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NGS Library Prep kits

Molecular Research

Drug Discovery

PCR

56.00
Article number:
P520-01/02/03
56.00
Article number:
P520-01/02/03
Number of views:
1000
Keywords:
56.00
Article number:
p510-01/02/03
56.00
Article number:
p510-01/02/03
Number of views:
1000
Keywords:
55.00
Article number:
P033-01/P034-01/P035-01/P036-01
55.00
Article number:
P033-01/P034-01/P035-01/P036-01
Number of views:
1569
Keywords:
56.00
Article number:
P525-01/02/03
Phanta® Max has added unique elongation factors, specificity promoting factors and plateau uninhibiting factors, which greatly improves the ability of long fragment amplification, amplification specificity and amplification yield. Using simple templates such as λDNA and plasmids, Phanta® Max can effectively amplify fragments up to 40 kb; using complex templates such as genomic DNA, Phanta® Max can effectively amplify fragments up to 20 kb; using cDNA templates, Phanta® Max It can effectively amplify fragments up to 10 kb. Its amplification mismatch rate is 1/53 of that of ordinary Taq polymerase and 1/6 of that of Pfu polymerase. In addition, Phanta® Max has good resistance to PCR inhibitors and can be used for direct PCR of bacteria, fungi, plant tissues, animal tissues or whole blood samples. Phanta® Max contains two monoclonal antibodies that can inhibit its 5’ → 3’ polymerase activity and 3’ → 5’ exonuclease activity at room temperature, enabling highly specific hot-start PCR. This product contains Phanta® Max Super-Fidelity DNA Polymerase, dNTP and an optimized buffer system. It only needs to add primers and templates to perform amplification, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added to the system allows the 2 × Master mix to maintain stable activity after repeated freezing and thawing; the system contains an electrophoresis indicator, which can be directly spotted for electrophoresis after the PCR reaction is completed. The enzyme has 5'→ 3'polymerase activity and 3'→ 5'exonuclease activity, and the amplified product is blunt-ended, suitable for ClonExpress® and topological cloning kits (C112/C113/C115/C601).   Ultra-high fidelity: The fidelity is 53 times that of Taq DNA Polymerase and 6 times that of Pfu DNA Polymerase. For every 300,000 bases amplified, there are fewer than 5 mismatches Faster amplification: the limit speed can reach 0.5 sec/kb, 30 sec/kb can efficiently amplify most fragments Longer amplification: the effective amplification length of simple templates such as plasmid and λ DNA can reach 40 kb, the effective amplification length of genome can reach 20 kb, and the effective amplification length of cDNA can reach 10 kb. Wide adaptability: It is suitable for the amplification of various GC content fragments, has super tolerance to PCR inhibitors, and can be used for direct PCR of a variety of samples Simple operation: Dye premix, minimize experimental steps    -Store at 20°C  
56.00
Article number:
P525-01/02/03
Number of views:
4911
Keywords:
dye
and
the
of
can
amplification
to
phanta
max
dna
9999.00
Article number:
P115-01/02
This product contains 3G Taq DNA Polymerase, dNTP, visual red dye and optimized buffer system. It is easy to use, reduces pollution, and improves detection throughput and results reproducibility. 3G Taq DNA Polymerase has higher inhibitor tolerance and amplification efficiency than wild-type Taq DNA Polymerase. This product has been added with a visual red dye, which can be directly used for polyacrylamide gel electrophoresis and agarose gel electrophoresis after the reaction, which is easy to operate.   Bright: Contains visual red dye, the color is eye-catching after reaction, suitable for high-throughput detection; Convenience: The product is 2 × ready-to-use Mix, which reduces pipetting operations and is easy to use; Excellent amplification performance: 3G Taq DNA Polymerase has higher inhibitor tolerance and amplification efficiency, which improves the success rate of experiments.    Store at -30 ~ -15℃
9999.00
Article number:
P115-01/02
Number of views:
2977
Keywords:
red
and
is
dna
which
taq
the
3g
visual
9999.00
Article number:
S103-01
This kit uses a DNA polymerase with extremely high fidelity and an optimized reaction system to quickly amplify plasmids from bacterial liquid or colonies to obtain DNA that can be used for sequencing reactions. Using this kit to prepare plasmid DNA for sequencing reactions can save a lot of shaking time and cost, simplify the sample preparation process, and accelerate the speed from sample receipt to result output. Under normal circumstances, each reaction can produce 1.5-2.5 µg of plasmid DNA. The product DNA can be used directly in the sequencing reaction.   Rapid amplification of plasmids, directly used in sequencing reactions; Save shaking time and cost, simplify sample preparation process    Store at -20℃, except for Enzyme Mix v2, the rest can be stored at 4℃ for 2 weeks after defrosting
