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laser scanning confocal microscopy image data  (Oxford Instruments)


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    Oxford Instruments laser scanning confocal microscopy image data
    (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) <t>Microscopy</t> from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm
    Laser Scanning Confocal Microscopy Image Data, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44474 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/laser+scanning+confocal+microscopy+image+data/Imaris/bio_rxiv__64898__2026__02__18__706625-498-10-19
    Average 99 stars, based on 44474 article reviews
    laser scanning confocal microscopy image data - by Bioz Stars, 2026-10
    99/100 stars

    Images

    1) Product Images from "Weckle is a molecular switch that diverts Toll signalling from innate immunity towards growth by engaging Yki"

    Article Title: Weckle is a molecular switch that diverts Toll signalling from innate immunity towards growth by engaging Yki

    Journal: bioRxiv

    doi: 10.64898/2026.02.18.706625

    (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) Microscopy from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm
    Figure Legend Snippet: (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) Microscopy from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm

    Techniques Used: Mass Spectrometry, Purification, Transfection, Mutagenesis, Western Blot, Migration, Modification, Cotransfection, Microscopy, Phospho-proteomics, Translocation Assay

    Related Articles

    Membrane:

    Article Title: Weckle is a molecular switch that diverts Toll signalling from innate immunity towards growth by engaging Yki
    Article Snippet: .. To analyse glial cell membrane volume in adult antennal lobes, laser scanning confocal microscopy image data were processed with Imaris using the “Surface” module. ..

    Confocal Microscopy:

    Article Title: Weckle is a molecular switch that diverts Toll signalling from innate immunity towards growth by engaging Yki
    Article Snippet: .. To analyse glial cell membrane volume in adult antennal lobes, laser scanning confocal microscopy image data were processed with Imaris using the “Surface” module. ..



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    laser scanning confocal microscopy image data  (Oxford Instruments)
    99
    Oxford Instruments laser scanning confocal microscopy image data
    (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) <t>Microscopy</t> from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm
    Laser Scanning Confocal Microscopy Image Data, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/laser+scanning+confocal+microscopy+image+data/Imaris/bio_rxiv__64898__2026__02__18__706625-498-10-19
    Average 99 stars, based on 1 article reviews
    laser scanning confocal microscopy image data - by Bioz Stars, 2026-10
    99/100 stars
    		  Buy from Supplier

    Image Search Results


    (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) Microscopy from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm

    Journal: bioRxiv

    Article Title: Weckle is a molecular switch that diverts Toll signalling from innate immunity towards growth by engaging Yki

    doi: 10.64898/2026.02.18.706625

    Figure Lengend Snippet: (A) Diagram of Glycine2 and Serines in Wek tested. (B) Mass spectrometry of purified Wek-FLAG: S2 cells were co-transfected with wek-FLAG and Toll-6HA, or wek-FLAG and pelle-HA and stimulated with purified DNT-2, Wek was purified, and found to be phosphorylated at Ser164. This Ser was not phosphorylated in controls. (C,D) Phostag gel of wek mutant forms expressed in S2 cells, showing: (C) western blot input; (D) Phostag gel, showing the distinct migration profile of the Wek mutant forms. Asterisks indicate bands modified by the co-transfection with Pelle. (E,F) Microscopy from transfected S2 cells showing that site directed mutagenesis of wek in G2A, S164A and S168A, alter the subcellular distribution of Wek, and this is further influenced by pelle . Wek visualised with anti-FLAG antibodies (green) and nuclei with DAPI (magenta). (G) Illustration showing that phosphorylation at Ser6 and Ser168 are required for the nuclear translocation of Wek. Scale bar: (E,F) 10μm

    Article Snippet: To analyse glial cell membrane volume in adult antennal lobes, laser scanning confocal microscopy image data were processed with Imaris using the “Surface” module.

    Techniques: Mass Spectrometry, Purification, Transfection, Mutagenesis, Western Blot, Migration, Modification, Cotransfection, Microscopy, Phospho-proteomics, Translocation Assay