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FINAL PROGR AM - American Society of Gene & Cell Therapy

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<strong>AM</strong>ERICAN SOCIETY OF GENE THERAPY • Final Program 151<br />

EXHIBITOR DESCRIPTIONS<br />

Kemp Biotechnologies, Inc.<br />

7307 Governors Way<br />

Frederick, MD 21704<br />

Phone: 301-620-7100<br />

Fax: 301-620-0162<br />

E-Mail: b.miller@kempbiotech.com<br />

www.kempbiotech.com<br />

Booth Number: 407<br />

Kemp Biotechnologies, Inc. will present a proprietary<br />

nontoxic transfection reagent and a proprietary transfection<br />

process, which enables AAV viral vector production<br />

via cotransfection <strong>of</strong> suspension 293 cells. This service is<br />

a scalable, cost-effective alternative to the time-consuming<br />

process <strong>of</strong> transfecting large quantities <strong>of</strong> plates <strong>of</strong><br />

adherent 293 cell cultures to generate AAV vector stocks.<br />

Lark Technologies<br />

9441 W. Sam Houston Parkway South, Suite 103<br />

Houston, TX 77099<br />

Phone: 713-779-3663<br />

Fax: 713-779-1661<br />

E-Mail: sales@lark.com<br />

www.lark.com<br />

Booth Number: 305<br />

Lark, A Genaissance Company is a leading contract<br />

research organization providing research grade and<br />

regulatory submission services including DNA sequencing,<br />

quantitative PCR analysis, and genetic stability<br />

testing. All <strong>of</strong> Lark’s regulatory submission services<br />

comply with Good Laboratory Practices as specified by<br />

the FDA.<br />

Mary Ann Liebert, Inc.<br />

2 Madison Ave.<br />

Larchmont, NY 10538<br />

Phone: 914-834-3100<br />

Fax: 914-834-3771<br />

E-Mail: info@liebertpub.com<br />

www.liebertpub.com<br />

Booth Number: 112<br />

Mary Ann Liebert, Inc. Publishers invites you to come by<br />

our booth #112, and take a complementary copy <strong>of</strong><br />

Human <strong>Gene</strong> <strong>Therapy</strong>, <strong>Gene</strong>tic Testing, <strong>Gene</strong>tic Engineering<br />

News and other related publications.<br />

MDS Pharma Services<br />

2350 Cohen Street<br />

Saint-Laurent (Montreal)<br />

Quebec, H4R 2N6<br />

Canada<br />

Phone: 514-333-0033<br />

Fax: 514-333-8861<br />

E-Mail: info@mdsps.com<br />

www.mdsps.com<br />

Booth Number: 309<br />

MDS Pharma Services’ biopharmaceuticals group<br />

executes rapid and rigorous GLP/cGMP safety and<br />

analytical testing. Our state-<strong>of</strong>-the-art facility in Bothell,<br />

Washington, features restricted-access laboratories and<br />

FDA and ICH compliance. Suites consist <strong>of</strong> BSL-2/BSL-<br />

3 virology labs, cell culture and cell-banking (cGMP)<br />

facilities, protein chemistry and PCR rooms. For more<br />

information, visit www.mdsps.com.<br />

Mirus Bio Corporation<br />

505 S. Rosa Road, Suite 104<br />

Madison, WI 53705<br />

Phone: 608-441-2824<br />

Fax: 608-441-2849<br />

E-Mail: Claire.ruzicka@mirusbio.org<br />

www.mirusbio.com<br />

Booth Number: 505<br />

Mirus Bio provides state-<strong>of</strong>-the-art nucleic acid delivery<br />

and labeling reagents for in vitro and in vivo research.<br />

TransIT â reagents achieve high efficiency/low toxicity<br />

transfections in a variety <strong>of</strong> cell lines and applications<br />

including siRNA delivery. Label IT â non-enzymatic<br />

nucleic acid labeling kits are optimized for hybridization<br />

and tracking applications.<br />

Molecular Medicine Bioservices, Inc.<br />

6219 el Camino Real<br />

Carlsbad, CA 92009<br />

Phone: 760-918-0007<br />

Fax: 760-918-0076<br />

E-Mail: dbacker@molecularmed.com<br />

www.molecularmed.com<br />

Booth Number: 315<br />

Molecular Medicine BioServices, Inc. provides enabling<br />

technologies for viral-based therapeutics. Located in<br />

Carlsbad, CA, the company is a leading contract manufacturing<br />

and clinical production resource for companies<br />

engaged in vaccine and gene therapy development.<br />

Molecular Medicine is committed to supporting clients<br />

from development through production and into clinical<br />

approval.

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