RNA LA PCR Kit

RNA LA PCR Kit

Brand: Takara Bio.
In stock
SKU
RNA LA PCR Kit
Grouped product items
Product Name Size
RNA LA PCR Kit (AMV) Ver. 1
SKU: RR012A
100 Rxns
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RNA LA PCR Kit
RNA LA PCR Kit

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The RNA LA PCR Kit is designed to generate longer and more accurate RT-PCR products. The kit uses AMV RT XL as the reverse transcriptase, which allows for efficient synthesis of first-strand cDNA up to 12 kb. AMV RT XL also provides better thermostability than other reverse transcriptases, and retains its activity over a wider range of reaction temperatures. In addition, the kit uses LA Taq, which can synthesize products up to 40 kb in size with 6.5X better fidelity than Taq Polymerase. Both the reverse transcription and amplification reactions can be performed in a single tube. The components for 3'-RACE are also supplied.

Overview

  • Enables first-strand cDNA synthesis from templates up to 12 kb in length

Applications

  • Two-step RT-PCR using AMV RT XL and reverse transcriptase
  • Amplification of longer cDNA templates following reverse transcription using Takara LA Taq

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit. The RNA LA PCR Kit was used to amplify several long fragments from the dystrophin gene (6, 8, and 12 kb) from human heart mRNA. This data shows excellent performance, even on very long products. Template: Human heart mRNA. Target cDNA: Dystrophin (6, 8, 12 kb).

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1.

Barnes, W. M. PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates. Proc. Natl. Acad. Sci. U. S. A. 91, 2216–20 (1994).

Cheng, S., Chang, S. Y., Gravitt, P. & Respess, R. Long PCR. Nature 369, 684–5 (1994).

Cheng, S., Higuchi, R. & Stoneking, M. Complete mitochondrial genome amplification. Nat. Genet. 7, 350–1 (1994).

Frohman, M. A., Dush, M. K. & Martin, G. R. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. U. S. A. 85, 8998–9002 (1988).

Gyllensten, U. B. & Erlich, H. A. Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus. Proc. Natl. Acad. Sci. U. S. A. 85, 7652–6 (1988).

Kawasaki, E. S. et al. Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro. Proc. Natl. Acad. Sci. U. S. A. 85, 5698–702 (1988).

Lawyer, F. C. et al. Isolation, characterization, and expression in Escherichia coli of the DNA polymerase gene from Thermus aquaticus. J. Biol. Chem. 264, 6427–37 (1989).

Lynas, C., Cook, S. D., Laycock, K. A., Bradfield, J. W. & Maitland, N. J. Detection of latent virus mRNA in tissues using the polymerase chain reaction. J. Pathol. 157, 285–9 (1989).

Saiki, R. K. et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239, 487–91 (1988).

Scharf, S. J., Horn, G. T. & Erlich, H. A. Direct cloning and sequence analysis of enzymatically amplified genomic sequences. Science 233, 1076–8 (1986). 

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The RNA LA PCR Kit is designed to generate longer and more accurate RT-PCR products. The kit uses AMV RT XL as the reverse transcriptase, which allows for efficient synthesis of first-strand cDNA up to 12 kb. AMV RT XL also provides better thermostability than other reverse transcriptases, and retains its activity over a wider range of reaction temperatures. In addition, the kit uses LA Taq, which can synthesize products up to 40 kb in size with 6.5X better fidelity than Taq Polymerase. Both the reverse transcription and amplification reactions can be performed in a single tube. The components for 3'-RACE are also supplied.

Overview

  • Enables first-strand cDNA synthesis from templates up to 12 kb in length

Applications

  • Two-step RT-PCR using AMV RT XL and reverse transcriptase
  • Amplification of longer cDNA templates following reverse transcription using Takara LA Taq

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit

Amplification of long mRNA (approx. 12 kb) using the RNA LA PCR Kit. The RNA LA PCR Kit was used to amplify several long fragments from the dystrophin gene (6, 8, and 12 kb) from human heart mRNA. This data shows excellent performance, even on very long products. Template: Human heart mRNA. Target cDNA: Dystrophin (6, 8, 12 kb).

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1

Schematic diagram of RNA PCR using the RNA LA PCR Kit, Version 1.1.

Barnes, W. M. PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates. Proc. Natl. Acad. Sci. U. S. A. 91, 2216–20 (1994).

Cheng, S., Chang, S. Y., Gravitt, P. & Respess, R. Long PCR. Nature 369, 684–5 (1994).

Cheng, S., Higuchi, R. & Stoneking, M. Complete mitochondrial genome amplification. Nat. Genet. 7, 350–1 (1994).

Frohman, M. A., Dush, M. K. & Martin, G. R. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. U. S. A. 85, 8998–9002 (1988).

Gyllensten, U. B. & Erlich, H. A. Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus. Proc. Natl. Acad. Sci. U. S. A. 85, 7652–6 (1988).

Kawasaki, E. S. et al. Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified in vitro. Proc. Natl. Acad. Sci. U. S. A. 85, 5698–702 (1988).

Lawyer, F. C. et al. Isolation, characterization, and expression in Escherichia coli of the DNA polymerase gene from Thermus aquaticus. J. Biol. Chem. 264, 6427–37 (1989).

Lynas, C., Cook, S. D., Laycock, K. A., Bradfield, J. W. & Maitland, N. J. Detection of latent virus mRNA in tissues using the polymerase chain reaction. J. Pathol. 157, 285–9 (1989).

Saiki, R. K. et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239, 487–91 (1988).

Scharf, S. J., Horn, G. T. & Erlich, H. A. Direct cloning and sequence analysis of enzymatically amplified genomic sequences. Science 233, 1076–8 (1986). 

Write Your Own Review
You're reviewing:RNA LA PCR Kit
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