For the bacterial transformation lab, what was the purpose of mixing calcium chloride solution with bacteria,...
For the bacterial transformation lab, what was the purpose of mixing calcium chloride solution with bacteria, and later performing a heat shock step after you've allowed the bacteria to sit on ice?
Homework Answers
Calcium chloride help in binding of exogenous dna to bacterial cell as it resist repulsion between them.
Then we give high temperature for creating small pore in bacterial membrane and then give ice cold condition for healing of this membranes.
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For the bacterial transformation lab, what was the purpose of
mixing calcium chloride solution with bacteria,...
gene transfer like conjugatione 5. What is calcium chloride transformation? What does it accomplish? Calcium Chloride...
gene transfer like conjugatione 5. What is calcium chloride transformation? What does it accomplish? Calcium Chloride trensformation increases the ability of a bacteria call to in corporale plasmid DNA which callows it to be genetically frensformed. If accomplishes binding op plasmid DNA IV. 6. Why would you expect to find cell growth on the Luria nutrient agar plate? (LB plate)? 7. Did you expect to find cell growth on the ampicillin Luria plate? Explain WHY or WHY NOT. (LB/amp plate...
You are doing a bacterial transformation in Professor Carrico’s Genetics lab. As you are getting ready,...
You are doing a bacterial transformation in Professor Carrico’s Genetics lab. As you are getting ready, you realize that you are out of a critical solution, Calcium Chloride. You look at the bottle and find the Molecular Weight CaCl2 is listed as 110.98g/mol. You need 10 ml of a 2 molar solution. Briefly describe how you would proceed to make this solution.
please help QUESTION 1 When transforming bacterial cells, a researcher is interested in generating bacteria that...
please help
QUESTION 1 When transforming bacterial cells, a researcher is interested in generating bacteria that exogenously express the gene that encodes GFP (green fluorescent protein). After transformation, she finds that no bacteria colonies grew on her selective media. Which of the following best explains the results of her transformation protocol? The concentration of the antibiotics in the selection media was too low, therefore no bacteria grew. Her bacterial cells were not competent so they took up excessive amounts of...
Suppose that you carried out a Bacterial transformation of E. coli HA101 with pGLO plasmid experiment...
Suppose that you carried out a Bacterial transformation of E. coli HA101 with pGLO plasmid experiment in the lab. During the experiment plates with bacteria were inoculated from +GLO and -GLO microfuge tubes (LB (-) plate, LB/amp (-) plate, LB/amp (+) plate, and LB/amp/ara (+) plate). 14) Explain what kinds of bacterial growth you will find on each of 4 plates after incubation ((LB (-) plate, LB/amp (-) plate, LB/amp (+) plate, and LB/amp/ara (+) plate): under normal light and...
Wullugard to GFP and bla, what are the genotypes of E. coli before and after transformation?...
Wullugard to GFP and bla, what are the genotypes of E. coli before and after transformation? 2. What was the purpose of transferring the +DNA and DNA tube from ice to hot water to ice? 3. Why were the tubes incubated at room temperature for 10 minutes before spreading their contents onto the agar plates? Why not just inoculate the plates right after the heat shock?
1. Fill in the table above with what you observe on your plates. 2. Bacterial transformation...
1. Fill in the table above with what you observe on your
plates.
2. Bacterial transformation occurred on which agar plate (s)?
What evidence do you have that the bacteria were transformed
here?
3. Which plates have glowing growth? Explain what causes
bacteria to glow.
II. Transformation of E. coli with Plasmid DNA (PGLO) 1. Three LB (Luria Broth) agar plates are obtained. The plates contain: • Plate A: LB-Agar/Ampicillin/Arabinose • Plate B: LB-Agar/Ampicillin • Plate C: LB-Agar 2. Three...
LAB Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to...
LAB Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...
LAB17 Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to...
LAB17 Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...
Lab Report-Carbohydrates 1. Purpose 2. Special Media for Isolating Bacteria (Lab #12) a. Why are dyes...
