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5-HTP 100mg
5-HTP 50mg
Acai Extract
ALA/ALC/Carnosine/GSE
Anti-Aging MultiPack
B-12, Sublingual
B-Complex
Blood Pressure Support
Calcium Magnesium
Children's Chewable Vitamin
Cholesterol Therapy
CLA
CoEnzyme Q10
Curcumall
DHEA 10mg
DHEA 25mg
Digestive Matrix
EPA/DHA 180/120
Evening Primrose Oil
GABA, 500 mg
Grape Seed Extract
Green Tea Extract
Immune Formula
Juice Complex
Kardea banana nut bar
Kardea bar, lemon ginger
Kardea chai spice bar
Kardea cranberry almond bar
Longevity MultiPack
Magnesium Glycinate
Mega EPA/DHA 420/280
Mega Probiotic, Non-Dairy
Melatonin
Memory Support
Milk Thistle
Mood Support
Phosphatidylcholine
Plant Sterols
Prostate Support
Red Yeast Rice, 900 mg
Resveratrol 250mg
Resveratrol 50mg
Shake Variety Box (30)
Shake Variety Pack (3) with Cup
Shaker Cup
Soy Isoflavones
Supreme Berry
Supreme Chocolate
Supreme Vanilla
Thyroid Support
TMG
Total Care Daily Formula
Total Eye Care
Total Joint Care
Two-a-Day Multiple
Ubiquinol, 50mg
V-Pure
Vitamin C 1000mg
Vitamin D3, 1500IU
Vitamin E
Women's Hormone Support


Healthy Headlines

12/20/2009
Faster and Cheaper DNA Sequencing

In a study published in the Dec. 20 online edition of Nature Nanotechnology, a team led by Boston University Biomedical Engineering Associate Professor Amit Meller details pioneering work in detecting DNA molecules as they pass through silicon nanopores. The technique uses electrical fields to feed long strands of DNA through four-nanometer-wide pores, much like threading a needle. The method uses sensitive electrical current measurements to detect single DNA molecules as they pass through the nanopores.

"The current study shows that we can detect a much smaller amount of DNA sample than previously reported," said Meller. "When people start to implement genome sequencing or genome profiling using nanopores, they could use our nanopore capture approach to greatly reduce the number of copies used in those measurements."

Currently, genome sequencing utilizes DNA amplification to make billions of molecular copies in order to produce a sample large enough to be analyzed. In addition to the time and cost DNA amplification entails, some of the molecules - like photocopies of photocopies - come out less than perfect. Meller and his colleagues at BU, New York University and Bar-Ilan University in Israel have harnessed electrical fields surrounding the mouths of the nanopores to attract long, negatively charged strands of DNA and slide them through the nanopore where the DNA sequence can be detected. Since the DNA is drawn to the nanopores from a distance, far fewer copies of the molecule are needed.

More info: http://www.physorg.com/news180531065.html

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