User:Z3329502

From CellBiology

Lab 1 Answer

The Journal of Cell Biology (if the article is more than 6 months old), BMC Cell Biology and Public Library of Science allow the reuse of content, conditional on a full citation. --Louisa Frew 01:37, 11 March 2010 (UTC)

hi --z3329502 05:45, 10 March 2010 (UTC)

Lab 2

The light regions of DNA in the nucleus are called euchromatin. It consists of loosely packed and transcriptionally active DNA, as opposed to the dark "heterochromatin" DNA. --Louisa Frew 06:44, 17 March 2010 (UTC)

Lab 3

To find information of the hazards associated with chemicals you need to consult the Material Safety Data Sheet (MSDS) for each chemical. The MDMS gives information on the various names of the substance and it's chemical and physical properties as well health hazard information and the necessary precautions that need to be excerised for safe handling. The MSDS is available in either hard or electronic copy in all UNSW labs. --Louisa Frew 06:51, 24 March 2010 (UTC)

Lab 4

A monoclonal, anti-E cadherin antibody produced in rat hosts. Reactive in Murine and Canine species for use in Western Blotting, Immunohistochemistry of frozen sections and Immunoprecipitation.

http://www.antibodies-online.com/antibody/146178/anti-E+Cadherin/ --Louisa Frew 05:57, 31 March 2010 (UTC)

Lab 6

Z3329502 graph.JPG --Louisa Frew 07:56, 21 April 2010 (UTC)

Lab 7

The advantages of each type of objective for microscopy:

1) Air- requires no extra preparation of the slide, eliminates the mess invloved with using water and oil 2) Water- good for the imaging of live cells suspended in an acqueous medium due to the relatively similar refractive indexes. Water provides a higher resolution then the air objective due to it's refractive properties, but the resolution isn't as high as that obtained by using an oil objective. 3)Oil- gives the highest resolution of the three different objectives but requires cells to be fixed --Louisa Frew 12:17, 1 May 2010 (UTC)

Present Lab 8 --z3329502 08:09, 5 May 2010 (UTC)

Assessed Group 1 Project --z3329502 07:46, 5 May 2010 (UTC)

Assessed Group 2 Project

Assessed Group 5 Project --z3329502 08:09, 5 May 2010 (UTC)

Assessed Group 3 Project

Assessed Group 4 Project --Louisa Frew 13:55, 8 May 2010 (UTC)

Assessed Group 6 Project --Louisa Frew 14:14, 8 May 2010 (UTC)

Assessed Group 8 Project --Louisa Frew 14:32, 8 May 2010 (UTC)

Assessed Group 7 Project

Assessed Group 10 Project --Louisa Frew 11:48, 9 May 2010 (UTC)

Lab 8

Apologies for the late submission, I forgot to check back for the question after the lab! My answer- the common bottle-neck is the ability to process the data through the use of bioinformatics and having computers that can store the large amounts of data generated.--Louisa Frew 13:32, 18 May 2010 (UTC)