optimus primer Search Results


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Thermo Fisher optimal dna primers
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Revvity ivis spectrum instrument
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Revvity ivis spectrum
Knockout of AMPKα promotes DAOY proliferation. A Western blot detection of AMPKα protein level in PRKAA1 +/+ and PRKAA1 −/− DAOYs. B Proliferation of PRKAA1 +/+ and PRKAA1 −/− DAOYs were assessed by CCK-8. *** P < 0.001. C Western blot detection of AMPKα protein level in PRKAA1 −/− DAOYs transfected with PRKAA1 cDNA. D Cell viability of transfected PRKAA1 −/− DAOYs was detected by CCK-8. ** P < 0.01. E Tumorsphere formation ability was detected by extreme limiting dilution assays. F Representative images of tumorspheres formed by PRKAA1 +/+ and PRKAA1 . −/− DAOYs. G Quantification of the number of spheres (per 5000 cells) formed by DAOYs. Data in bar graphs are presented as mean ± SEM from three independent experiments. ** P < 0.01. H The time course of in vivo fluorescence images of NOD-SCID mice implanted with DAOY-Luc cells in the cerebellum using <t>IVIS</t> Spectrum In Vivo Imaging System. I Quantification of total Flux of mice. ** P < 0.01. J HE staining and K IHC staining of Ki67 of cerebellar tumors generated by implanting DAOY-Luc cells (5 × and 40x)
Ivis Spectrum, supplied by Revvity, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Knockout of AMPKα promotes DAOY proliferation. A Western blot detection of AMPKα protein level in PRKAA1 +/+ and PRKAA1 −/− DAOYs. B Proliferation of PRKAA1 +/+ and PRKAA1 −/− DAOYs were assessed by CCK-8. *** P < 0.001. C Western blot detection of AMPKα protein level in PRKAA1 −/− DAOYs transfected with PRKAA1 cDNA. D Cell viability of transfected PRKAA1 −/− DAOYs was detected by CCK-8. ** P < 0.01. E Tumorsphere formation ability was detected by extreme limiting dilution assays. F Representative images of tumorspheres formed by PRKAA1 +/+ and PRKAA1 . −/− DAOYs. G Quantification of the number of spheres (per 5000 cells) formed by DAOYs. Data in bar graphs are presented as mean ± SEM from three independent experiments. ** P < 0.01. H The time course of in vivo fluorescence images of NOD-SCID mice implanted with DAOY-Luc cells in the cerebellum using IVIS Spectrum In Vivo Imaging System. I Quantification of total Flux of mice. ** P < 0.01. J HE staining and K IHC staining of Ki67 of cerebellar tumors generated by implanting DAOY-Luc cells (5 × and 40x)

Journal: Cell & Bioscience

Article Title: AMPK attenuates SHH subgroup medulloblastoma growth and metastasis by inhibiting NF-κB activation

doi: 10.1186/s13578-023-00963-2

Figure Lengend Snippet: Knockout of AMPKα promotes DAOY proliferation. A Western blot detection of AMPKα protein level in PRKAA1 +/+ and PRKAA1 −/− DAOYs. B Proliferation of PRKAA1 +/+ and PRKAA1 −/− DAOYs were assessed by CCK-8. *** P < 0.001. C Western blot detection of AMPKα protein level in PRKAA1 −/− DAOYs transfected with PRKAA1 cDNA. D Cell viability of transfected PRKAA1 −/− DAOYs was detected by CCK-8. ** P < 0.01. E Tumorsphere formation ability was detected by extreme limiting dilution assays. F Representative images of tumorspheres formed by PRKAA1 +/+ and PRKAA1 . −/− DAOYs. G Quantification of the number of spheres (per 5000 cells) formed by DAOYs. Data in bar graphs are presented as mean ± SEM from three independent experiments. ** P < 0.01. H The time course of in vivo fluorescence images of NOD-SCID mice implanted with DAOY-Luc cells in the cerebellum using IVIS Spectrum In Vivo Imaging System. I Quantification of total Flux of mice. ** P < 0.01. J HE staining and K IHC staining of Ki67 of cerebellar tumors generated by implanting DAOY-Luc cells (5 × and 40x)

Article Snippet: Bioluminescence imaging was performed weekly using IVIS Spectrum (Perkin Elmer).

Techniques: Knock-Out, Western Blot, CCK-8 Assay, Transfection, In Vivo, Fluorescence, In Vivo Imaging, Staining, Immunohistochemistry, Generated