9999.00
Article number:
S103-01
Number of views:
2151
Keywords:
amplification
can
the
sequencing
dna
for
and
to
used
be
48.00
Article number:
P312-01/02/03
Vazyme LAmp® DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity). The fidelity is Taq DNA 6 times that of Polymerase. With a specially optimized buffer system, Vazyme LAmp® DNA Polymerase is very suitable for the amplification of long fragments. It can amplify fragments up to 21kb from the genome, and has high amplification efficiency for templates of different sources and different lengths. This product contains Vazyme LAmp® DNAPolymerase, dNTP and an optimized buffer system. It can be amplified by adding primers and templates, which reduces pipetting operations and improves throughput and results reproducibility. The protective agent added to the system allows Master Mix to maintain stable activity after repeated freezing and thawing. This product also provides a version containing electrophoresis buffer and dye, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113).    Efficient amplification of genome and cDNA fragments >20 kb; Very high amplification sensitivity and strong tolerance to low purity templates; Broad GC adaptability; Provide ready-to-use premix to minimize experimental steps   Store at -20°C
48.00
Article number:
P312-01/02/03
Number of views:
3789
Keywords:
dye
and
the
to
is
of
dna
amplification
which
can
47.00
Article number:
P311-01/02/03
2×VazymeLamp®MasterMix  长距离PCR的明灯  高效扩增>20kb的基因组、cDNA片段极高的扩增灵敏度,对于低纯度模板具有很强的耐受度广泛的GC适应性 提供即用型的预混液,最大程度地减少实验步骤   图一极高的扩增性能以10ng不同种属的基因组DNA为模板,用VazymeLAmp® DNAPolymerase扩增长度为3.6-21.0kb的目的片段。 M.DL15000Ma
47.00
Article number:
P311-01/02/03
Number of views:
2718
Keywords:
P311-01/02/03
长距离PCR的明灯
长距离PCR的明灯
28.30
Article number:
P302-d1/d2
Vazyme LAmp® DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity). The fidelity is Taq DNA 6 times that of Polymerase. With a specially optimized buffer system, Vazyme LAmp® DNA Polymerase is very suitable for the amplification of long fragments. It can amplify fragments up to 21kb from the genome, and has high amplification efficiency for templates of different sources and different lengths. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113). The attached PCR Enhancer can help the amplification of high GC content fragments.    Efficient amplification of genome and cDNA fragments >20 kb; Very high amplification sensitivity and strong tolerance to low purity templates; Broad GC adaptability; Provide ready-to-use premix to minimize experimental steps   Store at -20°C
28.30
Article number:
P302-d1/d2
Number of views:
2013
Keywords:
mg2+
the
and
of
amplification
dna
is
high
polymerase
for
28.30
Article number:
P301-d1/d2
Vazyme LAmp® DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity). The fidelity is Taq DNA 6 times that of Polymerase. With a specially optimized buffer system, Vazyme LAmp® DNA Polymerase is very suitable for the amplification of long fragments. It can amplify fragments up to 21kb from the genome, and has high amplification efficiency for templates of different sources and different lengths. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113). The attached PCR Enhancer can help the amplification of high GC content fragments.    Efficient amplification of genome and cDNA fragments >20 kb; Very high amplification sensitivity and strong tolerance to low purity templates; Broad GC adaptability; Provide ready-to-use premix to minimize experimental steps   Store at -20°C
28.30
Article number:
P301-d1/d2
Number of views:
2019
Keywords:
mg2+
the
and
of
amplification
dna
is
high
polymerase
for
26.00
Article number:
P301-01/02
Vazyme LAmp® DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity). The fidelity is Taq DNA 6 times that of Polymerase. With a specially optimized buffer system, Vazyme LAmp® DNA Polymerase is very suitable for the amplification of long fragments. It can amplify fragments up to 21kb from the genome, and has high amplification efficiency for templates of different sources and different lengths. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113). The attached PCR Enhancer can help the amplification of high GC content fragments.    Efficient amplification of genome and cDNA fragments >20 kb; Very high amplification sensitivity and strong tolerance to low purity templates; Broad GC adaptability; Provide ready-to-use premix to minimize experimental steps   Store at -20°C
