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文献和实验Isolation of an mRNA-Binding Protein Involved in C-to-U Editing
with high affinity. Here we outline a protocol for purifying Apobec-1 complementation factor (ACF), the RNA-binding subunit of the apolipoprotein-B (apo-B) mRNA-editing enzyme. ACF was purified using synthetic wild-type and mutant apo-B RNAs
Mouse and Other Rodent Models of C to U RNA Editing
-1 and a requisite cofactor, apobec-1 complementation factor (ACF). The underlying biochemical and genetic mechanisms regulating tissue-specific apoB mRNA editing have been accelerated through development and characterization of physiological rodent models
In Situ Proximity Ligation Assay for Microscopy and Flow Cytometry
proximity probes targeting a mouse monoclonal anti‐HER2 antibody and a rabbit polyclonal anti‐HER2 antibody. Cell nuclei were counterstained with Hoechst dye (blue). View Image
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