) F-actin labeled with fluorescent phalloidin demonstrates abnormal peripheral actin accumulation and cytoplasmic actin-rich structures in SPCA1 mutant cells. Magnification, 40x. Scale bar = 10 μm. (e) Transmission electron micrographs showing intercellular gaps (black arrows), membrane blebs (asterisks) and keratin bundles (red arrowheads) in SPCA1 mutant cells compared to intact junctions (white arrows) in hTERT control. N, nucleus. Scale bar = 2 μm.

    Article Snippet: Primary antibodies against ATP2C1, GM130, Cytokeratin 14 (CK-14) (Proteintech #60320) and E-cad were incubated overnight at 4°C or at least 1 h at RT in the blocking buffer at 1:50, 1:300, 1:100 and 1:100 dilution, respectively.

    Techniques: Immunofluorescence, Control, Staining, Expressing, Labeling, Mutagenesis, Transmission Assay, Membrane