26.00
Article number:
P301-01/02
Number of views:
2301
Keywords:
23.20
Article number:
P412-01/02/03
This product includes AceTaq® DNA Polymerse, dNTP, and optimized buffer system. It only needs to add primers and templates to perform amplification, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added to the amplification system allows 2 × AceTaq® Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be directly cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).   With chemical modification, the enzyme activity is completely blocked below 80℃; Heat at 95℃ for 5 minutes to release the activity; Suitable for amplifying low-copy genes from complex templates (genome, cDNA); Provide ready-to-use premix to minimize experimental steps   Store at -20°C
23.20
Article number:
P412-01/02/03
Number of views:
2643
Keywords:
23.20
Article number:
P411-01/02/03
This product includes AceTaq® DNA Polymerse, dNTP, and optimized buffer system. It only needs to add primers and templates to perform amplification, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added to the amplification system allows 2 × AceTaq® Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be directly cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).   With chemical modification, the enzyme activity is completely blocked below 80℃; Heat at 95℃ for 5 minutes to release the activity; Suitable for amplifying low-copy genes from complex templates (genome, cDNA); Provide ready-to-use premix to minimize experimental steps   Store at -20°C
23.20
Article number:
P411-01/02/03
Number of views:
2615
Keywords:
45.00
Article number:
P401-d1/d2/d3
AceTaq® DNA Polymerase is a chemically modified Taq DNA Polymerase whose activity is completely blocked at room temperature to prevent non-specific amplification and primer dimers during sample preparation and reaction temperature rise. The activity is released only after heating at 95°C. Compared with antibody-based hot-start Taq enzymes, AceTaq® DNA Polymerase has a more complete and stricter activity closure; compared with existing chemically modified hot-start Taq enzymes, the activation time of AceTaq® DNA Polymerase only takes 5 minutes. Compatible with existing PCR programs. AceTaq® DNA Polymerase combined with an optimized buffer system can minimize non-specific amplification and primer dimers, bring the highest sensitivity, and is very suitable for amplifying low-copy genes from complex templates (genome, cDNA). The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® Rapid Cloning Kit (C112-C113).   With chemical modification, the enzyme activity is completely blocked below 80℃; Heat at 95℃ for 5 minutes to release the activity; Suitable for amplifying low-copy genes from complex templates (genome, cDNA); Provide ready-to-use premix to minimize experimental steps   Store at -20°C
45.00
Article number:
P401-d1/d2/d3
Number of views:
4096
Keywords:
96.00
Article number:
P122-d1/d2/d3
AceTaq® DNA Polymerase is a chemically modified Taq DNA Polymerase whose activity is completely blocked at room temperature to prevent non-specific amplification and primer dimers during sample preparation and reaction temperature rise. The activity is released only after heating at 95°C. Compared with antibody-based hot-start Taq enzymes, AceTaq® DNA Polymerase has a more complete and stricter activity closure; compared with existing chemically modified hot-start Taq enzymes, the activation time of AceTaq® DNA Polymerase only takes 5 minutes. Compatible with existing PCR programs. AceTaq® DNA Polymerase combined with an optimized buffer system can minimize non-specific amplification and primer dimers, bring the highest sensitivity, and is very suitable for amplifying low-copy genes from complex templates (genome, cDNA). The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® Rapid Cloning Kit (C112-C113).   With chemical modification, the enzyme activity is completely blocked below 80℃; Heat at 95℃ for 5 minutes to release the activity; Suitable for amplifying low-copy genes from complex templates (genome, cDNA); Provide ready-to-use premix to minimize experimental steps   Store at -20°C
96.00
Article number:
P122-d1/d2/d3
Number of views:
4040
Keywords:
87.00
Article number:
P121-01
