Ppt Template Free _TOP_ Download Biology

Science communications made easy? Look no further. These biology thesis slides have everything you need to spotlight your research and share your results with your thesis committee. Use the ready-made, professionally designed slides for your introduction, research methodology, results, and conclusion. Choose your own color scheme, font combination, and graphics. Easily add charts, graphs, illustrations, and other figures. Experiment with the page animation feature. Check out the handy How-To page at the start of the deck for tips on using these slides as a Google Slides theme, PowerPoint template, or Canva theme.

The IEEE Open Journal of Engineering in Medicine and Biology covers the development and application of engineering concepts and methods to biology, medicine and health sciences to provide effective solutions to biological, medical and healthcare problems.

Ppt Template Free Download Biology

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The template linked above is optimized for the latest June 2022 LaTeX release and may return errors if you are using an older version of LaTeX. Click here to download an older version of the template.

As stated in the PLOS template, your reference information should be included in your .tex file (not submitted separately as .bib or .bbl). Here is a step-by-step way to include your reference list directly within your .tex file:

Authors are encouraged to use the Microsoft Word template or LaTeX template to prepare their manuscript. Using the template file will substantially shorten the time to complete copy-editing and publication of accepted manuscripts. The total amount of data for all files must not exceed 120 MB. If this is a problem, please contact the Editorial Office [email protected]. Accepted file formats are:

Disclaimer: Usage of these templates is exclusively intended for submission to the journal for peer-review, and strictly limited to this purpose and it cannot be used for posting online on preprint servers or other websites.

I finally settled down my Notion workspace and decided to share it as my first template! I am doing my PhD in the multidisciplinary field of structural biology, so I have to keep track of multiple intrinsically different aspects. Hope you find it helpful! I will occasionally improve it, maybe by adding more complex logic or templates for Lab journal section.

You should consider the best way to structure your article before you begin writing. If you wish to use a LaTeX template to format your manuscript (this is optional, you are not obliged to do so) then the files are available in zipped format and Unix tar gzipped format here. Your article should follow the Introduction, Methods, Results and Discussion system, and usually consist of the following sections:

Figures are converted and sized to the journal template as part of the production process for accepted articles, but they are not normally edited further. It is your responsibility to ensure that the figures you supply are legible and technically correct.

Characters should appear as they would be set in the main body of the article. Aim for text sizes of 8 to 12 pt at the final figure size: typically 8.5cm for a small/single-column figure and 15cm for a large/double-column figure. Micrographs should include a scale bar of appropriate size, e.g. 1 m. Figures should be numbered in the order in which they are referred to in the text, using sequential numerals (e.g. figure 1, figure 2, etc.).

New stub templates and categories (collectively "stub types") should not be created without prior proposal at Wikipedia:WikiProject Stub sorting/Proposals. This allows for the proper coordination of all stub types across Wikipedia, and for the checking of any new stub type for possible problems prior to its creation.

A bio for your company website (like on a team or staff page) is where you can opt out of some standard details, such as your title, in favor of things that distinguish you as a pro (or a person). After all, anyone reading this knows where you work and your job title will likely be listed by default. So you can use the second and third paragraph of the template to craft a bio focused on what makes you unique.

If you are submitting an article to Genome Biology, AJE has a helpful tool for authors to get started. The AJE template below is designed to help you with preparing your article for submission. For more detailed information about Genome Biology and its submission guidelines, please go to the journal's official website.

Genome Biology publishes outstanding research in all areas of biology and biomedicine studied from a genomic and post-genomic perspective, and is the highest ranked open access journal in the category.

All learners take in information differently. Note-taking templates can be helpful tools for organizing your learning. Within this section, you will be introduced to three styles of note-taking templates.

Cell biology illustrations and templates that are optimized for scientific publications, presentations and posters. Downloads include cellular backgrounds in a variety of colors with and without lipid membranes, nuclei, golgi, blood vessels, DNA strands, epithelial cell layers, and other cell background illustrations.

