User:Z3178608

From CellBiology

ANAT 3231 Student's Individual Project --z3178608 05:44, 10 March 2010 (UTC)


Lab 1 - What Cell Biology Journals allow reuse of acknowledged and correctly cited content?

The Journal of Cell Biology, BMC Cell Biology and Public Library of Science allow reuse of content provided the article is properly cited.


Lab 2 - What are the "light" regions of DNA within the nucleus called?

euchromatin --z3178608 06:50, 17 March 2010 (UTC)


Lab 3 - How do we know the hazards associated with research chemicals?

Material Safety Data Sheets (MSDS) are a set of standardised safety information prepared for each of the chemicals used within the laboratory.

--z3178608 06:40, 24 March 2010 (UTC)


Lab 4 - Identify a commercially available antibody to an adhesion junction protein, and also add a link to the antibody page on your own student

Murine monoclonal anti-VAP-1 IgM antibody vepalimomab binds to the binding to the extracellular domain of the vascular adhesion protein (VAP-1). http://www3.interscience.wiley.com/cgi-bin/fulltext/118719049/PDFSTART --z3178608 05:52, 31 April 2010 (UTC)


Lab 5 - Complete the knockout methods handout given out in the laboratory.

Graph






















--z3178608 08:20, 21 April 2010 (UTC)


Lab 7 - From today's confocal tutorial, identify an advantage to using each of the following objectives: Air, Water or Oil.

  • Air: Minimum hazzle
  • Water: Reducing spherical aberration; allowing application on living cells and tissues.
  • Oil: Increases the resolution of the microscopic image at high magnification; insensitivity to cover slip thickness.

--z3178608 10:42, 28 April 2010 (UTC)


Lab 8 - Your assessment item is to critically review all other group projects. Use the Group Assessment Criteria as discussed in the lab. Record your peer assessments on each group talk page, with your signature. Add the project title and a brief comment to your own page.

I have assessed Group 2 project page titled RNA interference.

--z3178608 07:36, 5 May 2010 (UTC)

I have assessed Group 3 project titled immunohistochemistry.

--z3178608 10:56, 10 May 2010 (UTC)

I have assessed Group 4 project page titled cell culture.

--z3178608 11:24, 10 May 2010 (UTC)

I have assessed Group 5 project page titled electron microscopy.

--z3178608 11:43, 10 May 2010 (UTC)

I have assessed Group 6 project page titled confocal microscopy.

--z3178608 22:20, 10 May 2010 (UTC)

I have assessed Group 7 project page titled monoclonal antibodies.

--z3178608 22:44, 10 May 2010 (UTC)

I have assessed Group 8 project page titled microarray.

--z3178608 04:19, 11 May 2010 (UTC)

I have assessed Group 9 project page titled fluorescent proteins.

--z3178608 04:40, 11 May 2010 (UTC)

I have assessed Group 10 project page titled somatic cell nuclear transfer.

--z3178608 05:02, 11 May 2010 (UTC)



Lab 9 - Microarray Lab: What is the technological bottleneck common to all next generation sequencing (NGS) platforms?

The technology bottleneck common to all NGS platform is the intrinsic limitation in sequencing highly repetitive regions, owing to the short lengths of DNA produced by these systems. This is the major drawback that limits their use especially in de novo sequencing.

--z3178608 23:13, 14 May 2010 (UTC)