Champagne TaqTM antibody is a monoclonal antibody against Taq DNA polymerase, which inhibits DNA polymerase activity after binding to Taq DNA polymerase. Champagne TaqTM antibody has a very high affinity with Taq DNA polymerase. It can still block the activity of Taq DNA polymerase even at 65°C, so it can effectively inhibit the non-specific annealing of primers and the non-specific amplification caused by primer dimers. Champagne TaqTM antibody only needs to be heated at 95°C for 30 seconds to completely inactivate and release Taq DNA polymerase activity. It is suitable for various hot-start PCR and QPCR reactions based on Taq DNA polymerase.   The most heat-resistant Taq enzyme monoclonal antibody provides the highest specificity; Suspended cell fermentation production brings the highest quality; Good compatibility with different brands of Taq enzymes   Store at -20°C
87.00
Article number:
P121-01
Number of views:
2196
Keywords:
288.00
Article number:
P131-w1/w2/w3
This product is a 2 × Master Mix that contains Taq DNA Polymerase, dNTP and an optimized buffer system. It only needs to add primers and templates to perform the reaction, reducing errors caused by pipetting operations, and improving throughput and results. Presentability. The optimized buffer system can effectively inhibit non-specific amplification and the generation of primer dimers. The protective agent added to the system allows Mix to maintain stable activity after repeated freezing and thawing. This product contains green dye and can be directly electrophoresed after the reaction. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C115/C601).   The template is highly adaptable and compatible with a variety of complex templates; The optimized buffer system effectively inhibits non-specific amplification; With green dye, the product can be directly electrophoresed after the reaction.    Store at -20°C, store at 4°C for two months
288.00
Article number:
P131-w1/w2/w3
Number of views:
4149
Keywords:
1200.00
Article number:
P131-01/02/03
This product is a special reagent for qPCR using SYBR® Green I chimeric fluorescence method. This product is based on the hot-start AceTaq® DNA Polymerase, combined with the optimal buffer optimized for qPCR, can effectively inhibit non-specific amplification, thereby significantly improving amplification efficiency, and is suitable for high-sensitivity qPCR reactions. This product contains the optimal concentration of SYBR® Green I for qPCR reaction detection. It is a 2×premixed reagent and is easy to use. Using this product for qPCR reaction can obtain a good standard curve in a wide quantitative area, accurately quantify and detect the target gene, with good repeatability and high reliability.   Strict hot-start enzyme: AceTaq DNA Polymerase based on chemical hot-start, providing perfect amplification specificity; Optimized reaction system: patented buffer formula, which minimizes non-specific amplification and primer dimerization without repeated optimization of conditions; Excellent amplification performance: repeatable and reliable quantitative results to meet the data requirements of high-level magazines   Store at -20℃ and avoid light
1200.00
Article number:
P131-01/02/03
Number of views:
6122
Keywords:
green
and
is
amplification
for
the
qpcr
this
product
of
210.00
Article number:
P114-01/02/03
2×TaqMasterMixforPAGE(DyePlus)  产物适合于聚丙烯酰胺凝胶电泳的DNA聚合酶  优化的缓冲体系,便于快速得到理想的扩增结果提供即用型的预混液,最大程度地减少实验步骤    本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→
210.00
Article number:
P114-01/02/03
Number of views:
2903
Keywords:
P114
产物适合于聚丙烯酰胺凝胶电泳的DNA聚合酶
210.00
Article number:
P113-01/02/03
 2 × Taq Master Mix for PAGE   This product includes Taq DNA Polymerase, dNTP and optimized buffer system. Only need to add primers and templates to perform amplification, reducing pipetting operations, improving throughput and reproducibility of results. The protective agent added to the system allows Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113). This product has been specially optimized, and the PCR product is suitable for polyacrylamide gel electrophoresis and agarose electrophoresis.   Optimized buffer system is convenient for obtaining ideal amplification results quickly; Ready-to-use premix, minimizing experimental steps   Store at -20°C
210.00
Article number:
P113-01/02/03
Number of views:
2613
Keywords:
P113
21.70
Article number:
P112-01/02/03
This product contains Taq DNA Polymerase, dNTP and optimized buffer system, only need to add primers and templates to perform amplification, reducing pipetting operations, and improving detection throughput and results reproducibility. The protective agent added to the amplification system allows 2 × Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be cloned directly into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).    Optimized buffer system is convenient for obtaining ideal amplification results quickly; Ready-to-use premix, minimizing experimental steps   Store at -20°C
