DNA Extraction Control 670
CAT# PRODUCT SIZE STORAGE ¼ÒºñÀÚ°¡ ÁÖ¹®
BIO-35028DNA Extraction Control 670500 RXNSat -20¡ÆC-·Î±×ÀÎ
BIO-35029DNA Extraction Control 6702000 RXNSat -20¡ÆC-·Î±×ÀÎ

Features and Benefits

 
Easy monitoring and validation of DNA extraction protocols Detection of real-time PCR inhibition Minimal interference with sample detection Ideal for blood, urine and sputum samples Specially designed for real-time PCR assays
 
 

Instrument Compatibility


DNA Extraction Control 670 is suitable for use with commercially available silica-membrane DNA extraction kits and CHELEX matrices and has been tested on a wide range of real-time PCR platforms including ABI-7500, LightCycler 480¢ç, RotorGene-Q¢â and MX3005P¢ç.

DNA Extraction Control 670 uses Quasar¢ç 670 and is also available with Cal Fluor¢ç Orange 560 or Cal Fluor¢ç Red 610, to fit in with existing protocols. CAL Fluor and Quasar dyes are performance-optimized fluorophores for multiplex real-time PCR.

 

Description


A common practice in real-time PCR is to add a known amount of ¡°spiked¡± control DNA after DNA extraction. This monitors PCR inhibition but has no value as an extraction control. The ideal situation is to have the test sample and internal control undergo the same processing prior to real-time PCR (Fig. 1). Bioline have specially developed a DNA Extraction Control (DEC), which more closely mimics the test sample, as compared to spike controls. The genetic material from the test sample and the DEC is simultaneously extracted by common extraction methods, with the extraction control being as sensitive to inhibition and extraction failure as the test sample.

The DEC cells are of a known concentration, containing the Internal Control DNA sequence. This sequence contains no known homology to any organism and importantly, has minimal interference with detection of sample DNA. The DEC cells are spiked into lysis buffer with the target sample, prior to DNA extraction. Control Mix (primers and probe) is then added to the reaction mix before amplification. Signal derived from the Internal Control DNA confirms the success of the extraction step (Fig. 2). DEC also monitors co-purification of PCR inhibitors (Fig. 3) that may cause biased or false amplification patterns.

DEC offers the quality control assurance required for the entire workflow from sample extraction to real-time amplification and analysis.

 

Components


Internal Control DNA*
Control Mix (containing Quasar¢ç 670 labeled probe)

* The Internal Control DNA is in viable ¥á-Select E. coli cells (genotype: F- deoR endA1 recA1 relA1 gyrA96 hsdR17(rk-, mk+) supE44 thi-1 phoA ¥Ä(lacZYA-argF)U169¬¶80lacZ¥Ä15¥ë–pBR322 (ranseqb1 AmpR)).

Storage Conditions

Stored at –20¡ÆC it is stable for 12 months from date of purchase.
 

Shipping Conditions

Shipped on dry ice or blue ice.

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