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Key Documents

03353621001

Roche

5′/3′ RACE Kit, 2nd Generation

sufficient for 10 reactions

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About This Item

Code UNSPSC :
41106313
Nomenclature NACRES :
NA.55

Utilisation

sufficient for 10 reactions

Niveau de qualité

Fabricant/nom de marque

Roche

Conditions d'expédition

dry ice

Température de stockage

−20°C (−15°C to −25°C)

Description générale

Rapid Amplification of cDNA ends (RACE) is a prevalent technique used to rapidly obtain full-length cDNA from partially known sequences. 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. 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.

Spécificité

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

Application

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

Caractéristiques et avantages

  • 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.

Conditionnement

1 kit containing 12 components

Autres remarques

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

Composants de kit seuls

Réf. du produit
Description

  • 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

Afficher tout (12)

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

does not flash

Point d'éclair (°C)

does not flash


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Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Consulter la Bibliothèque de documents

D Chen et al.
BioTechniques, 30(3), 574-580 (2001-03-17)
In determining the terminal sequences of the genomic dsRNAs of rotavirus by 5'-rapid amplification of cDNA ends (5'-RACE), it was found that most of the viral cDNAs contained extra nucleotides at their 5' termini that had not been reported before
Rapid amplification of cDNA ends (RACE)
Yeku O and Frohman MA
Methods in Molecular Biology, 107-122 (2011)
Rapid amplification of 5 [prime] complementary DNA ends (5 [prime] RACE)
Sambrook J and Russell DW
Nature methods, 2, 629-630 (2005)
Erdong Cheng et al.
Journal of virology, 86(18), 10173-10185 (2012-07-13)
Hantaviruses, similarly to other negative-strand segmented RNA viruses, initiate the synthesis of translation-competent capped mRNAs by a unique cap-snatching mechanism. Hantavirus nucleocapsid protein (N) binds to host mRNA caps and requires four nucleotides adjacent to the 5' cap for high-affinity
Pengli Bu et al.
The Journal of endocrinology, 234(2), 217-232 (2017-06-04)
Mammals share common strategies for regulating reproduction, including a conserved hypothalamic-pituitary-gonadal axis; yet, individual species exhibit differences in reproductive performance. In this report, we describe the discovery of a species-restricted homeostatic control system programming testis growth and function. Prl3c1 is

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