21.70
Article number:
P112-01/02/03
Number of views:
11434
Keywords:
P112
21.70
Article number:
P111-01/02/03
This product contains Taq DNA Polymerase, dNTP and an optimized buffer system. It can be amplified by adding primers and templates, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added to the amplification system allows 2 × Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be cloned directly into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).   Optimized buffer system is convenient for obtaining ideal amplification results quickly; Ready-to-use premix, minimizing experimental steps   Store at -20°C
21.70
Article number:
P111-01/02/03
Number of views:
7117
Keywords:
P111
400.00
Article number:
P103-01
TaqDNAPolymeraseforPAGE  产物适合于聚丙烯酰胺凝胶电泳的DNA聚合酶  优化的缓冲体系,便于快速得到理想的扩增结果   提供即用型的预混液,最大程度地减少实验步骤   本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→3’外切酶
400.00
Article number:
P103-01
Number of views:
2162
Keywords:
P103
产物适合于聚丙烯酰胺凝胶电泳的DNA聚合酶
45.00
Article number:
P102-d1/d2/d3
TaqDNAPolymerase(Mg2+freeBuffer,withdNTP)   高纯度耐热DNA聚合酶  优化的缓冲体系,便于快速得到理想的扩增结果;提供即用型的预混液,最大程度地减少实验步骤 本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→
45.00
Article number:
P102-d1/d2/d3
Number of views:
2520
Keywords:
P102-d
高纯度耐热DNA聚合酶
26.00
Article number:
P102-01/02/03
TaqDNAPolymerase(Mg2+freeBuffer)  高纯度耐热DNA聚合酶 优化的缓冲体系,便于快速得到理想的扩增结果;提供即用型的预混液,最大程度地减少实验步骤   本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→3’聚合酶活性和5
26.00
Article number:
P102-01/02/03
Number of views:
2234
Keywords:
P102-0
高纯度耐热DNA聚合酶
45.00
Article number:
P101-d1/d2/d3
TaqDNAPolymerase(Mg2+plusBuffer,withdNTP)   高纯度耐热DNA聚合酶 优化的缓冲体系,便于快速得到理想的扩增结果提供即用型的预混液,最大程度地减少实验步骤   本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→
45.00
Article number:
P101-d1/d2/d3
Number of views:
2939
Keywords:
P101-d
Taq DNA Polymerase (Mg2+ plus Buffer
with dNTP)
26.00
Article number:
P101-01/02/03
TaqDNAPolymerase(Mg2+plusBuffer)  高纯度耐热DNA聚合酶   优化的缓冲体系,便于快速得到理想的扩增结果提供即用型的预混液,最大程度地减少实验步骤   本产品由克隆有ThermusaquaticusDNAPolymerase基因的大肠杆菌表达并经过多步纯化精制得到,不含核酸内切酶、核酸外切酶以及细菌DNA。TaqDNAPolymerase具有5’→3’聚合酶活性和
26.00
Article number:
P101-01/02/03
Number of views:
3818
Keywords:
P101-01
Taq DNA Polymerase (Mg2+ plus Buffer)
24.50
Article number:
P222-01/02/03/04
This product contains Taq DNA Polymerase, extension promoter, dNTP and optimized buffer system. The amplification speed can reach 15 sec/kb. It is suitable for rapid PCR reaction. The limit amplification speed within 1 kb can reach 1 sec/kb, which is large Save PCR reaction time. The pre-prepared 2 × Master Mix only needs to add primers and templates to perform amplification when used in PCR reactions, which reduces pipetting operations and improves detection throughput and results reproducibility. This product has excellent amplification performance and high storage stability. It is suitable for PCR amplification within 5 kb using genome as template and PCR amplification within 10 kb using plasmid and λDNA as template. The protective agent added to the amplification system allows 2 × Master Mix to maintain stable activity after repeated freezing and thawing. This product contains electrophoresis buffer and green dye. It can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3’ end, which can be directly cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114)   Fast amplification speed: 15 sec/kb, the limit amplification speed can reach 1 sec/kb within 1 kb; Convenient operation: amplification can be carried out by adding primers and templates, no operation on ice is required, and the product containing dye can be directly subjected to electrophoresis; Good stability: repeated freezing and thawing for 50 times, no significant decrease in activity    Store at -20℃; after thawing, it can be stored at 4℃ for 3 months
24.50
Article number:
P222-01/02/03/04
Number of views:
8808
Keywords:
P222-01/02/03
42.00
Article number:
P213-01/02/03
