Concentration =
Absorbanve/Pathlength×Conversion factor×Dilution factor
= 0.025/1 *50 ng/ul* 200 = 250 ng/ul
Original DNA sample has 250 ng/ul and we need only 25ng hence we can dilute 1:10 ratio and use 1 ul of diluted sample that contains 25ng/ul for sequencing
It is common to use 25 ng of DNA for a sequencing reaction. You have a...
You have prepared some plasmid DNA in lab and need to know its concentration so you can load 1 ug on a gel. You dilute 1 uL with 99 uL of water and the resulting sample has an absorbance of 0.075. What volume of the original sample do you need to load onto the gel? (Show math for partial credit and make sure you are answering the question I am actually asking.)
Short Answer (2 pts) (partial credit allowed) 3. When making a genomic DNA library, it is common to start with 10 ug of genomic DNA. Your liver preparation was diluted (luL with 249 uL of water) and the absorbance of the diluted sample at 260 nm was 0.035. How much of the undiluted sample will you need to use to make the library? (Show math for partial credit)
When would you want to use Shotgun Sequencing? a. Whenever both strands of the DNA are being sequenced in the same reaction tube(s). b. When radioactive nucleotides are to be used to terminate replication. c. When a large piece of DNA (like a genome) needs to be sequenced. d. Whenever the DNA sequence is unknown.
LAB DATA The lab data shown below reflects what you would have collected during lab on campus. Use this "virtual lab data" to complete the calculations in this lab. Concentration (M) of starting solution .024 1st Reading 2nd Reading Abs (15-mL .024 M Cu2+ + 7 mL conc NH, diluted with distilled H 0 to 100 mL total volume) 0.945 0.923 Abs (5-mL .024 M Cu2+ + 7 mL conc NH, diluted with distilled H,0 to 100 mL total volume)...
You have a DNA sample (liquid) with concentration 67.5 nanograms/microliter. You want to dilute it to a final concentration of 25 nanograms/microliter. How do you accomplish this? (note: you can use a final volume such as 200 microliters)
2. (you don't Show using Hess's Law how the enthalpy of reaction for HCL + NaOH need specific numbers, just call it AH) minus the enthalpy of reaction for HCheg) + NH ) (call it AH.) should be equal to the enthalpy of reaction for NaOH2 + NH Cla). Show all work. with a concentration of 0.160 M has an absorbance of 0.80 in a 1.0 cm path length cuvette. (a) What would be the absorbance expected if the sample...
BELOW I ATTACHED A OVERVIEW OF FORMULAS SHOW ALL WORK IN DETAIL. NEED ANSWERS ASAP Concentration (M) of starting solution .024 1st Reading 2nd Reading Abs (15-mL .024 M Cu2+ + 7 mL conc NH3 diluted with distilled H2O to 100 mL total volume) 0.861 0.941 Abs (5-mL .024 M Cu2+ + 7 mL conc NH3 diluted with distilled H2O to 100 mL total volume) 0.541 0.518 Abs (15-mL Unknown Cu2+ solution + 7 mL conc NHz diluted with distilled...
A Bradford assay was carried out to measure protein concentration. The absorbance of five standard samples and two unknown samples are listed in the table below. The Bradford reaction mixture (1 ml) was prepared as follows: 100 μl sample A or sample B + 200 μl Bradford reagent + 700μl 0.9% NaCl solution sample ID concentration (mM) absorbance (O.D.) std 1 100 0.78 std 2 50 0.4 std 3 25 0.18 std 4 12.5 0.08 std 5 0 0 ...
1. You have generated the following standard curve after a Bradford Assay to measure Absorbance vs samples of known BSA concentrations. Now you need to determine the amount of protein in two mitochondria samples taken from fish, one taken from fish under normal conditions and the other taken from fish under oxidative stress. The absorbance reading for the normal fish fraction was A595=175, and the absorbance reading for the stressed fish fraction was A595= 275 Bradford Assay Standard Curve y...
A. You have been given a tube of E. coli. You are asked to make 1 mL total volume of 10-1 dilution of the bacterial culture. Explain how you would do this. Show all necessary calculations. ____ ml cells + _____ ml water = 1 ml (total volume) B. Next, you were asked to make a 10-2 dilution of the bacterial sample. Explain how you would perform this. Show all necessary calculations. You have bacteria at a concentration of 2...