Results
.docx
keyboard_arrow_up
School
Lindenwood University *
*We aren’t endorsed by this school
Course
100
Subject
Biology
Date
Dec 6, 2023
Type
docx
Pages
1
Uploaded by BrigadierWombat3977
Layla Massey & Levi Jeffers
Dr. Welsh
Intro to Cellular and Molecular Bio
21 September 2023
Results
Starting with our CFU counts LB gave us CFU/ml=820000 in our serial dilution batch of
-3. For CFU of BHI we had CFU/ml=3*10^8 in our serial dilution batch of -6. We were able to
come out with two master plates of LB which is 48 colonies and the same amount for BHI. We
had some that were yellow, white, creamy, and we also had a strange one that was red. We tested
our masterplates against Bacillus subtilis and Escherichia coli. We had 4 colonies that were able
to come out with a positive halo around them against the Bacillus subtilis, we were unlucky and
didn't have any that tested against Escherichia coli. All of our colonies that tested positive were
bacteria that was grown on the LB agar. Sections 12 and 16 from LB 1 which is our first section
of the two master plates both had amazing growth when we did our streak plates for them.
Section 1 and 2 from LB 2 had a couple complications when we did the streak plates. so we had
to redo section 1 because it had no growth on it the first time but then it had amazing
growth the second time. Sections 16 and 1 both had a yellow tone to them while sections
12 and 2 had more of a white creamy tone to them. Also, section 1 changed color from master
plates to streak plates from yellow tone, to more brown. We then used these for sections for a
gram stain which if the stain is pink it is gram negative and if it is purple it is gram positive.
Sections 16, 12, and 1 were all gram negative when we looked at them under the microscope. We
were lucky enough to have section 2 which came out gram positive.
No screening
Screening for B-sub
Screening for E-coli
Master Plates LB
48 bacteria isolates
4 bacteria isolates
0 bacteria isolates
Master Plates BHI
48 bacteria isolates
0 bacteria isolates
0 bacteria isolates
Table 1-Master Plate isolates and their antibiotic production
Figure 1
Figure 2
Figure 1:streak plate of LB 2 section 1
Figure 2:gram stain of LB 2 section 1
Discover more documents: Sign up today!
Unlock a world of knowledge! Explore tailored content for a richer learning experience. Here's what you'll get:
- Access to all documents
- Unlimited textbook solutions
- 24/7 expert homework help
Related Questions
Hi, hope you're doing great!
I need help with a question, I have screenshot
thank you!
arrow_forward
please solve this step by step calculations
arrow_forward
Please help me ??? very urgently need to submit and the question is complete please help ASAP will appreciate your help?
arrow_forward
Theoretical Data
Following the modified protocol for the isolation of Escherichia coli bacteriophage of Encabo (2018)
presented below, compute for the pfu/ml of the chloroform-treated lysate.
1ml
1ml
1ml 1ml
1
Chloroform-treated lysate
1ml
Dilution
10-3
10-4
10-5
0 0 0 0 0
9ml
9ml 9ml
10-1
10-²
10-3
Empty sterile
tubes
Incubate inside ref for 15-20min
+ 0.1 ml lysate-E.coli mix
0.1 ml
9ml 9ml
104
10.5
//
0.1 ml
0.1 ml
+0.5 ml E. coli
↓↓↓↓↓↓
Incubate O/N at 35°C,
observe for plaques
Molten soft agar
overlay
B. Quantification of the Infective E. coli other Bacteriophage Particles in the Raw Sewage
Sample
Volume of Stock Plated (in ml)
Bottom agar
No. of Plaque-Forming Units (pfu)
Ave.
A
B
254
265
132
110
11
23
arrow_forward
I am not understanding why TA of alcohol precipitation is used as TA of purified protein. I provided 2 photos, 1 with the questions and the correct answer, and the other photo is a screenshot of the explanation.
arrow_forward
Asap
arrow_forward
D
Question 9
An enzyme assay of 2 mL of extract shows 7.3 U/mL and a biuret assay shows 4
mg/mL protein on the initial sample. It is salted out and the pellet is washed and
resuspended in 0.4 mL buffer. It is re-assayed and shows 12.1 U/mL activity and
1.3 mg/mL protein. What is the change in fold purity for this sample? (answer to
2 decimal places)
arrow_forward
Calculate these for 1 ug of plasmid DNA in a final total volume of 20 ul. All
enzymes being used here are at a concentration of 10 U/µL. For double digests, give the
appropriate volume for each enzyme and decide which buffer to use. (HINT: look up double
digest conditions on the NEB website.) You should always calculate all volumes in advance to
ensure the correct working concentrations and so that you can prepare the digests as efficiently
as possible. It is a good idea to check off each component as it is added to the microfuge tube.