This product contains Taq Plus DNA Polymerase, dNTP and optimized buffer system, suitable for high-yield PCR reactions. Compared with ordinary PCR, it has higher fidelity, stronger amplification performance and yield. It can be used for PCR amplification within 10 kb using genome as template and PCR amplification within 15 kb using plasmid and λDNA as template . The pre-prepared 2×Taq Plus Master Mix II only needs to add primers and templates to perform amplification when used in PCR reactions, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added to the amplification system allows 2 × Taq Plus Master Mix II to maintain stable activity after repeated freezing and thawing. This product contains blue double dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3'end, which can be cloned directly into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).   Strong amplification ability: For most templates and primers, the yield is significantly improved; High visibility: The color of the sample will be clearer when the PCR reaction is completed and the sample is added by agarose gel electrophoresis; Convenient operation: amplification can be carried out by adding primers and templates, no operation on ice is required, and the product containing dye can be directly subjected to electrophoresis; Good stability: 50 times of repeated freezing and thawing, no significant decrease in activity   Store at -20°C
42.00
Article number:
P213-01/02/03
Number of views:
6466
Keywords:
42.00
Article number:
P212-01/02/03
This product contains Taq Plus DNA Polymerase, dNTP and an optimized buffer system. It can be amplified by adding primers and templates, which reduces pipetting operations and improves throughput and results reproducibility. The protective agent added to the system allows Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113).   Add 3'→5' exonuclease activity; Fidelity is 6 times that of Taq DNA Polymerase; Improve amplification yield and length; Provide ready-to-use premix to minimize experimental steps; Contains electrophoresis buffer and dye, can be directly electrophoresed after the reaction   Store at -20°C
42.00
Article number:
P212-01/02/03
Number of views:
4473
Keywords:
42.00
Article number:
P211-01/02/03
This product contains Taq Plus DNA Polymerase, dNTP and an optimized buffer system. It can be amplified by adding primers and templates, which reduces pipetting operations and improves throughput and results reproducibility. The protective agent added to the system allows Master Mix to maintain stable activity after repeated freezing and thawing. This product provides a version containing electrophoresis buffer and dyes, which can be directly electrophoresed after the reaction, which is convenient to use. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113).   Add 3'→5' exonuclease activity; Fidelity is 6 times that of Taq DNA Polymerase; Improve amplification yield and length; Ready-to-use premix, minimizing experimental steps   Store at -20°C
42.00
Article number:
P211-01/02/03
Number of views:
3823
Keywords:
32.60
Article number:
P201-d1/d2/d3
Taq Plus DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity), with the fidelity of Taq DNA Polymerase 6 times. For target fragments within 5 kb in length, Taq Plus DNA Polymerase has stronger amplification performance than Taq DNA Polymerase. In general, use Taq Plus DNA Polymerase to get a higher yield. Some fragments that cannot be amplified by Taq DNA Polymerase can be amplified normally by Taq Plus DNA Polymerase. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113).    Add 3'→5' exonuclease activity; Fidelity is 6 times that of Taq DNA Polymerase; Increase amplification yield and length   Store at -20°C
32.60
Article number:
P201-d1/d2/d3
Number of views:
1794
Keywords:
29.00
Article number:
P201-01/02/03
Taq Plus DNA Polymerase is a mixed enzyme composed of Taq DNA Polymerase and a protein containing 3’→5’ exonuclease activity (proofreading activity), with the fidelity of Taq DNA Polymerase 6 times. For target fragments within 5 kb in length, Taq Plus DNA Polymerase has stronger amplification performance than Taq DNA Polymerase. In general, use Taq Plus DNA Polymerase to get a higher yield. Some fragments that cannot be amplified by Taq DNA Polymerase can be amplified normally by Taq Plus DNA Polymerase. The PCR product has an A at the 3’ end, which can be cloned into the T vector and is suitable for ClonExpress® rapid cloning kit (C112/C113).    Add 3'→5' exonuclease activity; Fidelity is 6 times that of Taq DNA Polymerase; Improve amplification yield and length   Store at -20°C
29.00
Article number:
P201-01/02/03
Number of views:
2171
Keywords:
56.00
Article number:
P515-01/02/03
