04743814001
Roche
Expand™ 20 kbPLUS PCR System, dNTPack
sufficient for ≤40 reactions, pkg of 200 U, suitable for PCR, dNTPs included
用途
sufficient for ≤40 reactions
特点
Long Range PCR
dNTPs included
hotstart: no
包装
pkg of 200 U
制造商/商品名称
Roche
储存条件
avoid repeated freeze/thaw cycles
参数
68 °C optimum reaction temp.
技术
PCR: suitable
输入
purified DNA
运输
dry ice
储存温度
−20°C (−15°C to −25°C)
一般描述
The Expand 20 kbPLUS PCR System is composed of an enzyme mix containing thermostable Taq DNA polymerase and Tgo DNA polymerase, a thermostable DNA polymerase with proofreading activity. This powerful polymerase mixture and associated buffer system is designed to give a high yield of PCR product when fragments longer than 20 kb need to be amplified.
T/A cloning can also be performed.
T/A cloning can also be performed.
The kit has control human genomic DNA and a set of control primers for amplifying a 23kb fragment. This test can be used to test template DNA and primer pair performance.
Use 3.75 U for a standard 50μL PCR.
Each dNTPack contains 10mM additive-free sodium salt nucleotides as a ready-to-use mix.
To obtain long PCR products, first evaluate length and purity of the DNA template. Handling all genomic DNA templates with care. Genomic DNA template should be larger than 50kb, as determined with agarose gel electrophoresis.
Use 3.75 U for a standard 50μL PCR.
Each dNTPack contains 10mM additive-free sodium salt nucleotides as a ready-to-use mix.
To obtain long PCR products, first evaluate length and purity of the DNA template. Handling all genomic DNA templates with care. Genomic DNA template should be larger than 50kb, as determined with agarose gel electrophoresis.
应用
Choose Expand™ 20 kbPLUS PCR System when amplifying genomic DNA fragments up to 35 kb. Expand 20 kbPLUS PCR System features a specifically optimized buffer and enzyme-blend mixture to amplify extra-long pieces of DNA (over 20 kb). Control primers and DNA produce fragments of 23 kb in length.
- PCR
- RT-PCR
- Large-fragment amplification
特点和优势
- Go the limit: The buffer and enzyme-blend amplify products over 20kb DNA.
- Easy PCR monitoring: Human genomic DNA and human control β-globin primers amplify a 23kb fragment.
- Test template quality: Control reagents also test template quality and primer pair performance.
- Cost-effective: Use the convenient premixed solution of PCR grade dNTPs.
包装
1 kit containing 7 components
制备说明
Store supplied human control DNA at 2–8 °C, all other components at -15 to -25°C.
分析说明
Each lot of Expand 20kbPLUS PCR System is function-tested in PCR using human genomic DNA and specific primers for β-globin to amplify a 23kb fragment.
其他说明
仅用于生命科学研究。不可用于诊断。
Volume Activity: 5 U/μl
法律信息
Use of this product is covered by US patent claims and corresponding patent claims outside the US. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser′s own internal research. No right under any other patent claim, no right to perform any patented method, and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser′s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patent claims require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.
Expand is a trademark of Roche
仅试剂盒组分
产品编号
说明
- Expand 20 kbPLUS Enzyme Mix
- Expand 20 kbPLUS Reaction Buffer, with 27.5 mM MgCl2 10x concentrated
- MgCl2 Stock Solution 25 mM
- Human Genomic DNA
- Human β-globin Control Primer forward, (HβG forward)
- Human β-globin Control Primer reverse, (HβG reverse)
- PCR Nucleotide Mix
危险声明
预防措施声明
危险分类
Aquatic Chronic 3
储存分类代码
12 - Non Combustible Liquids
WGK
WGK 2
闪点(°C)
does not flash
法规信息
常规特殊物品
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商品
The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.
热启动PCR的目的在于抑制PCR反应,从而减少非特异性扩增、防止引物二聚体形成并提高产物产量。
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