IGEM:IMPERIAL/2009/Assays Protocols/Shopping: Difference between revisions

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== Shopping List==
== Shopping List==


* Food grade sodium acetate<br>
* Food grade sodium acetate [http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=S2889|SIAL&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC Sigma Purchasing Page]<br>

Revision as of 02:55, 7 August 2009

Module 1

Cellulase

Link to Assay

Reagents:
Sodium Acetate Buffer, pH 5
- Prepared using Sodium Acetate, Trihydrate, Sigma Prod. No. S-8625 Sigmacell Solution
Cellulase Enzyme Solution
Glucose Determination Vial

Sigma Products for Cellulase Assay:

No. S-8625 = Sodium Acetate, Trihydrate

http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=S8625%7CSIAL&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC


No. S-3504 = Sigmacell Solution (Sigmacell)

http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=S3504%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC


No. 16-10 = Glucose (HK)

http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=GAHK20%7CSIGMA&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&F=SPEC

PAH

Link to Assay

Reagents:
Tris CH1 Buffer
L-Phenylalanine Solution
Catalase Enzyme Solution
DL-Dithiothreitol Solution
6-Methyltetrahydropterine Solution


Sigma Products for PAH Assay:

Trizma Base, Sigma Prod. No. T-1503

L-Phenylalanine, Sigma Prod. No. P-2126

Catalase, Sigma Stock No. C-100

DL-Dithiothreitol, Sigma Prod. No. D-0632

DL-6-Methyl-5,6,7,8-Tetrahydropterine Dihydrochloride, Sigma Prod. No. M-4758

Trichloroacetic Acid, 6.1 N Solution, Sigma Stock No.490-10

Nitric Acid, Aldrich Stock No. 25811-3

Sodium Nitrite, Sigma Prod. No. S-2252

1-Nitroso-2-Naphthol, Sigma Prod. No. N-3765

Sodium Hydroxide Solution, 1.0 N, Sigma Stock No. 930-65

L-Tyrosine Free Base, Sigma Prod. No. T-3754

Module 2

Colanic Acid

Link to Assay Page
Protocol for Quantitative Assay
Qualitative Assay using electron microscopy could be performed as well, to ensure sufficient encapsulation.


Reagents:
No special reagents needed. Centrifuge performed on bacterial media.


Equipment:
PCV Centrifuge Tubes

OtsA

Simple Assay for T6PS (OtsA) and T6PP (OtsB) [1]

Trehalose 6-Phosphate Synthases Catalyses the following reaction:
GDP-glucose + glucose 6-phosphate --> GDP + alpha,alpha-trehalose 6-phosphate

Trehalose 6-Phosphate Phosphatase catalyses the following reaction:
alpha,alpha-trehalose 6-phosphate + H2O --> alpha,alpha-trehalose + phosphate


We will perform the quantitative assay shown above to assess the activity of T6PS and T6PP

Reagents Required:

OtsB Assay

Simple Assay for T6PS (OtsA) and T6PP (OtsB) [1]

Trehalose Assay

Trehalose Assay Method
Link to Assays Purchasing Page

We can test the final OtsAB construct using this simple trehalose assay. The assay is purchased as a kit, with simple step by step instructions to quantify the activity of the enzyme.

Module 3

Heat Induction

Link to Heat Induction Protocols

Visualising SDS -PAGE


Reagents:
Normal SDS-PAGE materials
Nitrocellulose Transfer Membrane
Coomassie Blue R-250
Dimethyl Sulphoxide

Killing Strategy

Measuring Cell Death by counting Colony Forming Units (CFUs)
CFU Method: By knowing the density of cells present in a media using OD measurements, and depositing a set amount of this media (and therefore a set no. of cells) onto an agar plate, we can know the proportion of viable cells still present in our colony after restriction enzyme production. This gives a quantifiable method for the calculation of the efficiency of our killing strategy.


Membrane Staining Assay
Cell Membrane Staining Assay: This assay uses a kit with certain stains to determine whether cells are alive or dead. The assay stains those cells with intact cell membranes green (the 'alive' cells), and those with damaged cell membranes red (the 'dead' cells). This is a quantitative measure of cell death. However, as we are using restriction enzymes, we will not directly affect the cell membrane, so this assay may not work. Natural degredation of the membrane without maintenance from the cell may occur, in which case this would be a useful guide. In either case, it would be useful as an indicator of the viability of the cells with disrupted genetic material. Another issue is the fact that our cells are to be encapsulated, so whether this staining technique can work through the colanic acid capsule is unclear.

Shopping List