OK - have managed to find a version of the paper here.
http://projects.nfstc.org/workshops/resources/literature/Amplification/35_The%20Effect%20of%20Luminol%20on%20Presumptive%20Tests%20and.pdfWhilst on the subject, the following explanation of LCA DNA may be helpful. (Apologies for cut and paste)
DNA
The standard DNA test (SGM+) is used where an identifiable stain such as blood or semen is found. The smallest bloodstain visible with the naked eye (c. 50 - 100 cells) contains enough DNA for this test.
This analyses eleven areas (also called markers or loci) of DNA, consisting of ten variable areas and a sex test.
These areas are copied 28 times and instrumental analysis used to capture and analyse the result.
This test is used to produce DNA profiles for adding to the National DNA Database (NDNAD).
This type of test is used worldwide, and a variety of commercial systems looking at different areas (markers, loci) of DNA are available.
Some samples are invisible to the naked eye, in poor condition due to external factors e.g. fire and water, or have been retained from crimes that occurred many years ago. These may have too little DNA for the standard test to be successful.
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How the Low Copy Number (LCN) technique works
The LCN test is based upon the same scientific principles as the standard SGM+
test, with variations designed to increase the sensitivity of the process, including copying the DNA sample 34 times rather than the standard 28.
The test can obtain a profile from as few as 5 - 10 cells, or from DNA that is in poor condition. This could be the amount of DNA left on a cup by drinking from it or on a pen by writing with it.
This increased sensitivity means ultra-clean laboratories are needed for the testing to minimise contamination of the sample by DNA from any other source.
Rather than performing a separate quantitation stage, a dilution stage is now included routinely to ensure that nothing else present in the sample has caused the result to be lost.