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GE27-9261-01

First-strand cDNA Synthesis Kit

Cytiva 27-9261-01

Synonyme(s) :

cDNA Synthesis Kit

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About This Item

Code UNSPSC :
41116006
Nomenclature NACRES :
NA.55

Fabricant/nom de marque

Cytiva 27-9261-01

Couleur

colorless

Conditions d'expédition

dry ice

Température de stockage

−20°C

Catégories apparentées

Description générale

Designed to generate full-length first-strand cDNA from mRNA templates. Following first-strand cDNA synthesis, the sample can be used directly for in vitro amplification using PCR or for second-strand synthesis using the Gubler-Hoffman method.

First-Strand cDNA Synthesis Kit is designed to generate full-length first-strand cDNA from mRNA templates. Following first-strand cDNA synthesis, the sample can be used directly for in vitro amplification using PCR or for second-strand synthesis using the Gubler-Hoffman method. Primers are not included in the preassembled First-Strand Reaction Mixes, thus allowing use of a primer of choice. Two primers are included with the kit. pd(N)6 Primer (random hexamer) is used to prepare libraries for screening with antibodies, to increase the representation of 5′-ends of mRNAs having significant secondary structure, or to copy mRNAs lacking a poly(A) tail.

The NotI-(dT)18 Bifunctional Primer can be used to prime selectively on mRNA that has a poly(A) tail. It can also be used as a PCR primer following first-strand synthesis. The NotI restriction site, located at the 5′-end of the primer, is particularly useful for subsequent directional cloning of cDNA and PCR products.

First-Strand cDNA Synthesis Kit contains the following reagents, sufficient for up to 55 first-strand syntheses, each of which will produce enough material for up to 15 amplification reactions: Bulk First-Strand cDNA Reaction Mixes, mRNA Standard, DTT Solution, RNase-Free Water, pd(N)6 Primer, NotI-(dT)18 Bifunctional Primer, and instruction booklet.

Application

First-strand cDNA synthesis kit has been used to reverse transcribe total RNA into cDNA.

Caractéristiques et avantages

  • For synthesis of single-stranded cDNA prior to amplification by PCR.
  • Features preassembled bulk reaction mixes to save time and minimize potential for pipetting errors.
  • Allows users to choose primers.
  • Includes a choice of two primers: pd(N)6 random hexamers and NotI-(dT)18.

Stockage et stabilité

Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.

Remarque sur l'analyse

To view the Certificate of Analysis for this product, please visit www.cytiva.com.

Code de la classe de stockage

12 - Non Combustible Liquids


Certificats d'analyse (COA)

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

Registered report: A coding-independent function of gene and pseudogene mRNAs regulates tumour biology
Israr Khan
eLife (2015)
Juan José Fung et al.
eLife, 4 (2015-09-04)
The Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of selected experiments from a number of high-profile papers in the field of cancer biology. The papers, which were published between 2010
Replication Study: BET bromodomain inhibition as a therapeutic strategy to target c-Myc
Fraser Aird
eLife (2017)
Dale Cowley et al.
eLife, 4 (2015-09-04)
The Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of selected experiments from a number of high-profile papers in the field of cancer biology. The papers, which were published between 2010
Denise Chroscinski et al.
eLife, 4 (2015-02-26)
The Nature in 2010 (Ricci-Vitiani et al., 2010). The experiments that will be replicated are those reported in Figure 4B and Supplementary Figure 10B (Ricci-Vitiani et al., 2010), which demonstrate that glioblastoma stem-like cells can derive into endothelial cells, and

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