Master mix for isothermal DNA amplification with EvaGreen
For in vitro use only!
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
Short term storage (up to 3 months) at 4 °C possible.
Shelf Life: 12 months
Concentration: 2x conc.
Spectroscopic Properties: λexc 500 nm (EvaGreen bound to DNA), λem 530 nm (EvaGreen bound to DNA)
Saphir Bst2.0 GreenMaster is a complete 2x conc. master mix for isothermal amplification of DNA. The mix is based on a genetically optimized Bst polymerase that allows rapid and speciﬁc ampliﬁcation of DNA at constant temperature (60 to 65 °C). The enzyme shows high strand displacement activity and generates an ampliﬁcation factor of up to 109 which is comparable to approx. 30 cycles in a PCR assay. LAMP technique allows detection of a target gene within 10 - 30 minutes.
Saphir Bst2.0 GreenMaster (orange cap)
Saphier Bst2.0 Polymerase, dNTPs, reaction buffer, glycerol, EvaGreen DNA intercalator dye, stabilizers
The mix contains the fluorescent DNA stain EvaGreen® that intercalates into DNA during the amplification process and allows the direct quantification of target DNA by fluorescence detection (analogous to real-time PCR).
The mix can be combined with ROX reference dye (#PCR-351) to allow a signal normalization in real-time PCR instruments that are compatible with the evaluation of the ROX signal.
Isothermal ampliﬁcation is an extremely sensitive detection method and care should be taken to avoid contamination of set-up areas and equipment with DNA of previous reactions. A problem may be ampliﬁcation in no-template controls due to carry-over contamination or ampliﬁcation of unspecifically annealed primers or primer dimer formations.
Typically, 4 different primers are used to identify 6 distinct DNA regions allowing the specific amplification of a target gene. An additional pair of primers further accelerates the amplification allowing to cut down the total detection time to 10-20 min.
The manual design of primers may be challenging due to the complex reaction sequence. To simplify the design process the use of a primer design software is recommended.
As sensitivity and non-template ampliﬁcation of in-silico designed primers may vary, the evaluation of 2 - 4 real primer sets before choosing a ﬁnal set is recommended.
A reaction volume of 20-50 μl is recommended for most applications. Pipet with sterile ﬁlter tips and perform the set-up in an area separate from DNA preparation or analysis. No-template controls should be included in all ampliﬁcations.
First, prepare a 10x conc. primer pre-mix. Second, set-up the isothermal ampliﬁcation assay:
|component||stock conc.||final conc.||20 μl||50 μl|
|Saphir Bst2.0 GreenMaster||2x||1x||10 μl||25 μl|
|Primer Mix||10x||1x||2 μl||5 μl|
|Template DNA||<500 ng/assay||x μl||x μl|
|PCR-grade Water||fill up to 20 μl||fill up to 50 μl|
If amplification in no-template controls occurs the following points should be reviewed.
Cross contamination from environments
Carry-over contamination from previous reaction products
Non-template amplification from primers