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Below you will find a selection of white papers and guides relating to microarrays, PCR and rapidPCR, and other technologies that fall under Core's areas of expertise.

RapidPCR Application Notes

Please contact us for access to the following rapidPCR application notes.

Amplification of microbial strains from soil isolates BS_PCR_01_04_e
Long Range PCR: SpeedCycler amplification of a 24 kb fragment fromhuman genomic DNA (placenta DNA)BS_PCR_02_04_e
One Step RT-PCR using the SuperScriptTM III System with Platinum TaqDNA Polymerase (Invitrogen)BS_PCR_01_05_e
Amplification of a beta globin fragment (210 bp) with BD TitaniumTM TaqDNA Polymerase (BD Biosciences)BS_PCR_02_05_e
Amplification of a beta globin fragment (538 bp) from human genomic DNA BS_PCR_01_06_e
Amplification of a 430 – 750 bp fragment, a tandem repeat at chromosome1 (The D1S80 – system)BS_PCR_02_06_e
Amplification of ITS2 (part of 45S rDNA) from plant BrachycomedichromosomaticaBS_PCR_03_06_e
Amplification of a E.coli specific 536 bp target sequence within 8 min BS_PCR_04_06_e
Multiple (STR) PCR using Applied Biosystem AmpFl STR® SGM Plus® withSpeedCyclerBS_PCR_06_06_e
PCR amplification of a 123 bp fragment from the insertion element IS6110of Mycobacterium tuberculosisBS_PCR_07_06_e
Reliable detection of clinically relevant Staphylococci using the hyplexStaphyloResist® test systemBS_PCR_08_06_e
Amplification of a 129 bp HB Virus specific sequence for Hepatitis Bdetermination by using rapid PCRBS_PCR_09_06_e
Quantitative cPCR considered on the example of Porphyromonasgingivalis wildtype (488 bp) and competitor (276 bp) amplificationBS_PCR_10_06_e
PCR amplification of an Actinobacillus actinomycetem-comitans wild type(547 bp) and competitor (274 bp) specific fragment as optimization toaccomplish cPCRBS_PCR_11_06_e
Optimization of PCR conditions to amplify a specific Treponema denticolawildtyp and competitor sequence to accomplish cPCRBS_PCR_12_06_e
STR Typing by using Promega's PowerPlex® 16 System combined withSpeedCyclerBS_PCR_13_06_e
Amplification of a 641 bp specific Bacteroides forsythus sequence by usingrapid PCR with SpeedCyclerBS_PCR_14_06_e
The enteric Helicobacter bilis as target for rapid amplification withSpeedCyclerBS_PCR_15_06_e
Validation for SNP diagnostics of the Factor V Leiden mutation –Amplification of the relevant sequence with SpeedCyclerBS_PCR_16_06_e
Detection of genetically modified – Roundup Ready® – soybeans by usingrapid PCR with SpeedCyclerBS_PCR_01_07_e
Detection of transgenic Maize by rapid polymerase chain reaction withSpeedCyclerBS_PCR_02_07_e
Determination of Neisseria gonorrhoeae by using rapidPCR withSpeedCycler and two different polymerasesBS_PCR_03_07_e
Amplification of alleles of the HLA-DRB1 gene, optimized for 50 µl-assays BS_PCR_05_06_e
Detection of a human-specific Alu insertion using a PV92 primer mix withSpeedCyclerBS_PCR_04_07_e
Detection of 3 different human-specific beta-globin fragments using 4different primers and the AlphaSCBS_PCR_01_08
Amplification of a 1 kb DNA fragment from the bacteriophage lambdausing the SPR 48 block of AlphaSCBS_PCR_01_09

 

Microarray Spotter (Microarrayer) White Papers and Guides

 

Microarray Scanner White Papers and Guides

 

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