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CopyRight® v2.0 BAC Cloning Kit
BAC文库构建试剂盒,BAC 克隆试剂盒,大片段BAC文库
CopyRight® v2.0 BAC Cloning Kits (pSMART® BAC and pEZ™ BAC)
· 有效克隆任何大小在200kb的片段
· 从A/T或G/C丰富的基因组创建文库
· 高插入稳定性
· 诱导拷贝数
Lucigen's CopyRight® v2.0 BAC克隆试剂盒带有pSMART® BAC (Figure1)或pEZ BAC (Figure 2) 载体和适用于BAC文库优化的感受态细胞,确保文库的准确性,可靠性和有效性。这些载体整合了CloneSmart®无转录技术,最小化克隆的偏好性,有利于克隆产毒素基因。随着诱导拷贝数的扩增(20到50倍)可获得更高的DNA量。LacZ-sacB片段可以消除未切割载体所形成的假阳性克隆。不像其他BAC克隆系统,Lucigen's CloneSmart技术确保了未克隆化的插入也能稳定遗传。在克隆过程中,序列不容易发生丢失或重排。CopyRigh盒子与其他同类盒子相比,以较好的价格保证了最优的BAC克隆。图3显示了一个用pSMART BAC 载体构建的随机剪切的BAC文库。
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| Figure 1. CopyRight vector pSMART BAC. |
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| Figure 2. CopyRight vector pEZ BAC. |
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| Figure 3. 用pSMART BAC载体构建的拟南芥的随机剪切BAC文库. |
易于成功
有效的获得克隆或创建文库。the CopyRight v2.0克隆盒子消除了繁琐的载体和感受态细胞制备过程,也省去了QC试验的耗时。盒子包括最优化的试剂,连接用载体,高效感受态细胞,详细说明书和疑惑解答。
每一个CopyRight® v2.0 BAC克隆盒子都包括:切割载体(pSMART BAC带有BamHI 或HindIII位点),CopyRight DNA连接酶,CopyRight 5X连接buffer,阳性对照插入DNA,测序引物,BAC优化的Replicator v2.0电转感受态细胞(一管可做两次转化),复苏培养基,阿拉伯糖诱导溶液和操作手册。
每一个CopyRight pEZ BAC克隆盒子含有: 切割CopyRight载体(pEZ BAC 平端)CloneSmart DNA连接酶,CloneDirect™10 X连接buffer(包括ATP),阳性对照插入DNA,拷贝诱导溶液,测序引物和操作手册。盒子所带细胞还包括诱导BAC最适的Replicator v2.0感受态细胞(>1 × 1010 cfu/µg DNA),每管可做两次转化,阳性对照质粒和复苏培养基。
相关产品货号:
| Product Description |
Size |
Cat. No. |
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| BAC-Optimized Replicator v2.0 Electrocompetent Cells |
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12 rxns (DUOs) |
60210-1 |
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24 rxns (DUOs) |
60210-2 |
| CopyRight v2.0 BAC Cloning Kit, pSMART BAC BamHI w/BAC-Optimized Replicator v2.0 Electrocompetent Cells |
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10 rxns |
42030-1 |
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|
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20 rxns |
42030-2 |
| CopyRight v2.0 BAC Cloning Kit, pSMART BAC HindIII w/BAC-Optimized Replicator v2.0 Electrocompetent Cells |
|
10 rxns |
42032-1 |
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20 rxns |
42032-2 |
| CopyRight v2.0 pEZ BAC Blunt Cloning Kit w/Electrocompetent Cells |
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10 rxns |
42009-1 |
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20 rxns |
42009-2 |
| CopyRight v2.0 pEZ BAC Blunt Cloning Kit without cells |
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10 rxns |
42016-1 |
Cloning Kits & Vectors
Lucigen has a wide variety of cloning systems, including novel transcription-free cloning vectors, that improve cloning yields, reduce cloning bias, and improve sequencing throughput. For cloning the most difficult sequences, the BigEasy® v2.0 Linear Cloning System offers unmatched stability. Most Lucigen cloning vectors are pre-cut, dephosphorylated, and ready-to-use.
Go directly to Vector Sequences >
Also see Protein Expression >
General Cloning
CloneSmart® Cloning Kits (pSMART® Vectors) » Stably clone any insert in transcription-free, blunt vectors for general cloning. Choice of antibiotic resistance and copy number.
GC Cloning and Amplification (pGC™ Blue Vector) » Clone PCR products with optional blue/white screening; includes T7 & SP6 RNA polymerase promoters.
Difficult Cloning or BAC/Fosmid Cloning
BigEasy® v2.0 Linear Cloning System (pJAZZ® Vectors) » Clone the unclonable, including large or highly repetitive DNA, solely available from Lucigen.
CopyControl™ Fosmid Library Production Kits » Efficiently clone any insert up to 40 kb with a complete kit, including packaging extracts.
MaxPlax™ Lambda Packaging Extracts » Package fosmid, cosmid or lambda DNA to generate genomic libraries.
CopyRight® v2.0 BAC Cloning Kits (pSMART® BAC and pEZ™ BAC) » Efficiently clone any insert 200kb.
CopyRight® v2.0 Fosmid Cloning Kits (pSMART® FOS) » Efficiently clone any insert 35-45kb.
其他克隆相关试剂盒:
DNATerminator® End Repair Kit » Repair sheared or restriction-digested DNA to create blunt, 5' phosphorylated ends.
CloneDirect™ Rapid Ligation Kit » Proceed from ligation reaction to transformation in minutes.
Gel-Ready™ DNA Ladders » Bench-top stable markers — always ready to use.
End-It™ DNA End-Repair Kit » Prepare blunt, phosphorylated DNA ends from PCR product or sheared DNA.
GELase™ Agarose Gel-Digesting Preparation » Recover DNA and RNA from low-melting point agarose gels.
Fast-Link™ DNA Ligation Kit » Ligate DNA for cloning applications.
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文献和实验Sequencing of BAC DNA--BAC DNA测序
16 µl BigDye Terminator Ready Reaction Mix 1 µg BAC DNA (determined from gel) 10 pmol primer water to 40 µl Heat tubes at 95℃ for 5 min., then perform 30 cycles of: 95℃ x 30 sec 55℃ x 10 sec 60℃ x 4 min Run BACs on a 377 and load the entire
genome sequencing. BACs are easily purified as plasmid DNAs, have little if any chimerism, and are stable, with a very few interesting exceptions. Both BAC and bacteriophage P1-derived artificial chromosome (PAC) cloning systems have been developed
-free BAC DNA (3 ), or endotoxin-free BAC DNA (4 ). Cloning, library construction, DNA labeling, sequencing, fingerprinting, transfection, and DNA microarray are examples of downstream applications, which are described in the following chapters.
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