Homework Answers
Inorder to synthesize cDNA from RNA, Reverse Transcription is used. However, RNA strands are susceptible to forming secondary structures such as hairpins, stem-loops and even more complicated structures.The stability of these structures often compromises the synthesis of full-length DNA. To prevent this, we subject RNA to a temperature of 65 degree celsius to denature it. This way, more cDNA can be synthesized from RNA.
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TISL slalu SHLIC33 (CDNA SYU 1. Dilute 1 ug of total template RNA to a final...
you have a solution containing 9 ug/ul of DNA. How would you dilute this to 1...
you have a solution containing 9 ug/ul of DNA. How would you dilute this to 1 ug/ul? make your final volume 0.1 ml
solve for gel preparation and PCR mastermix calculations with steps for understanding TBE Buffer Calculations Determine...
solve for gel preparation and PCR mastermix calculations with
steps for understanding
TBE Buffer Calculations Determine the mass of the following reagents for a 10X stock 700mM of Tris Base (157g/mol) 887mM of Boric Acid (62g/mol) 25.7mM of EDTA (292g/mol) Dissolve in 750ml of DIH.O and bring to volume (IL) Calculate the dilution of your 10x stock for a 1X working stock. Remember you only need IL of working stock for a single experiment. Gel Preparation Calculations You need to...
please , i need Write the protocol by your own words ( steeps) 5. Add 1...
please , i need Write the protocol by your own words (
steeps)
5. Add 1 volume of 70% ethanol to the cleared lysate, and mix immediately by pipetting. Do not centrifuge. Proceed immediately to step 6. Note: The volume of lysate may be less than 350 pl or 600 pl due to loss during homogenization and centrifugation in steps 3 and 4. Note: Precipitates may be visible after addition of ethanol. This does not affect the procedure. 6. Transfer...
En (2 points) You isolated your mitochondrial DNA in Part I. In step 6, you discard...
En (2 points) You isolated your mitochondrial DNA in Part I. In step 6, you discard the supernatant, but keep the pellet. In step 15, you discard the pellet, but keep the supernatant. Explain why the pattern is different between the two steps and the consequence of mixing up these two steps. Procedure Part 1: mt DNA Isolation from your cheek cells. Lysis solution is used to breakdown the cells in this step, you will isolate MEONA from cheek cells....
Pre-Lab Assignment 1) Draw the reaction mechanism for the reaction. 2) Determine the limiting reagent. Procedure...
Pre-Lab Assignment
1) Draw the reaction mechanism for the reaction.
2) Determine the limiting reagent.
Procedure 1 Place approximately 1 g of stilbene dibromide prepared in last week's experiment in a 50 mL round bottom flask. Record the exact mass. Add 0.8 g of KOH and 4 mL of triethylene glycol from the syringe provided in the fume hood (rinse any crystals from the sides of the flask while adding triethylene glycol). 2 Heat the stirred reaction mixture to a...
1. Describe the functions of the following reagents in extraction of DNA from corn meal: proteina...
1. Describe the functions of the following reagents in extraction of DNA from corn meal: proteinase K; guanidine HCI; SDS 2. Why is the ratio of the OD at 260 and 280 nm used to estimate DNA purity? 3. In one paragraph, summarize basic principles of PCR technique in your own words. List all the reagents you will need to perform a PCR experiment. Does this method tell you what genetic modifications were made? If yes, describe how you can...
For the preparation and standardization of NaOH with KHP im supposed to boil water for 1hr and 30 min to remove CO2
For the preparation and standardization of NaOH with KHP im supposed to boil water for 1hr and 30 min to remove CO2....the problem is that if I don't boil it for that long and (30 min) b/c of not enough time but I put the water I boiled for 1/2 hr aproximately into a NaOH bottle with a CO2 absorber and stored it there for a few days. I would assume that I would have to boil the water again...but...
solve for gel preparation and PCR mastermix calculations with
steps for understanding
TBE Buffer Calculations Determine the mass of the following reagents for a 10X stock 700mM of Tris Base (157g/mol) 887mM of Boric Acid (62g/mol) 25.7mM of EDTA (292g/mol) Dissolve in 750ml of DIH.O and bring to volume (IL) Calculate the dilution of your 10x stock for a 1X working stock. Remember you only need IL of working stock for a single experiment. Gel Preparation Calculations You need to...
please , i need Write the protocol by your own words (
steeps)
5. Add 1 volume of 70% ethanol to the cleared lysate, and mix immediately by pipetting. Do not centrifuge. Proceed immediately to step 6. Note: The volume of lysate may be less than 350 pl or 600 pl due to loss during homogenization and centrifugation in steps 3 and 4. Note: Precipitates may be visible after addition of ethanol. This does not affect the procedure. 6. Transfer...
En (2 points) You isolated your mitochondrial DNA in Part I. In step 6, you discard the supernatant, but keep the pellet. In step 15, you discard the pellet, but keep the supernatant. Explain why the pattern is different between the two steps and the consequence of mixing up these two steps. Procedure Part 1: mt DNA Isolation from your cheek cells. Lysis solution is used to breakdown the cells in this step, you will isolate MEONA from cheek cells....
Pre-Lab Assignment
1) Draw the reaction mechanism for the reaction.
2) Determine the limiting reagent.
Procedure 1 Place approximately 1 g of stilbene dibromide prepared in last week's experiment in a 50 mL round bottom flask. Record the exact mass. Add 0.8 g of KOH and 4 mL of triethylene glycol from the syringe provided in the fume hood (rinse any crystals from the sides of the flask while adding triethylene glycol). 2 Heat the stirred reaction mixture to a...
1. Describe the functions of the following reagents in extraction of DNA from corn meal: proteinase K; guanidine HCI; SDS 2. Why is the ratio of the OD at 260 and 280 nm used to estimate DNA purity? 3. In one paragraph, summarize basic principles of PCR technique in your own words. List all the reagents you will need to perform a PCR experiment. Does this method tell you what genetic modifications were made? If yes, describe how you can...
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