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rabbit anti tgoln2  (Bethyl)


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    Structured Review

    Bethyl rabbit anti tgoln2
    Rabbit Anti Tgoln2, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+tgoln2/bio_rxiv__2025__09__05__674545-271-23-25?v=Bethyl
    Average 93 stars, based on 2 article reviews
    rabbit anti tgoln2 - by Bioz Stars, 2026-07
    93/100 stars

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    The R1771C apo(a) shows a reduced progression through the secretory pathway. HepG2 cells were transfected with 500 ng of either WT or R1771C apo(a)-GFP cDNA and fixed and imaged by confocal microscopy at 24 h. Cells were permeabilized and stained with antibodies for apo(a), the ER protein, calnexin, the CopII protein, Sec31A, and the Golgi marker protein, <t>TGOLN2.</t> The apo(a) antibody was detected with an anti-mouse Alexa Fluor® 647 secondary antibody (blue), the calnexin, the Sec31A and TGOLN2 antibodies were detected with an anti-rabbit Alexa Fluor® 555 secondary antibody (red). Multiple fields of view were visualized and representative images are shown. Images are also shown as overlays with a DAPI nuclear stain (cyan). Colocalization of the Alexa Fluor® 647 signal detecting apo(a) with the Alexa Fluor® 555 signal detecting the various compartment markers was assessed in confocal images of transfected cells by calculating the Pearson’s correlation coefficient using the Colocalization Finder plugin of ImageJ. Data represents mean ± SEM for at least fifteen individual cells. **P < 0.01 for R1771C versus WT apo(a).
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    Image Search Results


    Reagents and tools table

    Journal: The EMBO Journal

    Article Title: A novel biosensor for the spatiotemporal analysis of STING activation during innate immune responses to dsDNA

    doi: 10.1038/s44318-025-00370-y

    Figure Lengend Snippet: Reagents and tools table

    Article Snippet: Rabbit anti-TGOLN2 , Cell Signaling Technologies , 55727.

    Techniques: Mutagenesis, Expressing, Recombinant, Sequencing, Cloning, Software

    Reagents and tools table

    Journal: The EMBO Journal

    Article Title: Non-autophagic Golgi-LC3 lipidation facilitates TFE3 stress response against Golgi dysfunction

    doi: 10.1038/s44318-024-00233-y

    Figure Lengend Snippet: Reagents and tools table

    Article Snippet: Rabbit monoclonal anti-TGOLN2 , Abclonal , Cat # A19618;.

    Techniques: Recombinant, Sequencing, Virus, Reverse Transcription, SYBR Green Assay, Protease Inhibitor, Software

    The R1771C apo(a) shows a reduced progression through the secretory pathway. HepG2 cells were transfected with 500 ng of either WT or R1771C apo(a)-GFP cDNA and fixed and imaged by confocal microscopy at 24 h. Cells were permeabilized and stained with antibodies for apo(a), the ER protein, calnexin, the CopII protein, Sec31A, and the Golgi marker protein, TGOLN2. The apo(a) antibody was detected with an anti-mouse Alexa Fluor® 647 secondary antibody (blue), the calnexin, the Sec31A and TGOLN2 antibodies were detected with an anti-rabbit Alexa Fluor® 555 secondary antibody (red). Multiple fields of view were visualized and representative images are shown. Images are also shown as overlays with a DAPI nuclear stain (cyan). Colocalization of the Alexa Fluor® 647 signal detecting apo(a) with the Alexa Fluor® 555 signal detecting the various compartment markers was assessed in confocal images of transfected cells by calculating the Pearson’s correlation coefficient using the Colocalization Finder plugin of ImageJ. Data represents mean ± SEM for at least fifteen individual cells. **P < 0.01 for R1771C versus WT apo(a).

    Journal: Journal of Lipid Research

    Article Title: Nonsynonymous SNPs in LPA homologous to plasminogen deficiency mutants represent novel null apo(a) alleles [S]

    doi: 10.1194/jlr.M094540

    Figure Lengend Snippet: The R1771C apo(a) shows a reduced progression through the secretory pathway. HepG2 cells were transfected with 500 ng of either WT or R1771C apo(a)-GFP cDNA and fixed and imaged by confocal microscopy at 24 h. Cells were permeabilized and stained with antibodies for apo(a), the ER protein, calnexin, the CopII protein, Sec31A, and the Golgi marker protein, TGOLN2. The apo(a) antibody was detected with an anti-mouse Alexa Fluor® 647 secondary antibody (blue), the calnexin, the Sec31A and TGOLN2 antibodies were detected with an anti-rabbit Alexa Fluor® 555 secondary antibody (red). Multiple fields of view were visualized and representative images are shown. Images are also shown as overlays with a DAPI nuclear stain (cyan). Colocalization of the Alexa Fluor® 647 signal detecting apo(a) with the Alexa Fluor® 555 signal detecting the various compartment markers was assessed in confocal images of transfected cells by calculating the Pearson’s correlation coefficient using the Colocalization Finder plugin of ImageJ. Data represents mean ± SEM for at least fifteen individual cells. **P < 0.01 for R1771C versus WT apo(a).

    Article Snippet: In a separate experiment, cells were incubated with a mouse anti-apo(a) antibody (LPA4, MABS1284; Sigma-Aldrich) and either a rabbit anti-calnexin antibody, a rabbit anti-Sec31A antibody (ab86600; Abcam), or a rabbit anti- trans -Golgi network 2 (TGOLN2) antibody (Sigma).

    Techniques: Transfection, Confocal Microscopy, Staining, Marker