e-Lynx - April 2008

Dear Researcher,

We are pleased to present the April e-Lynx, a newsletter devoted to keeping our customers up-to -date on new technologies, our new products, suppliers, activities and promotions.

New Products and Services

Active Motif - Suspension Cell FACE™
Adapt any FACE kit for use with non-adherent cells

Active Motif’s FACE™ Kits provide a simple cell-based method to assay for phosphorylated protein targets. The Suspension Cell FACE module enables you to take advantage of the optimized FACE Kits while adapting them for improved results when working with non-adherent cell models. The Suspension Cell FACE module was designed to be used with any colorimetric or chemiluminescent FACE Kit; it provides you with 96-well filter plates that make it easier to perform washing & liquid handling steps through use of an appropriate vacuum manifold.

Simply substitute the filter tissue culture plates for the standard 96-well plates supplied with FACE Kits, and use the Suspension Cell Blocking Buffer in place of the Antibody Blocking Buffer. In addition, fluorescent Hoechst stain is included for normalizing results, as the Crystal Violet stain included in FACE Kits stains the filters of the 96-well filter plates.

Click here for more information on Active Motif FACE kits

Product Number Description Pkg Size
AM48305 Suspension Cell FACE™ 2 x 96 rxns
AM48405 Suspension Cell FACE™ Chemi 2 x 96 rxns

Macherey-Nagel - Protino® Glutathione Agarose 4B

Protino® Glutathione Agarose 4B enables fast and convenient purification of recombinant Glutathione-S-Transferase (GST)-tagged proteins from whole cell extracts by affinity chromatography.

Binding of protein is based on the selective interaction between the Glutathione-S-Transferase tag of the recombinant protein and the immobilized glutathione of the affinity resin. The binding process is highly specific and selective as it is based on an enzyme-substrate reaction between GST and its substrate glutathione, a tripeptide. Thus, only one chromatographic step leads to a high degree of purification. Elution of the GST-tagged protein is performed with free glutathione in the elution buffer. The affinity of Glutathione-S-Transferase for free glutathione is higher than the one for the immobilized glutathione bound to the agarose matrix. Therefore free glutathione replaces the immobilized glutathione which leads to release of the GST-tagged protein from the matrix.

  • High flexibility – for batch, gravity flow and FPLC purification
  • Universal Use – Suitable for small proteins, large protein complexes, proteins with low expression rates.
  • A cost effective alternative for GST-tag purification
Product Number Description Pkg Size
MCN74550010 Protino® Glutathione Agarose 4B 10 mL
MCN745500100 Protino® Glutathione Agarose 4B 100 mL

Associates of Cape Cod Inc. - Pyros EQS Software
The Pyros EQS is intuitive, easy-to-use software that is designed specifically for endotoxin testing with the Pyros Kinetix tube reader.

Pyros EQS is a sophisticated 21 CFR Part 11 Compliant, software solution that provides efficient, accurate analysis and reporting. The software writes to an *Oracle® database, the industry standard in data security. It has multiple access levels for improved security, detailed audit trails, and built-in trending by date range, technician, sample type and LAL lot. The software provides enhanced reporting options, flexible operation modes and incorporates electronic signatures, as well as a supervisor sign-off on completed tests. The application also offers two choices for calculating Coefficient of Variations (CVs), and a new summarized Pass/Fail Report. For users who do not require 21 CFR Part 11 compliance, a more affordable version without the compliance features is also available.

Click here for the product brochure.

Product Number Description Pkg Size
SKPEQS11 Pyros EQS Software with Manual
(21 CFR Part 11 Compliant)
Each
SKPEQS Pyros EQS Software with Manual
(Without Part 11 Compliance Features)
Each

Active Motif - HDAC Assay Kit
Colourimetric or fluorescent assays for histone deacetylase activity

HDAC (Histone Deacetylase) Assay Kits are 96-well plate-based assays to determine the HDAC activity in your extracts or purified samples. HDAC Assay Kits are available in both colourimetric and fluorescent formats to suit your needs.

Each HDAC Assay Kit contains positive control HeLa Nuclear Extract, deacetylated HDAC assay standard, HDAC peptide substrate, Trichostatin A as a model inhibitor and all the essential buffers for a full 96-well plate assay.

  • Works with Class I and Class II HDAC enzymes
  • Easy to adapt to work with Class III HDAC enzymes
  • Use nuclear extracts, immunoprecipitates, column fractions or purified proteins
  • Calculate enzymatic activity and screen inhibitor compounds
Product Number Description Pkg Size
AM56200 HDAC Assay Kit (Fluorescent) 1 x 96 rxns
AM56210 HDAC Assay Kit (Colourimetric) 1 x 96 rxns

 

 

New Literature

Polyplus Transfections - 2008 Catalogue

Polyplus Transfections offers reagents for intracellular delivery of biomolecules. They offer products for in vitro and in vivo delivery of genes, oligonucleotides, siRNA, proteins, antibodies and peptides.

 

Promotions

Macherey-Nagel - iPod® Promotion

Until June 30, 2008
Take advantage of special pricing on
NucleoSpin® Kit Bundles
AND receive a FREE iPod nano

 

Click here for details

Offer valid from March 1st to June 30th, 2008
Cannot be combined with any other offers or discounts
Promotional Code MCNI08

 

Abgent - 40% OFF Newly Released Antibodies

Abgent strives to provide you with an expansive and unique antibody collection for advancing your research.

