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First Strand cDNA Synthesis Kit for RT-PCR (AMV)

sufficient for 30 reactions (including 5 control reactions), kit of 1 (10 components), suitable for RT-PCR, hotstart: no, dNTPs included

Quality Level


sufficient for 30 reactions (including 5 control reactions)

specific activity

>50 units/μg protein


dNTPs included
hotstart: no


kit of 1 (10 components)




42 °C optimum reaction temp.


RT-PCR: suitable


purified RNA

shipped in

dry ice

storage temp.


General description

The use of AMV RT for first-strand cDNA synthesis has certain advantages. The higher thermostability of this enzyme compared to M-MuLV RT allows the reaction to be performed at +42°C, giving higher specificity and better resolution of secondary structures compared to a reaction performed at +37°C.
The First Strand cDNA Synthesis Kit is used for the synthesis of the first strand cDNA as the starting reaction for two-step RT PCR.The kit includes Reverse Transcriptase AMV for first strand synthesis, two different primers, our PCR Nucleotide Mix, and Control Neo pa RNA. PCR products that are generated by RT-PCR can be cloned using standard procedures.
The amplification of RNA requires the conversion of the RNA substrate into DNA. This is achieved through the use of a reverse transcriptase such as AMV RT (avian myeloblastis virus reverse transcriptase) or M-MuLV RT (moloney murine leukemia virus reverse transcriptase). The resulting cDNA can be used as a template for a standard PCR.
AMV RT synthesizes the new cDNA strand at site(s) determined by the type of the primer used:
  • at the 3′-end of the poly(A) mRNA when Oligo-p(dT)15is used as a primer,
  • at nonspecific points along the mRNA template when using the random primer p(dN)6, or
  • at a site determined by a sequence-specific primer.


Heat inactivation: 5 min, 95 °C
Reverse Transcriptase AMV


The First Strand cDNA Synthesis Kit for RT-PCR (AMV) is suitable for:
  • Detection of the presence or absence of RNA viruses or other RNA-containing microorganisms (in combination with PCR)
  • Quantification of mRNA for monitoring differential expression of a specific mRNA
  • First step in the "differential display of mRNA"
  • Generation of cDNA libraries with large and full-length inserts
  • Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) for reverse transcription of RNA into complementary DNA.

Features and Benefits

  • Transcribes total RNA, mRNA and viral RNA along with difficult-to-transcribe secondary RNA structures
  • Obtain cDNA transcripts up to 12 kb
  • Higher thermostability (up to 50°C) and specificity than M-MuLV Reverse Transcriptase
  • