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protein g dynabeads  (Thermo Fisher)


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    Structured Review

    Thermo Fisher protein g dynabeads
    Protein G Dynabeads, supplied by Thermo Fisher, 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/dynabeads+protein+g/RIPA+buffer/pm42192110-540-9-11
    Average 99 stars, based on 1 article reviews
    protein g dynabeads - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Immunoprecipitation:

    Article Title: Combining light-induced aggregation and biotin proximity labeling implicates endolysosomal proteins in early α-synuclein oligomerization
    Article Snippet: .. Immunoprecipitation was performed using Dynabeads Protein G (Thermofisher, Cat. 10004D) following the manufacturer’s instructions. ..

    Article Title: Female-germline specific protein Sakura interacts with Otu and is crucial for germline stem cell renewal and differentiation and oogenesis
    Article Snippet: .. For anti-FLAG immunoprecipitation, 2 μg of mouse anti-FLAG (1/10,000, Sigma, F1804) was incubated with 50 μL of Dynabeads Protein G (Thermo Fisher, 10004D) for 10 min at room temperature. ..

    other:

    Article Title: Loss of endosomal exchanger NHE6 leads to pathological changes in tau in human neurons
    Article Snippet: NHE6 immunoprecipitation and western blotting iPSCs were lysed 50 mM Tris-HCl, pH 7.8, 137 mM NaCl, 1 mM NaF, 1 mM NaVO3, 1% Triton X-100, 0.2% Sarkosyl, 1 mM dithiothreitol, and 10% glycerol supplemented with protease inhibitor cocktail and phosphatase inhibitor (Roche) for 30 min on ice.

    Incubation:

    Article Title: Female-germline specific protein Sakura interacts with Otu and is crucial for germline stem cell renewal and differentiation and oogenesis
    Article Snippet: .. Four μg of rabbit anti-Sakura and normal rabbit IgG (Cell Signaling, #2729) were incubated with 50 μL of Dynabeads Protein G (Thermo Fisher, 10004D) for 20 min at room temperature. ..

    Article Title: Female-germline specific protein Sakura interacts with Otu and is crucial for germline stem cell renewal and differentiation and oogenesis
    Article Snippet: .. For anti-FLAG immunoprecipitation, 2 μg of mouse anti-FLAG (1/10,000, Sigma, F1804) was incubated with 50 μL of Dynabeads Protein G (Thermo Fisher, 10004D) for 10 min at room temperature. ..

    Suspension:

    Article Title: Forming cytoplasmic stress granules PURα suppresses mRNA translation initiation of IGFBP3 to promote esophageal squamous cell carcinoma progression
    Article Snippet: .. Dynabeads Protein G (Thermo Fisher Scientific) were resuspended thoroughly to obtain a homogeneous suspension, and 50 μl of Dynabeads Protein G were transferred to a 1.5 ml eppendorf tube at room temperature (RT). .. Then, the tube was placed on a magnet for 1 min, the supernatant was discarded, and 1 ml of citrate-phosphate buffer (pH 5.0) was added to wash the Dynabeads Protein G. Then, 10 μg of anti-PURα antibody (Abcam, Cat# ab125200) or rabbit IgG was added to 200 μl of PBS solution with 0.2% Tween, and the resulting mixture was transferred to prepared magnetic beads and incubated for 1.5 h RT with end-over-end rotation.



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    Thermo Fisher dynabeads protein g magnetic beads
    ( A ) Two paralogous ZAD-ZnF genes D19B and D19A are tandemly placed at the locus. ( B ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19A and D19B proteins. Two- to 4-hour embryos from corresponding homozygous strains were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( C ) Measurement of the embryo hatching rate. Embryos from corresponding homozygous full-locus deletion mutant adults were used for the analysis. ( D ) Confocal images of His2Av-emiRFP670 in embryos from WT or homozygous D19B[ Δ 1] mutant adults. The maximum-intensity–projected images of His2Av-emiRFP670 are shown. ( E ) Measurement of the embryo hatching rate. Maternal supply of D19B is essential for the correct progression of embryogenesis. ( F ) Schematic of the full-length D19B protein. ( G ) AlphaFold3 prediction of the D19B ZAD dimer. Protein structure was visualized using UCSF ChimeraX . ( H ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19B and WT/ΔZAD D19B rescue constructs reintroduced into the endogenous locus via recombinase-mediated cassette exchange (RMCE). Two- to 4-hour embryos from corresponding homozygous mutant adults were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( I ) Airyscan imaging of GFP-3xFLAG–tagged WT and ΔZAD D19B expressed from the endogenous locus. Images were taken ~15 min after entry into nc14. Embryos from corresponding homozygous strains were used for the analysis. The maximum-intensity–projected images are shown. ( J ) Measurement of embryo hatching rate. Embryos from corresponding homozygous RMCE strains were used for the analysis.
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    Bimake Inc protein a g coupled dynabeads
    ( A ) Two paralogous ZAD-ZnF genes D19B and D19A are tandemly placed at the locus. ( B ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19A and D19B proteins. Two- to 4-hour embryos from corresponding homozygous strains were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( C ) Measurement of the embryo hatching rate. Embryos from corresponding homozygous full-locus deletion mutant adults were used for the analysis. ( D ) Confocal images of His2Av-emiRFP670 in embryos from WT or homozygous D19B[ Δ 1] mutant adults. The maximum-intensity–projected images of His2Av-emiRFP670 are shown. ( E ) Measurement of the embryo hatching rate. Maternal supply of D19B is essential for the correct progression of embryogenesis. ( F ) Schematic of the full-length D19B protein. ( G ) AlphaFold3 prediction of the D19B ZAD dimer. Protein structure was visualized using UCSF ChimeraX . ( H ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19B and WT/ΔZAD D19B rescue constructs reintroduced into the endogenous locus via recombinase-mediated cassette exchange (RMCE). Two- to 4-hour embryos from corresponding homozygous mutant adults were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( I ) Airyscan imaging of GFP-3xFLAG–tagged WT and ΔZAD D19B expressed from the endogenous locus. Images were taken ~15 min after entry into nc14. Embryos from corresponding homozygous strains were used for the analysis. The maximum-intensity–projected images are shown. ( J ) Measurement of embryo hatching rate. Embryos from corresponding homozygous RMCE strains were used for the analysis.
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    Image Search Results


    ( A ) Two paralogous ZAD-ZnF genes D19B and D19A are tandemly placed at the locus. ( B ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19A and D19B proteins. Two- to 4-hour embryos from corresponding homozygous strains were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( C ) Measurement of the embryo hatching rate. Embryos from corresponding homozygous full-locus deletion mutant adults were used for the analysis. ( D ) Confocal images of His2Av-emiRFP670 in embryos from WT or homozygous D19B[ Δ 1] mutant adults. The maximum-intensity–projected images of His2Av-emiRFP670 are shown. ( E ) Measurement of the embryo hatching rate. Maternal supply of D19B is essential for the correct progression of embryogenesis. ( F ) Schematic of the full-length D19B protein. ( G ) AlphaFold3 prediction of the D19B ZAD dimer. Protein structure was visualized using UCSF ChimeraX . ( H ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19B and WT/ΔZAD D19B rescue constructs reintroduced into the endogenous locus via recombinase-mediated cassette exchange (RMCE). Two- to 4-hour embryos from corresponding homozygous mutant adults were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( I ) Airyscan imaging of GFP-3xFLAG–tagged WT and ΔZAD D19B expressed from the endogenous locus. Images were taken ~15 min after entry into nc14. Embryos from corresponding homozygous strains were used for the analysis. The maximum-intensity–projected images are shown. ( J ) Measurement of embryo hatching rate. Embryos from corresponding homozygous RMCE strains were used for the analysis.

    Journal: Science Advances

    Article Title: Decoding the molecular logic of rapidly evolving ZAD zinc finger proteins in Drosophila

    doi: 10.1126/sciadv.ady7568

    Figure Lengend Snippet: ( A ) Two paralogous ZAD-ZnF genes D19B and D19A are tandemly placed at the locus. ( B ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19A and D19B proteins. Two- to 4-hour embryos from corresponding homozygous strains were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( C ) Measurement of the embryo hatching rate. Embryos from corresponding homozygous full-locus deletion mutant adults were used for the analysis. ( D ) Confocal images of His2Av-emiRFP670 in embryos from WT or homozygous D19B[ Δ 1] mutant adults. The maximum-intensity–projected images of His2Av-emiRFP670 are shown. ( E ) Measurement of the embryo hatching rate. Maternal supply of D19B is essential for the correct progression of embryogenesis. ( F ) Schematic of the full-length D19B protein. ( G ) AlphaFold3 prediction of the D19B ZAD dimer. Protein structure was visualized using UCSF ChimeraX . ( H ) Western blot analysis of GFP-3xFLAG–tagged endogenous D19B and WT/ΔZAD D19B rescue constructs reintroduced into the endogenous locus via recombinase-mediated cassette exchange (RMCE). Two- to 4-hour embryos from corresponding homozygous mutant adults were used for the analysis. As a control, 2- to 4-hour yw embryos were used. ( I ) Airyscan imaging of GFP-3xFLAG–tagged WT and ΔZAD D19B expressed from the endogenous locus. Images were taken ~15 min after entry into nc14. Embryos from corresponding homozygous strains were used for the analysis. The maximum-intensity–projected images are shown. ( J ) Measurement of embryo hatching rate. Embryos from corresponding homozygous RMCE strains were used for the analysis.

    Article Snippet: Dynabeads Protein G magnetic beads (Invitrogen) were diluted by adding 10 μl of beads to 100 μl of blocking solution [PBS containing bovine serum albumin (BSA; 5 mg/ml)].

    Techniques: Western Blot, Control, Mutagenesis, Construct, Imaging