Abgent now offers huge savings on new products.
Click here for a listing of applicable products and promotion details

 

Assay Designs - Buy 3, Get 1 Free - Antibody and Protein Promotion

Offer extended until December 31st, 2008

Fall into savings with this buy 3, get 1 free promotion on Assay Designs top selling antibodies and proteins. All you need to do is select at least 4 Assay Designs™ antibodies or proteins from the list below and you will receive the lowest priced product free of charge.

  • Over 110 antibodies and proteins to choose from, including many Stressgen® brand products
  • Diverse set of research areas including heat shock, cell signaling, oxidative stress, and inflammation
  • Superb performance documented in thousands of peer-reviewed publications

Click here for promotion details

Valid until December 31st, 2008 or while quantities last
Promotional Code: EOY112607
Cannot be combined with any other offers or discounts

Technical Report

The CometAssay™: A Tool for Measuring DNA Repair
by Trevigen

The single cell gel electrophoresis or CometAssay™ is a state of the art technique for quantitating DNA damage and repair from in vivo and in vitro samples of eukaryotic cells and some prokaryotic cells. This technique is rapid, non-invasive, sensitive, visual and inexpensive compared to conventional techniques and is a powerful tool to study factors modifying mutagenicity and carcinogenicity. It is the only technique that directly measures DNA damage in individual cells and as a result has rapidly gained importance in the fields of genetic toxicology and human biomonitoring. The CometAssay™ measures double strand breaks (DSBs), single strand breaks (SSBs), alkali labile sites, oxidative DNA base damage, DNA-DNA/ DNA-protein/DNA-Drug crosslinking and DNA repair.

During the course of cancer treatment tumor cells frequently become resistant to the therapeutic agent. When this happens it is frequently not possible to administer a high enough dose of chemotherapeutic drugs to overcome the resistance of the cancer cells since the patient cannot tolerate the dose. Resistance to the effects of chemotherapeutic drugs frequently is a result of the tumor's ability to overcome the damaging actions of the therapy (1).

At the core of this resistance are the DNA repair mechanisms and or cellular pumps that export drugs from the cell before they can reach the nucleus. DNA repair pathways maintain genome integrity by repairing adducts and breaks. These same repair pathways confer resistance to the cancer killing effects of the most established therapies. It would therefore seem logical that an effective form of cancer treatment would involve the nontoxic inhibition of one or more DNA repair pathways to increase the effectiveness of therapeutic agents. There is evidence that drugs that inhibit one of these pathways in such tumors may be useful agents in the treatment of cancer.

The CometAssay™ is ideally suited to evaluate compounds that affect cellular DNA pathways. In the study below using both the alkaline CometAssayTM and the neutral CometAssay™ we demonstrate the effect of the PI3 kinase inhibitor, wortmannin on the repair of double strand breaks in DNA. PI3 kinases are activated in the presence of double strand DNA breaks and are critical to the Non Homologous End Joining (NHEJ)
pathway.

In figure 1, Jurkat cells were incubated in the presence of escalating concentrations of the topoisomerase inhibitor etoposide for 2 hours. Subsequent to treatment, the percent DNA in the tail and comet tail length were determined using both neutral and alkaline CometAssay™ procedures. Table 1 shows the results of experiments in which Jurkat cells were treated with etoposide and then permitted to repair damaged DNA in the presence or absence of wortmannin. In these experiments cells were washed to remove etoposide and then permitted to recover for 1 hour. As judged by the neutral CometAssay™, etoposide treated cells in the absence of the PI3K inhibitor wortmanin, underwent DNA repair as comet length and percent DNA in the tail returned to the same value as that of the untreated controls. However, CometAssay™ parameters for etoposide treated cells incubated in the presence of wortmannin remained unchanged indicating that NHEJ was inhibited during the 1 hour recovery period. The data is a good example of the utility of the CometAssay™ as a tool for measuring DNA repair and for the evaluation of compounds that interfere with specific DNA repair pathways.

Figure 1 - Exposure to Jurkat Cells to Etoposide

Table 1 - Effect of Wortmannin on DNA Repair

References:
1. Helleday, T., Petermann, E., Lundin, C., Hodgson, B. and Sharma, R.A.
2008. Nature Reviews Cancer 8: 193-204.

Ordering Information:

Product Number Description
TV4250050K CometAssay™ Kit
TV4251050K CometAssay™ Silver Kit
TV4252040K High Throughput CometAssay™ Kit
TV4253096K CometAssay™ 96
TV4256010CC CometAssay™ Control Cells

Tradeshows

Visit MJSBioLynx at the following events:

Tradeshow Location Date
Minishow - Carleton University Carleton University
Nesbitt Biology Bldg. Lobby
Ottawa, On
April 3rd, 2008
10:00 am - 2:00 pm
Rendez-vous Protéomique McGill University
Leacock Bldg.
Montreal, Qc
April 10th, 2008
Minishow - Canadian Food Inspection Agency Fallowfield Location
First Floor Teaching Lab

April 22nd, 2008
10:00 am - 2:00 pm

 

Tech Support Link
 
1-888-593-5969
P.O. Bag 1150, 300 Laurier Blvd., Brockville, Ontario, Canada, K6V 5W1, Fax: (613) 342-1341

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