|
|
|
|
LEADER |
01685 am a22002533u 4500 |
001 |
138384.2 |
042 |
|
|
|a dc
|
100 |
1 |
0 |
|a Abudayyeh, Omar O.
|e author
|
100 |
1 |
0 |
|a Broad Institute of MIT and Harvard
|e contributor
|
100 |
1 |
0 |
|a McGovern Institute for Brain Research at MIT
|e contributor
|
100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
|e contributor
|
100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Biological Engineering
|e contributor
|
100 |
1 |
0 |
|a Harvard University-
|e contributor
|
700 |
1 |
0 |
|a Gootenberg, Jonathan S
|e author
|
700 |
1 |
0 |
|a Kellner, Max J.
|e author
|
700 |
1 |
0 |
|a Zhang, Feng
|e author
|
245 |
0 |
0 |
|a Nucleic Acid Detection of Plant Genes Using CRISPR-Cas13
|
260 |
|
|
|b Mary Ann Liebert Inc,
|c 2022-01-06T16:05:34Z.
|
856 |
|
|
|z Get fulltext
|u https://hdl.handle.net/1721.1/138384.2
|
520 |
|
|
|a Nucleic acid detection is vital for agricultural applications including trait detection during breeding, pest surveillance, and pathogen identification. Here, we use a modified version of the CRISPR-based nucleic acid detection platform SHERLOCK to quantify levels of a glyphosate resistance gene in a mixture of soybeans and to detect multiple plant genes in a single reaction. SHERLOCK is rapid (∼15 min), quantitative, and portable, and can process crude soybean extracts as input material for minimal nucleic acid sample preparation. This field-ready SHERLOCK platform with color-based lateral flow readout can be applied for detection and quantitation of genes in a range of agricultural applications.
|
546 |
|
|
|a en
|
655 |
7 |
|
|a Article
|
773 |
|
|
|t 10.1089/CRISPR.2019.0011
|
773 |
|
|
|t The CRISPR Journal
|