ANOVA assignment

Question: 1. Enumerate the different application of Dyna Bead Analysis. 2. Discuss the significance of this method.

Article - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501646/ Here are the articles provided within the question - They are not needed but are available if additional information is warranted - The figures being mentioned are already provided. This is Biochemoistry, please answer each part to the best of your ability. There are a max of 3 parts due to guidelines and please answer each part with clear and efficient work with answers. Thank you

Please don't provide handwritten solution ......

JUST PROVIDE A BRIEF ANSWER. PLEASE HELPE OUT, I'M BEGGING YOU PLEASE. THANK YOU SO MUCH IN ADVANCE.

Under what conditions, a higher rate in the presence of the inhibitor observed? (how could the effect of inhibitor be compensated) explain

Please help me answer this reviewer. Determine what the statement is describing. Fill in the blanks with the correct/best answer. 1. A fermentation method used by several industries like the pharmaceuticals, food, textile etc., to produce metabolites of microorganisms using solid support in place of the liquid medium. answer: 2: Whole fish whose DNA has been purposefully altered by directly integrating (or deleting) one or several genes to introduce or modify a targeted character.  answer: 3. The process of transferring genetic materials into a living cell using glass micropipettes or metal microinjection needles.  answer: 4. Preservation of components of biological diversity outside their natural habitats. Thank you very much for your help

can you please help me with this? Thank you.

Correct the answer

explain this result in a brief and clear way, Here is the link where the image came from: https://mdpi-res.com/d_attachment/ijms/ijms-21-05129/article_deploy/ijms-21-05129.pdf?version=1595262192

How we can Treatment Thalassemia by using gene therapy? Please answer at your own words,please..

ANSWER THE FOLLOWING

Hello, please read the attached Microbiology question and answer the question correctly. Please aim for about 3-4 sentences max (enough to fit within the lines given). Write in complete sentences (No Bullet Points).  *If you correctly answer the question, I will provide a Thumbs Up to you. Thank you.

Please answer question as best as possible. The identified organism is E. coli . Thank you

Please help me answer and explain these questions: 1. Humans also express serum albumin. How do the predicted molar extinction coefficient and molecular mass of human and bovine serum albumin compare? 2. Which assay (A280 or Bradford) can sense lower concentrations of protein? What is the LOD for each assay?

First page is reference for number 4-7

a. L. What are the possible secondary structures of a primer and what are their effects? Explain with illustrations. 3 I. Why is annealing temperature important and how is it connected to melting termperature? Explain 2 b. Compare and Contrast between (3+2) 1. Progressive and Iterative Alignment 2 Profile, Fingerprint, and HMM Note: Just describing or listing characteristics would disquality the answer. liguion thre

Case Study: You are asked to inoculate lactose media (broth) with E. coli that was growing exponentially in glucose media (broth). You monitor the growth of these cells in the lactose broth using a viable plate count technique and plot the Growth Curve for E. coli growing c lactose. After a day of monitoring the cells, you note that the culture entered into lag phase growth initially and is now currently growing exponentially. In addition, you find that the cultures doubling time is 30 minutes. You know that the doubling time of E. coli in glucose media is 20 minutes. You did not change the oxygen content or temperature at Which you were growing the cells, E. coli is still aerobically respiring at 37°C. Question: If the lac operon is 'on' what does this imply about the cell? O The cell is dying and the lac operon is going to induce apoptosis. Apoptosis is truly cell death and the cells will enter into the death phase of the Growth Curve. O Lactose is being catabolized and glucose is no…

Case Study: You are asked to inoculate lactose media (broth) with E. coli that was growing exponentially in glucose media (broth). You monitor the growth of these cells in the lactose broth using a viable plate count technique and plot the Growth Curve for E. coli growing on lactose. After a day of monitoring the cells, you note that the culture entered into lag phase growth initially and is now currently growing exponentially. In addition, you find that the cultures doubling time is 30 minutes. You know that the doubling time of E. coli in glucose media is 20 minutes. You did not change the oxygen content or temperature at which you were growing the cells, E. coli is still aerobically respiring at 37°C. Question: In order to determine the doubling time of E. coli a viable plate countris performed. This means that you are truly counting O Dead cells only via a microscopic count O Live cells only via membrane filtration or serial dilution O All cells via membrane filtration or serial…

Case Study: You are asked to inoculate lactose media (broth) with E. coli that was growing exponentially in glucose media (broth). You monitor the growth of these cells in the lactose broth using a viable plate count technique and plot the Growth Curve for E. coli growing on lactose. After a day of monitoring the cells, you note that the culture entered into lag phase growth initially and is now currently growing exponentially. In addition, you find that the cultures doubling time is 30 minutes. You know that the doubling time of E. coli in glucose media is 20 minutes. You did not change the oxygen content or temperature at which you were growing the cells, E. coli is still aerobically respiring at 37°C. Question: If you want to grow E. coli as quick as possible would you grow it on lactose or glucose? O Mixing the two carbon sources would provide the most optimal growth conditions. O Lactose because of the generation time being faster. O Lactose and an anaerobic environment. O Glucose…

Discuss about the reagents used for agarose gel electrophoresis (not Polyacrylamide gel electrophoresis)

General Biology - Help me do this activity, you can read the instructions for clarification, thanks!

please answer the 2 question given and include in-text citations and references

General Biology - True or False , you can read the instructions for clarification, thanks!

Calculation for a neutral red assay please include steps since it is essential for the report and it is marked.

וןווד ← Q Lab Report 6 worksheets 314 F22 .DOCX File Edit View Insert Format Tools Help A 100% ¿ Summary Grades for Arysta Visser: 23 x M Uh-oh! There's a problem w X b The restriction EcoRI cleaves X + Untitled spreadsheet - Goog X https://docs.google.com/document/d/1mKY1HIgMPRh1kRDCmX7msBF2yf07-ogT/edit Outline Headings you add to the document will appear here. Normal text Times ... 12 + B I U 2 18. The restriction EcoRI cleaves double-stranded DNA at the sequence 5'-GAATTC-3', the restriction enzyme HindIII cleaves at the sequence 5'-AAGCTT-3', and the restriction enzyme BamHI cleaves at 5'GGATCC-3. An 805 bp circular plasmid is digested with each enzyme individually and then in combination, and the resulting fragment sizes are determined by means of electrophoresis. The results are as follows: 1 Restriction Enzyme(s) EcoRI BamHI HindIII EcoRI and BamHI EcoRI and HindIII BamHI and HindIII 3 Practice ====•=•€ EX Fragment lengths (base pairs) 430 bp, 375 bp 470 bp, 335 bp Lab Report 6…

please answer question b also. b. For the Covid-19 pandemic), give any issues, benefits, or drawbacks of the application (still using three sentences)

Please read these results and explain them briefly in a way that is understood https://mdpi-res.com/d_attachment/ijms/ijms-21-05129/article_deploy/ijms-21-05129.pdf?version=1595262192

Factors which can influence antibiotic susceptibility testing (size of zone inhibition) are_________________.