Complete the table below, including the volume of DNA sample(s) you will need for 1 pg of the
DNA (from two different methods in Experiment #3) based on the concentration(s) you
determined from the OD260 value, which you will restriction digest with each of the restriction
enzymes singly and in double digests in Part A.
For example, the volume of DNA sample that contains 1 µg DNA for DNA sample from Part A,
Experiment 3: OD260 = 0.024, dilution 500x…
arrow_forward
d/e/1FAIpQLSfTle9UfP15_VUqFI-ACEQd1XBykXv5Lr4dEMQbLJ1d6fCupw/viewform
Students subjected three samples of five different molecules to gel electrophoresis
as shown in Figure 1
A B
C DE
+2
3
Wells
4
8. Which of the following statements best explains the pattern seen on the *
gel with regard to the size and charge of molecules A and B?
1 point
molecules A and B are positively charged, and molecule A is smaller than molecule
B.
molecules A and B are positively charged, and molecule A is larger than molecule B.
molecules A and B are negatively charged, and molecule A is smaller than molecule
B.
molecules A and B are negatively charged, and molecule A is larger than molecule B.
Sign out
arrow_forward
None
arrow_forward
bio 111 intro to cell, i need help in my post lab assignment. read the question carefully please and if you have any questions
arrow_forward
Hello. Please see the attached screenshot. Please demonstrate how the entropy score was calculated. Thank you.
arrow_forward
WELL NUMBER
ORGANISM
1
2
3
4
6
7
8
Human
+++
+++
+ tt
t++
+ ++
Cow
Chimpanzee t t+
Frog
Monkey
オt+
ャ+
++
KEY:
+++ Heavy Agglutination (Gel Solidification)
+ Medium Agglutination (Thick Liquid)
Slight Agglutination (Flecks)
No Reaction
Lab Questions:
1. Animals that are most closely related to humans exhibited
ichimpanzee agglutination.
Heavy
Medium
Slight
No
2. Animals that show little relation to humans exhibited
cow
agglutination.
Heavy
Medium
Slight
No
3. Which animal is most closely related to humans?
Cow Chimpanzee Frog Monkey
4. Which animal is most unrelated to humans?
Cow
Chimpanzee (Frog Monkey
arrow_forward
Using question 2 you can answer question 3 which I need help with
arrow_forward
1. Compute the volumes needed to complete this table.
Stock
Final
Volume for
Volume for 5x
reaction
Reaction
Component
Concentration Concentration 1x reaction
sddH,0
up to 25 ul
up to 25 ul
Buffer (ViBuffer A)
10X
1X
MgCl,
50 mM
3 mM
DNTP
2 mM
100 uM
forward primer
10 uM
0.2 uM
reverse primer
10 uM
0.2 uM
Taq polymerase
1 U/ ul
1 U/ 25 ul
DNA template
1-2 ng
1 ul
*5X reactions = 2 samples, 1 NTC, 1 positive control, 1 pipetting allowance
arrow_forward
Droplet based single cell DNA sequencing uses a microfluidic platform which
generates droplets encapsulating individual cells. A micrograph of such a device
[Zilionis et al, Nature Protocols 2016] is presented in Figure Q3. The channels are
25 μm deep.
(a)
(b)
Oil
Figure Q3. Micrograph of the microfluidic droplet device. Scale bars are 100 µm.
Adapted from Zilionis et al, Nature Protocols 2016. Red arrowheads show
individual cells, and black arrows indicate flow direction.
(c)
RT/lysis
reagents
Cells
Barcoding hydrogel beads
A company wants to explore the design of a prototype of the device made from
PDMS. Describe a suitable fabrication process, explaining the rationale behind
each individual step. Schematics can be drawn to illustrate your response. You
may want to refer to the datasheets at the end of the script.
Testing of the prototype was successful and the company wants to explore the
feasibility of manufacturing the device from glass. Describe the fabrication
process for this…
arrow_forward
Q4 (a) SDS-PAGE.
Sodium dodecyl sulfate - polyacrylamide gel electrophoresis (SDS-PAGE) is used to identify the molecular weight of unknown protein
samples. Briefly outline the principle of SDS-PAGE.
Marks: 2
For the toolbar, press ALT+F10 (PC) or ALT+FN+F10 (Mac).
BIUS
E v E Y
A
...
Paragraph
Arial
14px
arrow_forward
Hey I am practicing for a molecular biology test and I am having trouble with is practice problem. I am not sure how to set it up to determine the amount of Acid Phosphatase. Can you help?
