PCR-genotyping of barley seedlings using DNA samples from tissue prints

Plant Breeding

Volumn 121, Issue 3, 2002, Pages 228-231

  Drescher, A ^a   Graner, A ^a  

^a LEIBNIZ INSTITUTE OF PLANT GENETICS AND CROP PLANT RESEARCH IPK   (Germany)

Author keywords

DNA isolation; FTA paper; High throughput screening; Hordeum vulgate; PCR

Indexed keywords

EMBRYOPHYTA; HORDEUM; HORDEUM VULGARE SUBSP. VULGARE;

EID: 0036305628     PISSN: 01799541     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1439-0523.2002.00660.x     Document Type: Article

References (14)

1. DNA elution and amplification by polymerase chain reaction from dried blood spots
2. A simple and rapid method for the preparation of plant genomic DNA for PCR analysis
3. Molecular mapping of genes conferring resistance to viral and fungal pathogens
4. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants
5. Molecular mapping of a new gene in wild barley conferring complete resistance to leaf rust (Puccinia hordei Otth)
6. A plant isolation protocol suitable for polymerase chain reaction based marker-assisted breeding
7. Detection of plant genes using a rapid, nonorganic DNA Purification method
8. Enhanced direct amplification of Guthrie card DNA following selective elution of PCR inhibitors
9. Rapid isolation of high molecular weight DNA
10. Gene amplification directly from Guthrie blood spots
11. Extraction of DNA from milligram amounts of fresh, herbarium and mummified plant tissues
12. Microwave extraction of total genomic DNA from barley grains for use in PCR
13. Single-step protocol for preparation of plant tissue for analysis by PCR
14. A simple method of preparing plant samples for PCR