We present a novel modular, stochastic model for biological template-based linear chain elongation processes. In this model, elongation complexes (ECs; DNA polymerase, RNA polymerase, or ribosomes associated with nascent chains) that span a finite number of template units step along the template, one after another, with semaphore constructs preventing overtaking. The central elongation module is readily extended with modules that represent initiation and termination processes. The model was used to explore the effect of EC span on motor velocity and dispersion, and the effect of initiation activator and repressor binding kinetics on the overall elongation dynamics. The results demonstrate that (1) motors that move smoothly are able to travel at a greater velocity and closer together than motors that move more erratically, and (2) the rate at which completed chains are released is proportional to the occupancy or vacancy of activator or repressor binding sites only when initiation or activator/repressor dissociation is slow in comparison with elongation.

The CRISPR-Cas9 system is a powerful genome-editing tool in which a guide RNA targets Cas9 to a site in the genome, where the Cas9 nuclease then induces a double-stranded break (DSB). The potential of CRISPR-Cas9 to deliver precise genome editing is hindered by the low efficiency of homology-directed repair (HDR), which is required to incorporate a donor DNA template encoding desired genome edits near the DSB. We present a strategy to enhance HDR efficiency by covalently tethering a single-stranded oligodeoxynucleotide (ssODN) to the Cas9-guide RNA ribonucleoprotein (RNP) complex via a fused HUH endonuclease, thus spatially and temporally co-localizing the DSB machinery and donor DNA. We demonstrate up to a 30-fold enhancement of HDR using several editing assays, including repair of a frameshift and in-frame insertions of protein tags. The improved HDR efficiency is observed in multiple cell types and target loci and is more pronounced at low RNP concentrations.

We reasoned that a strategy to covalently tether the DNA donor template to the Cas9-guide RNA ribonucleoprotein (RNP) could dramatically enhance HDR efficiency by guaranteeing the presence of the donor DNA at the site of the DSB with the RNP complex, thus increasing the effective concentration of the donor template at the DSB and reducing the dimensionality of the reaction. In a recently described method termed S1mplex11, authors used recombinant streptavidin to bridge a modified single-guide RNA (sgRNA) containing a streptavidin-binding aptamer and a biotinylated single-stranded oligodeoxynucleotide (ssODN) to deliver a linked RNP-donor DNA complex and observed enhancement in precise genome editing compared to unlinked components. However, this method, along with other recent attempts to co-deliver the donor DNA using biotin-avidin12 and the SNAP tag13, requires additional steps and expense associated with modifying the donor DNA and inclusion of additional recombinant proteins. Additionally, the S1mplex method generally suffers from decreased absolute HDR rates11.

We recently showed that HUH endonucleases form robust covalent bonds with specific sequences of unmodified single-stranded DNA (ssDNA) and can function in fusion tags with diverse protein partners, including Cas914. Formation of a phosphotyrosine bond between ssDNA and HUH endonucleases occurs within minutes at room temperature. Tethering the donor DNA template to Cas9 utilizing an HUH endonuclease could thus be a powerful approach to create a stable covalent RNP-ssODN complex without the need for chemical modification of the ssODN, alteration of the sgRNA, or additional proteins. We demonstrate that covalent-tethering of an ssODN via HUH-Cas9 fusion proteins results in up to a 30-fold enhancement of HDR. We present relative and absolute readouts of HDR using several editing assays, including repair of a frameshift and in-frame insertions of protein tags. The improved HDR efficiency is observed in multiple cell types and target loci and is more pronounced at low RNP concentrations.

Selective covalent attachment of ssDNA to Cas9-PCV. a Schematic of Cas9 fused to the HUH endonuclease PCV with a covalently attached ssODN. b SDS-PAGE of Cas9 variants reacted with an Alexa 488 fluorescently labeled ssDNA containing the PCV recognition sequence. The top panel is the coomassie stained gel, and the bottom panel is the identical fluorescently imaged gel. PCV is fused to either the carboxyl (Cas9-PCV) or amino (PCV-Cas9) terminus of Cas9. Cas9-PCV (Y96F) represents catalytically inactive PCV (Y96F) fused to Cas9. c SDS-PAGE gel shift assay of Cas9 reacting with two ssDNA templates containing the PCV recognition sequence of differing lengths in a 1:1 ssDNA:Cas9 molar ratio e24fc04721