User:Z3252261

From CellBiology

Lab 1

The Journal of Cell Biology, BMC Cell Biology, Public Library of Science allow reuse of acknowledged and correctly cited content.--Dougall Norris 03:33, 17 March 2010 (UTC) --Dougall Norris 05:52, 17 March 2010 (UTC)

Lab 2

The lighter staining areas in the nucleus are euchromatin.--Dougall Norris 05:24, 24 March 2010 (UTC)

Lab 3

Seek Australian OHS, Australian acts and standards and Material Safety Data Sheets--z3252261 06:40, 24 March 2010 (UTC)

Lab 4

anti-Cadherin 2, Type 1, N-cadherin (neuronal) (CDH2) antibody, binds to neural cadherin protein. [1]--Dougall Norris 05:56, 31 March 2010 (UTC)

Lab 6

ZDougs.JPG --Dougall Norris 08:05, 21 April 2010 (UTC)


Lab 7

Present :) --Dougall Norris 06:53, 28 April 2010 (UTC)

(1)Air allows for the fastest viewing of all objectives, with no clean up but the least resolution (Refactive indice of 1.0),
(2)Water objectives allow for higher resolution (Refactive indice of 1.33) that air and also permit live specimens to be viewed in aqueous solutions, and
(3)Oil provides the highest resolution of all objectives (Refactive indice of 1.5), yet the cell must be fixed and stained, thus it is the most time consuming.


Lab 8

present --Dougall Norris 06:34, 5 May 2010 (UTC)

Oh yeah Mark, i have been here every week but i didnt start marking that i was present until last week. You told me to make a note of that on my page, and that i should hope that you trust me based on my posts for every other lab. Here is that note, thanks a lot.--Dougall Norris 06:37, 5 May 2010 (UTC)

Commented on group 1s page--Dougall Norris 07:10, 9 May 2010 (UTC)

Commented on group 2's page--Dougall Norris 01:33, 10 May 2010 (UTC)

Commented on group 4's page--Dougall Norris 01:06, 11 May 2010 (UTC)

Commented on group 3's page--Dougall Norris 01:25, 11 May 2010 (UTC)

Commented on group 6's page--Dougall Norris 06:13, 11 May 2010 (UTC)

Commented on group 7's page--Dougall Norris 06:40, 11 May 2010 (UTC)

Commented on group 8's page--Dougall Norris 06:59, 11 May 2010 (UTC)

Commented on group 9's page--Dougall Norris 07:14, 11 May 2010 (UTC)

Commented on group 10's page--Dougall Norris 13:17, 11 May 2010 (UTC)


Lab 9

Present--Dougall Norris 08:00, 12 May 2010 (UTC) The technological bottleneck common to all generation sequencing (NGS) platforms is that DNA library preparation and data analysis are highly time consuming and its also prone to data loss.

Lab 10

Present--Dougall Norris 07:01, 19 May 2010 (UTC)