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Full length Clone DNA of Mouse cleavage and polyadenylation specificity factor 3
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Bethyl
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Proteintech
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qSTAR qPCR primer pairs against Mus musculus gene Cpsf7
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Cpsf7 Mouse 4 unique 29mer shRNA constructs in retroviral untagged vector
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Full length Clone DNA of Mouse cleavage and polyadenylation specificity factor 3
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Cpsf7 CRISPRa kit CRISPR gene activation of mouse cleavage and polyadenylation specific factor 7
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Full length Clone DNA of Mouse cleavage and polyadenylation specificity factor 3 with N terminal GFPSpark tag.
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Image Search Results
Journal: eLife
Article Title: HIV-1 nuclear import in macrophages is regulated by CPSF6-capsid interactions at the nuclear pore complex
doi: 10.7554/eLife.41800
Figure Lengend Snippet:
Article Snippet: Antibody , Rabbit polyclonal anti-hCPSF7 ,
Techniques: Enzyme-linked Immunosorbent Assay, Imaging, Reverse Transcription, Recombinant, Plasmid Preparation, Expressing, shRNA, Control, Software
Journal: Scientific reports
Article Title: Formation of nuclear CPSF6/CPSF5 biomolecular condensates upon HIV-1 entry into the nucleus is important for productive infection.
doi: 10.1038/s41598-023-37364-x
Figure Lengend Snippet: Figure 6. HIV-1 infection induces the formation of CPSF5 condensates that colocalize with CPSF6. A549 cells were infected or not (mock) with HIV-1-Luc at an MOI of ~ 2 for 24 h (A and B). Cells were fixed, permeabilized, and coimmunostained using rabbit polyclonal antibody to CPSF6 with mouse monoclonal antibody against CPSF5 (A) or with mouse monoclonal antibody against CPSF7 (B). Secondary antibodies were Alexa-488-conjugated donkey anti-mouse IgG (green channel) and Alexa-594-conjugated donkey anti-rabbit IgG (red channel). Stained cells were examined by fluorescence microscopy. Merging the red and green channels generated the third image in each row; yellow indicates overlapping localization of the red and green channels. Experiments were repeated at least three times, and a representative experiment is shown. Scale bar = 10 μm.
Article Snippet: We used the following mouse monoclonal antibodies: clone SC-35 against SC35 (Cat# ab11826, Abcam), clone 3F8 against CPSF5 (Cat# H00011051-M12, Novus Biologicals), clone
Techniques: Infection, Staining, Fluorescence, Microscopy, Generated
Journal: Scientific reports
Article Title: Formation of nuclear CPSF6/CPSF5 biomolecular condensates upon HIV-1 entry into the nucleus is important for productive infection.
doi: 10.1038/s41598-023-37364-x
Figure Lengend Snippet: Figure 7. HIV-1 infection induces the formation of CPSF6 and CPSF5 condensates in human T cells and human primary macrophages. Jurkat T cells (A) and macrophages (B) were infected or not (mock) with HIV- 1-GFP at an MOI of ~ 2 for 48 or 72 h, respectively. At 48hpi, 2,5 × 105 Jurkat cells were seeded on glass coverslips previously treated with poly-D-lysine for 1 h. Cells were fixed, permeabilized, and immunostained using rabbit polyclonal antibody to CPSF6, mouse monoclonal antibody against CPSF5 or mouse monoclonal antibody against CPSF7. Secondary antibody was Alexa-594-conjugated donkey anti-rabbit IgG (red channel). Nuclei were stained with DAPI (blue channel). Stained cells were examined by fluorescence microscopy. Merging the red and blue channels generated the third image in each row; magenta indicates overlapping of the red and blue channels. Experiments were repeated at least three times, and a representative experiment is shown. Scale bar = 10 μm.
Article Snippet: We used the following mouse monoclonal antibodies: clone SC-35 against SC35 (Cat# ab11826, Abcam), clone 3F8 against CPSF5 (Cat# H00011051-M12, Novus Biologicals), clone
Techniques: Infection, Staining, Fluorescence, Microscopy, Generated