| PCR Related Products |
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| U-Taq DNA Polymerase |
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| Cat. No. |
Size |
| EU-500 |
500u |
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Description
The Polymerase gene from Thermus aquaticus (strain YT1) is cloned and expressed in E. coli, then highly purified to
produce U-Taq DNA polymerase. It is used in the amplification and sequence testing of DNA through PCR. The quality of the
U-Taq DNA polymerase has been tested by the Activity Test, SDS-Page, Endonuclease Test, etc.
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Reaction Buffer (10X): 100 mM Tris-HCl, 400mM KCI, 15mM MgCl2 , pH9.0
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Dilution Buffer: 20mL Tris-HCl, 100mM KCI, 0.5 mM EDTA, 1mM DTT, 0.5% Tween 20, 0.5 % IGEPAL CA-630(pH 8.0
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Storage Buffer: 20 mM Tris-HCI, 0.5 mM EDTA, 1mM DTT, 0,5% Tween 20, 0.5% IGEPAL CA-630(pH 8.0.). Store at -20oC.
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Concentration: 5,000 units/mL.
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Involve the dNTPs mixture: The concentration of each dNTPs is 2.5 mM.
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| Taq-redTM DNA Polymerase |
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| Cat. No. |
Size |
| ER-500 |
500u |
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Description
- Taq-red DNA Polymerase is an unique blend of U-Taq DNA Polymerase with an inert red dye. It offers the same performance as Taq DNA Polymerase . Several benefits are as following:
- This red dye enables quick visual confirmation of enzyme addition and reaction mixing, which makes performance more convenient.
- After PCR amplification, samples can be removed from the reaction and loaded directly onto agarose gel without the addition of loading buffer or tracking dye. The red dye, acting as a tracking dye, migrates between bromophenol blue and xylenecyanol at about the same rate as 400~500bp fragment.
- The concentration of Taq-red is only 1unit/µl, so the enzyme can be transferred and added more accurately.
- The enzyme generates PCR products with 3'-dA overhangs, suitable for T-A cloning.
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| s-Pfu DNA Polymerase |
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| Cat. No. |
Size |
| EP-500 |
500u |
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Description
s-Pfu DNA Polymerase is a thermostable enzyme with a molecular weight of 90 kDa.
It catalyzes the polymerization of nucleotides into duplex DNA in the 5'→3' direction,
resulting in blunt-ended PCR products without 3'-dA overhangs. s-Pfu DNA Polymerase exhibits
5'→3' exonuclease (proofreading) activity that enables the polymerase to correct the
mis-incorporation of nucleotide, and lacks 5'→3' exonuclease activity. It is suitable for PCR
and primer extension reaction that requires high fidelity when the PCR fragment is relatively shorter
than 3kb.The extension rate of s-Pfu DNA Polymerase is about 600bp/min in standard condition.
The appropriate reaction temperature is 65oC~75oC, the working concentration of dNTPs is 100-300µM, the
working concentration of Mg2+ is 2~3mM, and the optimal pH is 8.1~9.1. The amount of enzyme is 1~1.5unit
for 20µl PCR reaction, while 2~3units for 50µl PCR reaction.
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| Easy-DoTM PCR PreMix |
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Description
The Easy-DoTM PCR PreMix is a pre-mixed preparation in a lyophilized format. The mix
contains U-Taq DNA polymerase, reaction buffer, dNTPs, and tracking dye for efficient
PCR amplification. For reaction set-up, all you have to do is to add templates, specific
primers and water. After PCR amplification, samples can be loaded directly onto agarose
gel without the addition of tracking dye. The PCR premix simplifies the assembly of PCR
reaction and offers advantages of time savings, convenience, consistency, and minimal risk of contamination.
Storage: Store at -20oC for one year.
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| Description and Size |
Cat. No. |
Quantity |
| Easy-DoTM PCR PreMix, 0.2ml thin wall microtube, 20µl reaction |
EQ2.2-50 |
50 tubes |
| Easy-DoTM PCR PreMix, 0.2ml thin wall microtube, 50µl reaction |
EQ5.2-50 |
50 tubes |
| Easy-DoTM PCR PreMix, 0.5ml thin wall microtube, 20µl reaction |
EQ2.5-50 |
50 tubes |
| Easy-DoTM PCR PreMix, 0.5ml thin wall microtube, 50µl reaction |
EQ5.5-50 |
50 tubes |
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| dNTPs Mix(10mM each) |
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Description
10mM dNTPs Mix is a ready-to-use solution of dATP, dCTP, dGTP and dTTP (monosodium salts)
at a concentration of 10mM each in sterile deionized water at pH7.5, whose purity is up to
99.5% (HPLC). It is free of RNase and DNase, and is suitable for any molecular biology
application that requires pure deoxynucleotides, such as PCR, DNA sequencing, cDNA synthesis
and nick translation.
Storage: Store at -20oC.
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| dNTPs in Separate Tube(100mM each) |
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Description
dNTPs in Separate Tube contains 4×0.4ml of dATP, dCTP, dGTP and dTTP
(monosodium salts) at a concentration of 100mM each in sterile deionized water at
pH7.5, whose purity is up to 99.5% (HPLC). It is free of RNase and DNase, and suitable
for any molecular biology application that requires pure deoxynucleotides, such as PCR,
DNA sequencing, cDNA synthesis and nick translation.
Storage: Store at -20oC
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| Cat. No. |
Size |
| EN-2 |
4×0.4ml |
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| PCR enhancer |
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Description
PCR enhancer can improve the efficiency of PCR amplification, increase the specificity
of PCR products, and reduce non-specific and undesirable PCR products. The recommended
amount is 1/10 of reaction volume.
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| PCR Optimizer |
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Description
GC-rich regions may form rigid secondary structure which makes difficult or
impossible for the DNA polymerases to work under standard PCR conditions.
The PCR optimizer can optimize PCR of problematic or GC-rich templates. The
recommended amount is 1/5 of reaction volume.
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Viswagen Biotech Pvt. Ltd., 23/863G, Thazhathuveettil Buildings, Market Road, Pala, Kerala 686 575; India
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Web: www.viswagen.com, Phone: +91-98-46804374; Fax: +91-4822-215075
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Contacts: customer service: customer.service@viswagen.com
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| Copyright © 2007 Viswagen Biotech Pvt. Ltd. |
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