Phanta® Max Super-Fidelity DNA Polymerase is an upgraded version of Phanta® Super-Fidelity DNA Polymerase. Compared with the previous generation of products, Phanta® Max has added unique elongation factors, specificity promoting factors, and plateau uninhibitory factors, which have greatly improved the ability of long fragment amplification, amplification specificity and amplification yield. Increased. Using simple templates such as λDNA and plasmids, Phanta® Max can effectively amplify fragments up to 40 kb; using complex templates such as genomic DNA, Phanta® Max can amplify fragments up to 20 kb; using cDNA templates, Phanta® Max can Effectively amplify fragments up to 10 kb. The mismatch rate is 1/53 of that of ordinary Taq enzyme and 1/6 of that of Pfu enzyme. In addition, Phanta® Max has good resistance to PCR inhibitors and can be used for direct PCR of bacteria, fungi, plant tissues, animal tissues or whole blood samples. Phanta® Max is added with two monoclonal antibodies that can inhibit its 5’→3’ polymerase activity and 3’→5’ exonuclease activity at room temperature, enabling highly specific hot-start PCR. This product contains Phanta® Max Super-Fidelity DNA Polymerase, dNTP and an optimized buffer system. It only needs to add primers and templates to perform amplification, which reduces pipetting operations and improves detection throughput and results reproducibility. The protective agent added in the system allows 2 × Master mix to maintain stable activity after repeated freezing and thawing. The amplified product is blunt-ended and is suitable for ClonExpress® rapid cloning kit (C112/C113/C114).   Super fidelity: The fidelity is 53 times that of Taq DNA Polymerase and 6 times that of Pfu DNA Polymerase. For every 300,000 bases amplified, there are less than 5 mismatches; Amplify faster: the limit speed can reach 0.5 sec/kb, 30 sec/kb can efficiently amplify most fragments; Longer amplification: simple templates such as plasmids and lambda DNA can be amplified up to 40 kb, cDNA can be amplified up to 10 kb, and genome can be amplified up to 20 kb; Wide adaptability: It is suitable for the amplification of various GC content fragments, has super tolerance to PCR inhibitors, and can be used for direct PCR of a variety of samples.   Store at -20°C
56.00
Article number:
P515-01/02/03
Number of views:
15037
Keywords:
phanta
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dna
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is
9999.00
Article number:
P511-01/02/03
Phanta® Super-Fidelity DNA Polymerase is a new generation of ultra-fidelity DNA polymerase modified from Pfu DNA Polymerase. It has extremely high amplification efficiency and wide template adaptability, and can be used in almost all PCR reactions. With the genetic engineering modification of Pfu DNA Polymerase, the processivity of Phanta® Super-Fidelity DNA Polymerase has been greatly improved, even for very complex templates, the reaction can be completed accurately and quickly. The mismatch rate is the normal Taq 1/52 of the enzyme is 1/6 of the Pfu enzyme; and the amplification speed can reach 15 seconds/kb. The high fidelity and excellent amplification efficiency make Phanta® Super-Fidelity DNA Polymerase the first choice for high-fidelity PCR. This product contains Phanta® Super-Fidelity DNA Polymerase, dNTP and an optimized buffer system. It can be amplified by adding primers and templates, reducing pipetting operations and extracting High throughput and reproducibility of results. The protective agent added to the system allows Master Mix to maintain stable activity after repeated freezing and thawing. The amplified product is blunt-ended, suitable for ClonExpress® Rapid cloning kit (C112/C113).    The fidelity is 52 times that of Taq DNA Polymerase and 6 times that of Pfu DNA Polymerase; The amplification speed is 4-150 times that of conventional polymerase; The optimized buffer system is widely applicable to various templates; Ready-to-use premix, minimizing experimental steps   Store at -20°C
9999.00
Article number:
P511-01/02/03
Number of views:
6524
Keywords:
87.00
Article number:
P505-d1/d2/d3
87.00
Article number:
P505-d1/d2/d3
Number of views:
21569
Keywords:
9999.00
Article number:
P504-d1/d3
Phanta Super-Fidelity DNA Polymerase is a new generation of ultra-fidelity DNA polymerase modified from Pfu DNA Polymerase. It has extremely high amplification efficiency and wide template adaptability, and can be used in almost all PCR reactions. With the genetic engineering of Pfu DNA Polymerase, the processivity of Phanta Super-Fidelity DNA Polymerase has been greatly improved. Even for very complex templates, the amplification reaction can be completed accurately and quickly. Phanta EVO HS Super-Fidelity DNA Polymerase is an upgraded version of Phanta HS Super-Fidelity DNA Polymerase. Compared with the previous generation product, Phanta EVO HS has added a unique extension factor and deeply optimized the reaction system to further improve its amplification stability, fidelity and ability to amplify long