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We narrowed to 960 results for: comp

Showing: 241 - 250 of 960 results
  1. What Do I Do Now? Academic v. Non-Academic Career Decisions

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    Blog Post
    ...Table 1: Taking it a Step Further - Big Company v. Small Company Big (e.g. Pharma) Small (e.g. Biotech...advancement in one company, good performers in for the long haul Limited movement in one company, likely will...academic silo to tenured professor.  Non-academia encompasses millions of choices including pharma, tech transfer...options in nonprofit science. No one list can ever encompass them all. We can’t designate non-academic jobs...and teach students Collaborations may be less “complicated” - for example, easy to initiate a collaboration...More sources of training and resources within the company Must find own sources of knowledge often externally...every 3-6 years—a short and exciting ride Complicated matrix structures are common Small integrated...
  2. Technical Design of a Western Blot

    Type
    Blog Post
    ...protein. Proteins located in membrane-bound subcompartments, like the mitochondria or nucleus, will likely...loading buffers, as most Bradford assays are not compatible with detergents like SDS, while BCA assays are...their differing chemistries. You therefore cannot compare Bis and Tris gels or blots to each other. Once ...protein-based blocker is either degraded or not completely mixed together.   Commercially available chemical-based...lower cost, and smaller size. However, HRP is not compatible with sodium azide, a common microbial agent used...phosphates have a linear reaction rate and are compatible with antimicrobial agents. Chemiluminescence ...chemiluminescence enzymes, they are more likely to be compatible with stripping and probing.   Imaging At the ...
  3. Flow Cytometry Readouts: Yes, No, and Everything in Between

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    Blog Post
    ...easier to identify by comparing peak positions to the base expression. When compared to the control — which... voltage has been adjusted appropriately and compensation performed. Before you read out your plots, you...to make sure you’ve also adjusted voltage and compensated your colors. Here are some good practice tips...population cluster would be shifted to the right in comparison, say somewhere between a 104–105 signal intensity...place your gate based on the dot plot would be complicated.  Figure 2: (A) a smeary dot plot showing...with the baseline suggesting this sample has a comparable expression to the baseline/negative control. ... populations in the histogram plot in Figure 4 compared to the dot plot in Figure 2. Quantification using...
  4. Antibodies 101: ChIP

    Type
    Blog Post
    ...protein:DNA complexes with antibodies specific to your protein(s) of interest. Once the complex is captured...protein:DNA complexes and finally (5) isolated the DNA from your antibody:protein:DNA complexes. Your DNA... the first step is to ensure your protein:DNA complexes will remain bound to each other until you are ...reversible bonds. This will keep the protein:DNA complexes together until you want to break them. Crosslinking...digestion can preserve more of the protein:DNA complexes. Once you’ve finished fragmenting the DNA, spin...that?  So while this method is certainly long and complex, you may be thinking, well, these are mostly fairly...techniques. What’s all the fuss? Well, ChIP’s complexities come not from the techniques used, but from ...
  5. 7 Tips to Secure a STEAM Internship This Summer

    Type
    Blog Post
    ...that the classroom cannot offer. Furthermore, companies across most industries tend to hire their former...Prior to March 2020, internships were a fiercely competitive endeavor. Due to the COVID-19 pandemic, students...college, and graduate students. In order to gain a competitive advantage this cycle, consider the advice below...which is the perfect opportunity to paint a comprehensive picture of your academic interests, potential... impress the judges on your ability to tell a compelling narrative that is positive, and forward-looking...counterintuitive since that approach seems to create competition for your own spot. True! But you create a network...sense approaches that will prepare you for the competitive landscape beyond college. They will also serve...
  6. A Quick Guide to a Career in Software Product Management

    Type
    Blog Post
    ...career at a biotech company, I always assumed I’d work one or two years at the company and then go to grad... the head of software product management at my company was open to meeting with me and explaining more...software product manager helps ensure that the company or software group is building the software tools...Well, I’ll give you an example. At my previous company, Ginkgo Bioworks, our software development team...backgrounds, most did not. It was my job to translate complex lab operations workflows into a format the developers... to solve is clear, but the solution is more complicated. You’ll need to be creative to be able to work...framework If you can’t find internships at science companies, try to find internships with translatable skills...
  7. Advice on Career Paths and the Green Card Process for International Researchers and Entrepreneurs

    Type
    Blog Post
    ...requirement if you work for a private company you must show that your company employs at least 3 full-time people...Within these sectors, you could start your own company, work in a bench research career or a non-bench... to find the perfect job immediately after you complete your Ph.D. or postdoc. Foreign national researchers... need to be aware of the April 1 deadline for companies to submit an application on their behalf.  If ...technology transfer, communications, medical writing, compliance, core facility management, collaboration management...be directed to you specifically. You must also complete the peer review for it to be counted as proof ...your CV and bio sketch whenever you have new accomplishments to add. Obtain copies and translations of documents...
  8. Easi-CRISPR: Generating Knock-In and Conditional Mouse Models

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    Blog Post
    ...challenging for sequences with complex secondary structure. Today, multiple companies offer long single-stranded...ribonucleoprotein (RNP) complexes of Cas9 protein and the separated guide RNA components (crRNA and tracrRNA...months. With CRISPR (B), you can inject CRISPR components directly into a zygote and obtain a knockout ...maximum Easi-CRISPR efficiency. Easi-CRISPR is compatible with standard microinjection and electroporation...successfully used guides targeting the same or complementary strands, as well as guides facing towards or... simple method for delivery of genome editing components to the germline. In contrast to standard microinjection...placed to mediate electroporation. Ohtsuka et al. compared traditional microinjection and i-GONAD knock-in...
  9. Generating Mouse Models Using CRISPR/Cas9

    Type
    Blog Post
    ...engineered ESCs), and chimeric adults mated to produce completely transgenic offspring. Although powerful, this... genome, the CRISPR/Cas system makes use of 3 components, a guide RNA (gRNA) of about 125 nt that specifies...gRNA, Cas9, and donor oligonucleotide or plasmid components are brought together and microinjected into either...eggs. Or, to avoid handling embryos ex vivo, the components can be electroporated into the oviduct of pregnant... major advantages of CRISPR mouse editing when compared to more conventional methods. First, one can work... work with almost any strains of mice, as compared with conventional gene targeting, which is limited ...including 129 and C57BL/6, for which we have germline competent ESC lines. Second, the process is much quicker...
  10. Plasmids 101: In-house NGS Plasmid Quality Control Now at Addgene

    Type
    Blog Post
    ...MiSeq that takes about two days to complete. After the run completes, we begin our assembly process. Again...sufficient quantity for sequencing. This process is completed in a plate format yielding anywhere from two to...Illumina sequencing on our newly donated MiSeq.  For Complete Plasmid Sequencing we perform a 2x251 run on our...annotated Genbank files that are useful for more complicated plasmids, like those that contain synthesized...mutations, truncations, and insertions that could compromise function. When we do find mutations, we check..., NGS for some plasmids will not result in one complete, circular assembly. Most of the time, these plasmids...obtain an NGS result that is useful, but not 100% complete, we will still make this data available as a partial...
Showing: 241 - 250 of 960 results