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Merck

03353621001

Roche

5′/3′ RACE Kit, 2nd Generation

sufficient for 10 reactions

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10 REACTIONS
US$ 778,00

US$ 778,00

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10 REACTIONS
US$ 778,00

About This Item

Código UNSPSC:
41106313
NACRES:
NA.55

US$ 778,00

PRECIOS SIN IMPUESTOS NACIONALES

Check Cart for Availability

uso

sufficient for 10 reactions

Nivel de calidad

fabricante / nombre comercial

Roche

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C (−15°C to −25°C)

Categorías relacionadas

Descripción general

Rapid Amplification of cDNA ends (RACE) is a prevalent technique used to rapidly obtain full-length cDNA from partially known sequences.[1] The 5′/3′ RACE kit contains Transcriptor Reverse Transcriptase and recombinant Terminal Transferase. Transcriptor Reverse Transcriptase transcribes full-length cDNA for the highly sensitive and rapid amplification of either 5′ or 3′ cDNA fragments up to 14 kb. Due to its thermostability (up to +65 °C), it can work with GC-rich templates with high secondary structure. High sensitivity can be achieved using Transcriptor Reverse Transcriptase, resulting in highly efficient cDNA synthesis and the generation of long RACE products. Recombinant Terminal transferase is used to add a homopolymeric A-tail to the 3′ end of the cDNA.[2] The poly(A)+ tail decreases the likelihood of inappropriate truncation by the oligo(dT)-anchor primer, and overcomes the weaker A/T compared to the G/C hybridization. Moreover, longer stretches of A residues are required before the oligo(dT)-anchor primer can hybridize to an internal site and can truncate the amplification product. Tailed cDNA is amplified by PCR using a gene-specific primer and the oligo(dT)-anchor primer. The obtained cDNA is further amplified by a second PCR using a nested specific primer and the PCR-anchor primer, allowing RACE products to be cloned into an appropriate vector for subsequent studies.

Especificidad

Heat inactivation: Terminal Transferase: 70 °C for 10 minutes
Transcriptor Reverse Transcriptase: 85 °C for 5 minutes

Aplicación

5′/3′ RACE Kit, 2nd Generation is suitable for
  • Structural and expression studies of RNA molecules[3]
  • Generating full-length cDNAs[4][5]
  • Isolation and characterization of 5′ or 3′ ends from low-copy RNA messages[6]
  • first strand cDNA synthesis[6]
  • Amplification and further cloning of rare mRNAs[6]
  • Use in conjunction with exon-trapping methods
  • Products of the RACE reaction can be directly sequenced without cloning

Características y beneficios

  • Robust performance: Recombinant Transcriptor Reverse Transcriptase allows procession through regions of difficult secondary RNA structure.
  • Convenient: Function and expression studies of either 5′ or 3′ end of the RNA can be performed with the same kit.
  • Reliable: dA tailing of cDNA with Recombinant Terminal Transferase decreases the likelihood of inappropriate truncation.
  • Reproducible: Oligo dT-anchor primer with non 3′dT ensures correct binding to the inner end of the poly (A) tail.
  • Produce long fragments: Generate cDNA up to 14kb in length with Transcriptor Reverse Transcriptase.
The control reaction includes transcription of the control RNA into first-strand cDNA using the control primer neo1/rev. Amplification of the cDNA is performed using the control primer neo2/rev and neo3/for to obtain a 157-bp PCR product. Tailing of the purified cDNA is performed with dATP. Amplification of the tailed cDNA is performed with oligo dT-anchor primer and the control primer neo2/rev to obtain a 293-bp PCR product.

Envase

1 kit containing 12 components

Otras notas

For life science research only. Not for use in diagnostic procedures.

Solo componentes del kit

Referencia del producto
Descripción

  • cDNA Synthesis Buffer 5x concentrated

  • Transcriptor Reverse Transcriptase 20 U/μl

  • Deoxynucleotide Mix

  • dATP, pH 7.5 (20 °C)

  • Reaction Buffer 10x concentrated

  • Terminal Transferase, recombinant

  • Control neo-RNA 1 ng/μl

  • Oligo dT-Anchor Primer

  • PCR Anchor Primer

  • Control Primer neo1/rev primer 12.5 μM

  • Control Primer neo2/rev primer 12.5 μM

  • Control Primer neo3/for primer 12.5 μM

Ver todo (12)

Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

does not flash

Punto de inflamabilidad (°C)

does not flash


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Reverse transcriptase adds nontemplated nucleotides to cDNAs during 5'-RACE and primer extension
Chen D and Patton JT
Biotechniques, 30(3), 574-582 (2018)
Charles-Peter Xavier et al.
Journal of molecular biology, 393(2), 287-299 (2009-08-05)
Coronin 1C (synonyms: coronin-3, CRN2), a WD40 repeat-containing protein involved in cellular actin dynamics, is ubiquitously expressed in human tissues. Here, we report on the identification and functional characterization of two novel coronin 1C isoforms, referred to as CRN2i2 and
Florian Dunker et al.
eLife, 9 (2020-05-23)
The exchange of small RNAs (sRNAs) between hosts and pathogens can lead to gene silencing in the recipient organism, a mechanism termed cross-kingdom RNAi (ck-RNAi). While fungal sRNAs promoting virulence are established, the significance of ck-RNAi in distinct plant pathogens
Oladapo Yeku et al.
Methods in molecular biology (Clifton, N.J.), 703, 107-122 (2010-12-03)
Rapid Amplification of cDNA ends (RACE) provides an inexpensive and powerful tool to quickly obtain full-length cDNA when the sequence is only partially known. Starting with an mRNA mixture, gene-specific primers generated from the known regions of the gene and
Nature methods, 2(8), 629-630 (2005-09-09)
This method is used to extend partial cDNA clones by amplifying the 5' sequences of the corresponding mRNAs 1-3. The technique requires knowledge of only a small region of sequence within the partial cDNA clone. During PCR, the thermostable DNA

Artículos

In addition to the troubleshooting provided in the product manual, most probably the efficiency of the tailing reaction performed by Terminal Transferase could be impaired. This could occur due to several reasons (which will not only affect the control reaction, but 5′ RACE in general):

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