Method for avoiding PCR-inhibiting contaminants when eluting DNA from polyacrylamide gels

BioTechniques

Volumn 29, Issue 4, 2000, Pages 694-696

  Etokebe, G E ^a   Spurkland, A ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

AGAROSE; DNA FRAGMENT; POLYACRYLAMIDE GEL; WATER;

CONTAMINATION; DNA DENATURATION; DNA PURIFICATION; GEL ELECTROPHORESIS; GENE AMPLIFICATION; POLYMERASE CHAIN REACTION; SHORT SURVEY; TEMPERATURE;

EID: 0033793392     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/00294bm04     Document Type: Short Survey

References (7)

1. Complementary strand analysis: A new approach for allelic separation in complex polyallelic genetic systems
2. Locus-specific amplification of HLA class 1 genes from genomic DNA: Locus specific sequences in the first and third introns of HLA-A, -B and -C alleles
3. HLA-B typing by allele separation followed by direct sequencing
4. Rapid and inexpensive micro-elution of nucleic acid and protein from agarose and polyacrylamide gels
5. Amplification of differentially displayed PCR products isolated from untreated denaturing polyacrylamide gels
6. Rapid method for the elution and analysis of PCR products separated on high resolution acrylamide gel
7. Electrophoresis gel media: The state of the art