Enzyme and buffer can be stored for up to 12 months at -20˚C.
Kits include KAPA Express Extract Enzyme (1 U/µL) and Buffer (10X).
For Research Use Only. Not for use in diagnostic procedures.
KAPA Express Extract Kit is a novel thermostable protease and buffer system that allows for the extraction of PCR-ready DNA in as little as 15 minutes. DNA extractions are conveniently performed in a single-tube thereby greatly reducing the risk of sample loss and contamination.
The combination of KAPA Express Extract and KAPA2G Robust HotStart ReadyMix provides a high performance solution for rapid DNA extraction and consistent downstream amplification.
View KAPA Express Extract Kit performance data showing high-quality PCR products and the sequencing data obtained using them.
Figure 2. DNA was extracted with KAPA Express Extract Kit from various samples obtained from mammals and fish. From each extract, 2 µL was used directly (without quantification) in a PCR containing KAPA2G Robust HotStart ReadyMix and primers for the ~650 bp cytochrome c oxidase I gene fragment. PCR products (10 µL) were analyzed in a 1% agarose gel. Sample origin and type is displayed above the gel. Reaction products were used directly in standard Sanger sequencing reactions using out-nested M13 primers (2 µL PCR product per 10 µL sequencing reaction). Sequence data was of a high quality and enabled the identification of each species. A section of the sequence trace from Seriola lalandi (Yellowtail amberjack) tissue is presented in the bottom panel.
View data comparable to purified human genomic DNA obtained from FFPE samples showing high PCR yields and successful sequencing results using the KAPA Express Extract Kit.
Figure 3. DNA extracts were prepared from two different FFPE samples using KAPA Express Extract. Each extract was used directly (without quantification) in multiple PCRs containing KAPA2G Robust HotStart ReadyMix and primers for five different fragments (293 bp - 1 kb) of the EGFR gene (corresponding to exons 18 - 21 and 24). Results were compared to those obtained using the same reaction and cycling conditions but using 1 ng purified human genomic DNA as template. With the exception of the 1 kb exon 24 fragment from the older sample, yields and reaction efficiencies were comparable between the FFPE DNA extracts and purified genomic DNA. The PCR products generated from sample 1 were diluted 1:10 and used directly in standard Sanger sequencing reactions. Sequence data (bottom panel, Sample 1 exon 19 fragment) was of a high quality. The mixed sequence starting at the position marked with the arrow confirmed the presence of a 15-nt deletion associated with non-small cell carcinoma diagnosed in the patient from whom Sample 1 was collected.
Figure 4. Extraction and amplification of DNA from different blood sample types for detection of the HLA-B*27 allele. DNA was extracted from 12 human EDTA blood samples with KAPA Express Extract (top panel). 2 µL of each extract was added directly to a 25 µL PCR containing KAPA2G Robust HotStart ReadyMix and two primer sets. The internal control primer set targets a 429 bp fragment of the beta globin gene, whereas the second primer set targets a 141 bp fragment of the HLA-B*27 locus in a sequence-specific manner. Two of the 12 individuals tested positive for the HLA-B*27 allele associated with ankylosing spondylitis. Lanes C- and C+ represent HLA-B*27 negative and positive controls respectively (1 ng purified human genomic DNA as template). DNA was extracted from “Guthrie” cards, FTA cards, or FTA Elute cards (bottom panel) spotted with blood of individuals confirmed to be HLA-B*27 positive (+) or negative (-). DNA extraction and amplification conditions and controls (C- and C+) were the same as for the top panel.
*Data on file.
|Kit Code||Roche Cat. No||Description||Kit Size|
||Standard kit, 100 U
||Standard kit, 200 U||100 reactions
||Standard kit, 500 U
||Standard kit, 1000 U
||Standard kit, with PCR, 200 U
||Standard kit, with PCR, 1000 U
For which applications should I use the KAPA Express Extract Kit?
The KAPA Express Extract Kit is ideally suited for the extraction of DNA from crude samples for most PCR applications, including qPCR analysis; however, residual inhibitors may result in a quenching of commonly used fluorophores during qPCR. For optimal results, KAPA2G Robust HotStart ReadyMix PCR kits are recommended for downstream PCR applications.
What are the key features of the KAPA Express Extract system?
How many PCR reactions can be performed from a single DNA extraction reaction?
Depending on the sample type, a single extraction typically yields sufficient template DNA for 50 – 500 standard PCR reactions. Usually 1 – 2 μL of the extracted supernatant is used in a PCR reaction (50 – 100 PCRs). To determine how many PCR reactions can be achieved from a single extraction, prepare a serial dilution with TE or Tris pH 8.0 with a small volume of extracted sample. With each serial dilution, perform a PCR to determine the optimal dilution factor.
