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  2. ProdFeature

ProdFeature

212 Articles
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Can I use R-Probes v2/ ZapR v2 for the removal of rRNA sequences in other cDNA synthesis workflows or with pre-synthesized double-stranded cDNA?

  • 815
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What rRNA species are not removed by the ZapR v2?

  • 392
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What is the mechanism of sequencing library construction using the SMARTer® Stranded Total RNA-Seq Kit v2 - Pico Input Mammalian?

  • 568
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What's In-Fusion's compatibility with multiple-fragment cloning?

  • 1357
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What’s the optimal length of homologous overlaps?

  • 486
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What are the considerations for the location of homologous overlaps?

  • 603
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What's the optimal incubation time for In-Fusion?

  • 502
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Is In-Fusion capable of working with site-directed mutagenesis?

  • 694
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What are the features of Takara online primer design tools?

  • 915
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What are vector linearization and purification options for In-Fusion?

  • 613
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How should I plan my In-Fusion experiment

  • 535
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Can I use In-Fusion Cloning to clone GC-rich DNA fragments?

  • 510
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Can I clone an oligonucleotide/shRNA oligonucleotide using In-Fusion Cloning?

  • 373
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Can I use In-Fusion Cloning to assemble a covalently linked linear DNA molecule?

  • 467
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Is In-Fusion Cloning compatible with vectors carrying repeated sequences?

  • 477
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Do I have to dephosphorylate the termini of a linearized vector for In-Fusion Cloning?

  • 580
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Does In-Fusion Cloning preserve the restriction site(s) used to linearize the vector?

  • 629
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Can I split the homologous 15-nt overlap between the insert and vector, or adjacent inserts?

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