Ans 4) We need to wait for the column bed to be 'dry' before adding the protein so that it would not get mix with anything else to prevent it from diffusing in any other substance. There is requirement to add more buffer when protein mixture was loaded in the column to avoid it from drying. So that the molecules cannot pass through it.
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4. Why did you need to wait for the column bed to be "dry" (the absence...
these questions are in reference to gel filtration
chromatography
Fost lab questions on lab 8: Analysis of Laboratory Results 1. If the following mix of molecules were parified using sine exclusion chromatography, what would be the 6 WI onder in which the molecules pass chrough the opening in the bottom of the column? Mixture containingR hemoglobin, 65,000 daltons; myoglobin, 17,000 daltons; myosin, 180,000 daltons. rhe tw First molecule to appear Second molecule to appear Third molecule to appear 2. Ifa...
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SOLUTION MAKING in water. Calculate the amount of NaCl you need to weigh out. 1 (a). You need 500mL of 15% (w/v) NaCl 1(b) What approximate volume of water would you dissolve the NaCl in? Please give a range of volumes. 1(c). Assuming that adding the NaCI to your original volume of water caused the volume to increase by 50mL before you added additional water to reach your final volume, what is the DENSITY of your final...
Molecular Key Calculation - PLEASE NEED
HELP TO CALCULATE IT!
You are setting up you own Master Mix for doing a Not1
restriction digest.
In each digestion tube you will be adding 10 ul DNA and 40 ul of
your Master mix.
You are given 10 x Not1 buffer, 10 ug/ul acetylated BSA, Not1
restiction enzyme 10 units/ul and sterile water.
How much of each of the 4 reagents would you use to make 500 ul of...
Why would one add buffer before removing the comb? Summarize how to first obtain a sample via pipette (specifically an adjustable pipette) and then load into the well Why is it necessary to use a new tip for each well? What factors affect the accuracy of liquid uptake? What is the relevance of the difference between the first and second stop? Have you pipetted before? Are you guilty of banging the pipette to “firmly” attach the tip? What are the...
Before taking this course, did you feel you would benefit from consuming more protein? Why or why not? - Based on your estimate of your current protein intake using you MyDietAnalysis 3 Day report, do you already meet or exceed the suggested protein intake for athletes indicated above? - Using an Internet search, identify at least two adverse effects to people’s health, and two adverse effects on the environment, that could result from increasing the current RDA for protein. How...
kindly answer the 3 questions not more than few sentences.
thank you!!
4. When separating two compounds with boiling points that are very close together, how would adding an extra fractional column (one on top of the other) in the fractional distillation setup affect the purity of the fractions? Why? 5. When distilling a water/ethanol mixture, which of the two compounds predominately distills first? Why? 3. What is an alternative to using boiling chips in a distillation?
1. How did the melting point of your acetanilide change after recrystallization? 2. Why would you test the purity of your acetanilide by mixing it with a known, pure sample of acetanilide and rechecking the m.p.?
You are dissatisfied with the purity of the final preparation of
your HRP and decided to include ion-exchange (IEC) and
gel-exclusion chromatography (GEC) steps in your purification
protocol. From the literature, you found out the following info
about HRP enzyme:
Molecular weight: 40,000
Isoelectric point: 7.2
HRP is a very stable protein.
2: Design GEC purification experiment using the information in
the appendix. Address and justify the following
I. choice of GEC column
II. choice of the buffer (if you...
please help on all questions and explain because i really need
help in this!!! :)
1) After rinsing the buret with water, filling the buret with the solu forgot to do this? the buret with water, why was it rinsed three times with the NaOH solution before uret with the solution? How would this affect your final molarity of NaOH, if you 2) Does the amount of water used to dissolve the KHP affect the molarity of the NaOH solution?...
You find yourself setting up another Western blot, however. today you are preparing the samples to load onto the SDS-PAGE gel. You are using a 4-20%SDS-PAGE gel that can hold a maximum of 30 μしper 1 You remember from you so decided to prepare each sample with a final volume of 25 uL. However, no one is perfect at pipetting, so make sure each sample is made at 1.5X the total volume needed per well. The protein you are interested...