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Revision as of 18:14, 15 May 2014 by Z5011434 (talk | contribs) (Lab 9 Assessment)
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Add your own student page to the site.

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Add a sub-heading

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PubMed

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Laboratory 1

beutiful

Reference

This is about Prokaryote.[1]

<pubmed limit=5>Prokaryote</pubmed>

  1. <pubmed>24603758</pubmed>


Test Image

Chlamydomonas cells in neon.png

Chlamydomonas cells in neon[1]

  1. <pubmed>20076674</pubmed>| PLoS One.

Individual Assessment - Lab 2

Part 1

Progeria Syndrome.png

Hutchinson-Gilford Progeria Syndrome and nucleus[1]

  1. <pubmed>16277559</pubmed>|PLoS One.

--Mark Hill (talk) 14:54, 3 April 2014 (EST) As I mentioned in the lab, you have uploaded an image already on the site and in fact I used in the lecture. I was expecting you to find your own (new) image).

Part 2

Stimulates Emission Depletion (STED) microscopy is a super-resolution microscopy that was used to measure the size of mitochondrial nucleoids. An important feature of this device was that it enabled a resolution of 40 to 50 nm and thus could give a reliable picture of the nucleoid diameter (~100nm - antibody decorated).This form of microscopy is advantageous as no tissue sectioning is necessary which allows the capacity to produce a more realistic image. Using STED microscopy, mitochondrial nucleoids from several mammalian species were analysed and the results showed that all mitochondrial nucleoids had uniform sizes and were often organized in clusters. It was also observed that there was only a single copy of mtDNA present within most mitochondria nucleoids.[1]

  1. <pubmed>21808029</pubmed>

--Mark Hill (talk) 14:56, 3 April 2014 (EST) Very good. Now that we have had the mitochondria lecture, what do you think this paper means?

Individual Assessment - Lab 3

Part 1

ARTICLE 1

I went for a search after old articles that wrote about Nuclear Pore Complex (NPC) so I could grasp some simple concepts about it. “Architecture and Design of Nuclear Pore Complex” talks about its structure and they figured the approximate diameter of the nuclear pore by coating cargo-receptor with gold particles. Division of the nuclear pore into Peripheral and Central channels was also noticed by observing dissected macronuclei from Xenopus laevis oocytes on electron microscopy. In addition, the article tells you about the role these channels play in passive and active transports through nuclear membrane, as well as a picture of their structure.[1]


ARTICLE 2

This article explore the wide role of Nuclear Pore Complex (NPC) on passive and facilitated transports, once this is the only route material can go from nucleus to cytoplasm and vice-versa. The experiment used HeLa cells, where marked molecules were injected. The range of molecules included ones that could go through NPC either by passive diffusion or receptor-mediated routes. It was shown that ions, metabolites and intermediated-sized macromolecules crossed the nuclear membrane by diffusion, whereas proteins, RNA and ribonucleoprotein complexes needed the facilitated transport. It was noticed that though both transports occurred in the central part of NPC they didn't interfere with each other. However, molecules utilizing the same mode of transport affected each other pathways. Hence it was concluded that passive and facilitated transports don't share the same route.[2]


ARTICLE 3

This article investigates the impact of hormones on nuclear permeability. The experiment was made with hepatic cells and several marked molecules were injected in it. It was observed that Ca+ plays an important role when it comes to increase nuclear permeability. They linked this information to the fact that some hormones, such as vasopressin and angiotensin, increase the amount of Ca+ within the nucleus, therefore they concluded that hormones may have a short-term control over the permeability of nucleus membrane.[3]


ARTICLE 4

This interesting article compares the traffic of molecules in health and disease, such as tumour and viral infections. It mentions oncoproteins and tumour suppressor genes and how their balance within the nucleus is important to keep a normal function of the cell, once these genes regulate cell growth and DNA division. Another important point is the role of Nucleuporine 98 (Nup98) and its relation with disease when affected by mutations. Regarding to viral infections, it’s shown that virus can take over export machineries and hinder mRNA from going to cytoplasm and explains why this is beneficial to the virus.[4]


  1. <pubmed>1617726</pubmed>
  2. <pubmed>17164246</pubmed>
  3. <pubmed>17158097</pubmed>
  4. <pubmed>24530809</pubmed>

Part 2

Structures of Caldedrin and Jacob.png

Calderin and Jacob, proteins involved in nucleus signaling[1]

  1. <pubmed>18303947</pubmed>|PLOS Biology.


Individual Assessment - Lab 4

-Anti-Nuclear Pore Complex Proteins antibody (ab73291)

-The antibody derives from Rabbit

-working concentration depends on the different types of application

Application

WB------>Use a concentration of 1 - 2 µg/ml

ICC/IF-->Use a concentration of 20 µg/ml.

ICC----->Use a concentration of 2.5 µg/ml.

-paper that uses this antibody

[1]

  1. <pubmed>23667637</pubmed>

Lab 9 Assessment

1. Write a hypothesis that you are going to test.

Large quantities of cytochrome C will be detected in the cytoplasm of the cell which can only be released via the intrinsic pathway during apoptosis.

2. Write aims of your experiment.

To measure the amount of cytochrome C within the cytoplasm.

3. Identify key techniques and procedures used in your investigation (Spell these out in some detail).

Centrifugation – To separate the supernatant from the tissue culture. Western blotting – analytical technique used in this experiment to detect cytochrome C.

4. Identify suppliers that have resources that you will need for your study (create links to the supplier resource pages, kits, antibodies etc).

CytoPainter Mitochondrial Staining Kit - Green Fluorescence

Cytochrome c Antibody

Cytochrome C ELISA Kit


5. Now prepare a flow diagram of how the experiment will be carried out and analysed.

Tissue -> Add 1ml of mitochondria Extraction Buffer and 1 ml of Cytosol Extraction Buffer individually -> Centrifuge -> Wash cells with PBS Incubate on ice -> Homogenize cells in an ice-cold dounce tissue grinder -> Collect supernatant as Cytosolic Fraction and Mitochondrial Fraction -> Load 10 μg of each cytosolic and mitochondrial fraction on a 12% SDS-PAGE Western blotting and probe with cytochrome c antibody.

6. What will different experimental results (outcomes) mean.

After using the Assay kit we will see a large amount of Cytochrome C within the Cytoplasm, and by analysing the Mitchondria, we will see pores formed on the outer membrane. Thus, proving that Apoptosis occurred due to the Intrinsic Pathway.