Determine the amount of Acid Phosphatase in micrograms/ gram wheat germ from the following experimental values. The amount of acid phosphatase found in 198 ul of extract was 8 ug. The amount of extraction buffer used was 8 mL and the amount of wheat germ was 0.8 g.
arrow_forward
Electrophoresis
A protein required 6.8 min to travel 82 cm to the detector in a 96 cm -long capillary tube with 25.4 kV between the ends. Find the apparent electrophoretic mobility.
arrow_forward
what are the volume dilution and dilution factor for bacteriophage A,B,C
arrow_forward
Cytokine Storm (Cytokine Storm) COVID-19The high mortality rate in COVID-19 patients is caused by the occurrence of a cytokine storm (cytokine storm) in the patient's body. This is based on research supported by data obtained, among others, from laboratory results; that there was a significant difference between patients who recovered and those who died. What research data?
Please Answer these following structured questions;
Are cytokines a protein?
How many amino acid residues of human cytokines?
The sequence of the amino acid residues?
Accession number at GenBank ?
Determine the mRNA sequence
Determine the coding sequence
Define the sequence template
What is a Cytokine storm
What research data support the occurrence of Cytokine storm in humans
Answers on paper with source cited provided will be helpful since im new in this part and want to learn from the source you find the answer
Thank you
arrow_forward
How will the information required to describe your RFP be obtained? Which kinds of methods are you going to employ?
lab intro attached if needed
arrow_forward
SEE MORE QUESTIONS
Recommended textbooks for you
Biology: The Unity and Diversity of Life (MindTap...
Biology
ISBN:9781305073951
Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher:Cengage Learning
Related Questions
- Theoretical Data Following the modified protocol for the isolation of Escherichia coli bacteriophage of Encabo (2018) presented below, compute for the pfu/ml of the chloroform-treated lysate. 1ml 1ml 1ml 1ml 1 Chloroform-treated lysate 1ml Dilution 10-3 10-4 10-5 0 0 0 0 0 9ml 9ml 9ml 10-1 10-² 10-3 Empty sterile tubes Incubate inside ref for 15-20min + 0.1 ml lysate-E.coli mix 0.1 ml 9ml 9ml 104 10.5 // 0.1 ml 0.1 ml +0.5 ml E. coli ↓↓↓↓↓↓ Incubate O/N at 35°C, observe for plaques Molten soft agar overlay B. Quantification of the Infective E. coli other Bacteriophage Particles in the Raw Sewage Sample Volume of Stock Plated (in ml) Bottom agar No. of Plaque-Forming Units (pfu) Ave. A B 254 265 132 110 11 23arrow_forwardI am not understanding why TA of alcohol precipitation is used as TA of purified protein. I provided 2 photos, 1 with the questions and the correct answer, and the other photo is a screenshot of the explanation.arrow_forwardAsaparrow_forward
- D Question 9 An enzyme assay of 2 mL of extract shows 7.3 U/mL and a biuret assay shows 4 mg/mL protein on the initial sample. It is salted out and the pellet is washed and resuspended in 0.4 mL buffer. It is re-assayed and shows 12.1 U/mL activity and 1.3 mg/mL protein. What is the change in fold purity for this sample? (answer to 2 decimal places)arrow_forwardCalculate these for 1 ug of plasmid DNA in a final total volume of 20 ul. All enzymes being used here are at a concentration of 10 U/µL. For double digests, give the appropriate volume for each enzyme and decide which buffer to use. (HINT: look up double digest conditions on the NEB website.) You should always calculate all volumes in advance to ensure the correct working concentrations and so that you can prepare the digests as efficiently as possible. It is a good idea to check off each component as it is added to the microfuge tube. Complete the table below, including the volume of DNA sample(s) you will need for 1 pg of the DNA (from two different methods in Experiment #3) based on the concentration(s) you determined from the OD260 value, which you will restriction digest with each of the restriction enzymes singly and in double digests in Part A. For example, the volume of DNA sample that contains 1 µg DNA for DNA sample from Part A, Experiment 3: OD260 = 0.024, dilution 500x…arrow_forwardd/e/1FAIpQLSfTle9UfP15_VUqFI-ACEQd1XBykXv5Lr4dEMQbLJ1d6fCupw/viewform Students subjected three samples of five different molecules to gel electrophoresis as shown in Figure 1 A B C DE +2 3 Wells 4 8. Which of the following statements best explains the pattern seen on the * gel with regard to the size and charge of molecules A and B? 1 point molecules A and B are positively charged, and molecule A is smaller than molecule B. molecules A and B are positively charged, and molecule A is larger than molecule B. molecules A and B are negatively charged, and molecule A is smaller than molecule B. molecules A and B are negatively charged, and molecule A is larger than molecule B. Sign outarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Biology: The Unity and Diversity of Life (MindTap...BiologyISBN:9781305073951Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa StarrPublisher:Cengage Learning
Biology: The Unity and Diversity of Life (MindTap...
Biology
ISBN:9781305073951
Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher:Cengage Learning