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Cold Spring Harbor Laboratory


Zinc finger nuclease, immunoprecipitation methods featured in Cold Spring Harbor Protocols

A protocol for detecting targeted chromosomal deletions induced by zinc finger nucleases allows researchers to estimate the frequency of ZFN-induced genomic deletions using PCR-based methods. Immunoprecipitation is also optimized with detailed instructions for lysis conditions, protease inhibitor cocktails, and general preparation.

SourceCold Spring Harbor Laboratory·JournalCold Spring Harbor Protocols·DateAug 2, 2010

May's Cold Spring Harbor Protocols features plant gene expression methods, Xenopus imaging

Cold Spring Harbor Laboratory has published new methods for plant gene expression and Xenopus imaging, enabling faster and more efficient investigation of gene function. These protocols utilize Agrobacterium-mediated transformation and confocal microscopy to study cellular behavior and subcellular processes in plants and frog embryos.

SourceCold Spring Harbor Laboratory·JournalCold Spring Harbor Protocols·DateMay 3, 2010

Protein-bait interactions, display libraries featured in Cold Spring Harbor Protocols

Researchers from the Broad Institute of MIT and Harvard present a new method for identifying protein-bait interactions, allowing for sensitive detection and discrimination of specific interactions. The method uses quantitative proteomics approaches to compare enrichment with the bait of interest against samples using control baits.

SourceCold Spring Harbor Laboratory·JournalCold Spring Harbor Protocols·DateMar 1, 2010

CSHL study identifies potential way to reverse cancer cell metabolism and tumor growth

A study at Cold Spring Harbor Laboratory has identified three molecular factors that contribute to high levels of PK-M2 in cancer cells, which promotes rapid cell proliferation and tumor growth. The researchers found that forcing a reduction in the levels of these factors could reverse the Warburg effect and restore normal metabolism.

SourceCold Spring Harbor Laboratory·JournalProceedings of the National Academy of Sciences·DateJan 22, 2010

CSHL scientists use next-gen sequencing to rapidly discover genetic cause of devastating disorder

Scientists from CSHL and Hebrew University Medical Center use next-gen sequencing to rapidly identify the mutated TMEM216 gene as the cause of Joubert Syndrome. The study reveals a high carrier rate of 1:92 among Ashkenazi Jews, making it possible to prevent the disease through premarital genetic screening.

SourceCold Spring Harbor Laboratory·JournalAmerican Journal of Human Genetics·DateJan 13, 2010