What sample types have successfully been extracted with KAPA Express Extract Kits and amplified reliably with KAPA2G Robust HotStart ReadyMix?
What sample types are not recommended for use with KAPA Express Extract Kits?
What are the key areas of optimization?
KAPA Express Extract Kits have been extensively tested for the extraction of DNA from a wide range of sample types. Depending on the sample type, various DNA damaging agents and/or inhibitors are likely to be present that can affect both the extraction process and the downstream PCR. Initially, optimize the PCR protocol using the following recommendations and then repeat the DNA extraction.
Is centrifugation a requirement prior to PCR?
Depending on the sample type it is possible to omit the centrifugation step after the extraction reaction. KAPA2G Robust DNA Polymerase is recommended for downstream PCR since sample debris and inhibitors will be present at a higher concentration and will almost always result in unreliable results if other DNA polymerases such as wild-type Taq are used. Pelleting the debris will result in a more reliable PCR. It is essential to pellet blood prior to use in downstream applications.
Can the DNA extracted using the KAPA Express Extract Kit be used directly in a qPCR?
DNA extracted using KAPA Express Extract Kits can be used directly in qPCR, however there are limitations. Primary limitations include: quenching of the fluorophore by carryover inhibitors (e.g. blood) is well known to quench SYBR fluorescence; inhibition of the qPCR reaction; and/or low concentrations of DNA from extraction protocol.
Recommendations for using KAPA Express Extract with downstream qPCR include:
What are the storage recommendations for the KAPA Express Extract Kit?
Upon receipt, store the entire kit at -20°C in a constant-temperature freezer. When stored under these conditions and handled correctly, all kit components will retain full activity for at least six months from the date of receipt, or until the expiry date indicated on the kit. KAPA Express Extract Buffer and enzyme may be stored at 4°C for regular, short-term use (up to one week). Provided that it has been handled carefully and not contaminated, the kit components are not expected to be compromised if left (unintentionally) at room temperature for short periods of time (up to 24 hours). Long-term storage at room temperature or 4°C is not recommended. Please note that reagents stored above -20°C are more prone to degradation when contaminated by the user; storage at such temperatures is therefore at the user’s own risk.
How long can extracted DNA be stored?
DNA extracted using the KAPA Express Extract Kit will degrade over time in 1X Express Extract Buffer and the presence of carryover inhibitors may increase the degradation process. Typically DNA extracted from “clean” samples such as buccal swabs and hair follicles are stable at 4°C or -20°C for several weeks after extraction, but this can be reduced to days depending on the sample type. A 1:5 dilution of the DNA extract in TE Buffer is recommended for long-term storage. This is done to ensure that the DNA is stored in a stable buffered environment. The dilution factor may be varied between 1:1 and 1:20, depending on the downstream application and yield of DNA. For downstream applications that are sensitive to EDTA, TE may be replaced with 10 mM Tris-HCl, pH 8.0 – 8.5. DNA extracts stored in this manner are typically stable for at least six months. For longer-term storage (especially from samples with a high concentration of carryover inhibitors) it is recommended that the DNA be further purified using an isopropanol or ethanol precipitation to totally remove inhibitors.
Can I use other manufacturers of Taq Polymerase with DNA extracted using the KAPA Express Extract Kit?
Wild-type Taq Polymerase will work with DNA extracted from “clean” sample types (e.g., buccal swabs, hair follicles) but will be unreliable when amplifying more challenging samples and templates. For the highest performance amplification, the use of KAPA2G Robust HotStart ReadyMix is recommended for all sample types.
Can the DNA extracted with the KAPA Express Extract Kit be used with other products from Kapa Biosystems?
KAPA Taq DNA Polymerase, KAPA2G Fast DNA Polymerase, KAPA HiFi DNA Polymerase, and KAPA SYBR FAST qPCR Kits have all successfully been used with DNA extracted using KAPA Express Extract to amplify a range of amplicons. KAPA2G Robust DNA Polymerase is recommended for everyday use with DNA extracted with KAPA Express Extract due to improved performance in the presence of carryover inhibitors.
Is a xylene wash step still required when working with FFPE tissue?
A xylene wash step is not required when using the KAPA Express Extract Kit. After the centrifugation step, the layer of wax is usually found on top of the buffer or on the side. The supernatant contains the DNA and is retrieved by puncturing through the wax layer on top. It is recommended to trim the excess wax around the sample using a sterile scalpel to leave only the tissue. Excess wax will not affect the extraction process, but will make it more difficult to recover the DNA.
Can the KAPA Express Extract Kit be used for RNA extraction?
The extraction process has been optimized for DNA. RNA will chemically degrade during the heating protocol and RNA extraction is not recommended with the KAPA Express Extract Kit.