fragments. Using simple templates such as lambda DNA and plasmids, Phanta EVO HS can effectively amplify fragments up to 40 kb; using complex templates such as genomic DNA, Phanta EVO HS can also effectively amplify fragments up to 20 kb. Its amplification mismatch rate is 1/100 of that of ordinary Taq polymerase and 1/12 of Pfu polymerase; and the amplification speed can reach 15 seconds/kb. In addition, Phanta EVO HS has good resistance to PCR inhibitors and can be used for bacteria, fungi, Direct PCR of plant tissue, animal tissue or whole blood samples. Strict fidelity performance and excellent amplification efficiency make Phanta EVO HS the first choice for high-fidelity PCR. Phanta EVO HS has added two monoclonal antibodies that can inhibit its 5'→3' polymerase activity and 3'→5' exonuclease activity at room temperature, enabling highly specific Hot Start PCR . The enzyme has 5'→3' polymerase activity and 3'→5' exonuclease activity, and the amplified product is blunt-ended, which is suitable for ClonExpress rapid cloning kit (C112/C113). 5 × EVO Buffer has good adaptability to PCR amplification of simple or complex templates, short fragments or long fragments. It already contains 10 mM Mg2+, you can use the MgCl2 or PCR Enhancer provided with the enzyme to optimize the reaction system.    Super fidelity: the fidelity is 53 times that of Taq DNA Polymerase and 6 times that of Pfu DNA Polymerase. Every 300,000 bases amplified, with less than 5 mismatches; Faster amplification: the limit speed can reach 0.5 sec/kb, 30 sec/kb can efficiently amplify most fragments; Longer amplification: the effective amplification length of simple templates such as plasmid and λ DNA can reach 40 kb, the effective amplification length of cDNA can reach 10 kb, and the effective amplification length of genome can reach 20 kb; Wide adaptability: It is suitable for the amplification of various GC content fragments, has super tolerance to PCR inhibitors, and can be used for direct PCR of a variety of samples.   Store at -20°C
9999.00
Article number:
P504-d1/d3
Number of views:
2562
Keywords:
600.00
Article number:
P503-d1/d3
Phanta Super-Fidelity DNA Polymerase is a new generation of ultra-fidelity DNA polymerase modified from Pfu DNA Polymerase. It has extremely high amplification efficiency and wide template adaptability, and can be used in almost all PCR reactions. With the genetic engineering of Pfu DNA Polymerase, the processivity of Phanta Super-Fidelity DNA Polymerase has been greatly improved, even for very complex templates, the amplification reaction can be completed accurately and quickly. Phanta EVO Super-Fidelity DNA Polymerase It is an upgraded version of Phanta Super-Fidelity DNA Polymerase. Compared with the previous generation product, Phanta EVO has added a unique extension factor and deeply optimized the reaction system to make its amplification stability, fidelity and long-term The amplification ability of fragments has been further improved. Using simple templates such as lambda DNA and plasmids, Phanta EVO can effectively amplify fragments up to 40 kb; using complex templates such as genomic DNA, Phanta EVO can also effectively amplify fragments up to 20 kb. Fragment. Its amplification mismatch rate is 1/100 of that of ordinary Taq polymerase and 1/12 of Pfu polymerase; and the amplification speed can reach 15 seconds/kb. In addition, Phanta®EVO is good for PCR inhibitors Resistance ability, can be used for direct PCR of bacteria, fungi, plant tissues, animal tissues or whole blood samples. Rigorous fidelity performance and excellent amplification efficiency make Phanta EVO a high-fidelity PCR Enzymes are the first choice. The enzyme has 5'→3' polymerase activity and 3'→5' exonuclease activity, and the amplified product is blunt-ended, suitable for ClonExpress rapid cloning kit (C112/C113). 5 × EVO Buffer has good adaptability for simple or complex template, short fragment or long fragment PCR amplification. It already contains 10 mM Mg2+, you can use the MgCl2 or PCR Enhancer provided with the enzyme to optimize the reaction system.    Effectively amplify 20 kb genome fragments and 40 kb plasmid fragments; The fidelity is 100 times that of Taq DNA Polymerase and 12 times that of Pfu DNA Polymerase; The amplification speed is 4-150 times that of conventional polymerase; The optimized buffer system is widely applicable to various types of templates, which is convenient for obtaining ideal amplification results quickly   Store at -20°C
600.00
Article number:
P503-d1/d3
Number of views:
3608
Keywords:

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