Lab Report-Carbohydrates 1. Purpose 2. Special Media for Isolating Bacteria (Lab #12) a. Why are dyes such as phenol red, eosin or methylene blue added to the media? b. How does the bacterium change the media (i.e color of agar or colonies) after incubation? C. In this experiment, which media are selective, and which are differential? d. How did the results observe on the mannitol salt agar and EMB agar correlate to the Gram reaction of the bacteria? e. What...
Question 1 1 pts What is the purpose of utilizing brine (saturated sodium chloride solution) during...
Question 1 1 pts What is the purpose of utilizing brine (saturated sodium chloride solution) during the liquid-liquid extraction portion of the bromohydrination of cyclohexene? To lower the solubility of organic molecules in the organic layer. To stabilize the carbocation formed during the course of the reactions. To remove excess water from the organic layer of the reaction. To ensure that enough water is present for the reaction to generate an alcohol. Question 2 1 pts Which of the following...
gene transfer like conjugatione 5. What is calcium chloride transformation? What does it accomplish? Calcium Chloride trensformation increases the ability of a bacteria call to in corporale plasmid DNA which callows it to be genetically frensformed. If accomplishes binding op plasmid DNA IV. 6. Why would you expect to find cell growth on the Luria nutrient agar plate? (LB plate)? 7. Did you expect to find cell growth on the ampicillin Luria plate? Explain WHY or WHY NOT. (LB/amp plate...
please help
QUESTION 1 When transforming bacterial cells, a researcher is interested in generating bacteria that exogenously express the gene that encodes GFP (green fluorescent protein). After transformation, she finds that no bacteria colonies grew on her selective media. Which of the following best explains the results of her transformation protocol? The concentration of the antibiotics in the selection media was too low, therefore no bacteria grew. Her bacterial cells were not competent so they took up excessive amounts of...
Wullugard to GFP and bla, what are the genotypes of E. coli before and after transformation? 2. What was the purpose of transferring the +DNA and DNA tube from ice to hot water to ice? 3. Why were the tubes incubated at room temperature for 10 minutes before spreading their contents onto the agar plates? Why not just inoculate the plates right after the heat shock?
1. Fill in the table above with what you observe on your
plates.
2. Bacterial transformation occurred on which agar plate (s)?
What evidence do you have that the bacteria were transformed
here?
3. Which plates have glowing growth? Explain what causes
bacteria to glow.
II. Transformation of E. coli with Plasmid DNA (PGLO) 1. Three LB (Luria Broth) agar plates are obtained. The plates contain: • Plate A: LB-Agar/Ampicillin/Arabinose • Plate B: LB-Agar/Ampicillin • Plate C: LB-Agar 2. Three...
LAB Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...
LAB17 Genetic Engineering of Bacteria Problem Is it possible to transfer the allele for resistance to the antibiotic ampicillin into a bacterial cell? Objectives After completing this lab, the student will be able to: 1. Demonstrate micropipetting and sterile pipetting techniques for handling and transferring bacteria and plasmid DNA. 2. Maintain sterile conditions for culturing bacterial cells. 3. Inoculate bacteria into flasks, culture tubes, or agar plates. 4. Culture isolated individual colonies from an agar plate to form genetically identical...
Lab Report-Carbohydrates 1. Purpose 2. Special Media for Isolating Bacteria (Lab #12) a. Why are dyes such as phenol red, eosin or methylene blue added to the media? b. How does the bacterium change the media (i.e color of agar or colonies) after incubation? C. In this experiment, which media are selective, and which are differential? d. How did the results observe on the mannitol salt agar and EMB agar correlate to the Gram reaction of the bacteria? e. What...
Question 1 1 pts What is the purpose of utilizing brine (saturated sodium chloride solution) during the liquid-liquid extraction portion of the bromohydrination of cyclohexene? To lower the solubility of organic molecules in the organic layer. To stabilize the carbocation formed during the course of the reactions. To remove excess water from the organic layer of the reaction. To ensure that enough water is present for the reaction to generate an alcohol. Question 2 1 pts Which of the following...
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