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Here we outline probe-directed degradation (PDD), a DSN/probe hybridization-based method for depletion of unwanted cDNA sequences from RNA-seq libraries.
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Recently, methods for depletion of brain 5-HT alsoalso neuroimaging studies to assess brain 5-HT level in vivo were applied to migraine.
Methods for depletion of such unwanted sequences typically require treatment of RNA samples prior to library preparation, are costly and not suited to unusual species and applications.
We then depleted the two Sec24 gene products that are both expressed in S2 cells (see DRSC, Drosophila RNAi screening center, http://www.flyrnai.org/) (see 'Materials and methods' for depletion controls).
Given the complexity and wide range of protein concentrations in the plasma/serum proteome, most glycoproteomic workflows have incorporated one of the several available methods for depletion of abundant proteins as the first step in the fractionation of serum or plasma.
Investigation of the practicability and performance of a magnetic micro-particle based method for protein depletion of serum samples, preceding the quantitative analysis of small molecules by LC MS/MS.
Thus Amrolia and colleagues at Baylor College of Medicine, USA and Great Ormond Street Hospital have developed a method for the depletion of allo-reactive T cells from a HSCT before transplantation.
In this study we characterised PDD as an efficient, accurate and flexible method for the depletion of problematic sequences from RNA-seq libraries.
To determine whether macrophages mediate the clearance of senescent cells, we took advantage of an efficient method for macrophage depletion, based on the intravenous administration of selectively toxic, clodronate salt-filled liposomes (clodrosomes).
It was clear that a more specific and more rapid method for the depletion particularly of PtdIns(4,5) P2 was required to investigate the specific roles of each of the phosphoinositides in STIM1 translocation.
Of all the methods employed for depletion, immunoaffinity chromatography is more effective in removing targeted proteins, with minimal carryover, high longevity, minimal nonspecific binding and high reproducibility [ 8, 9].
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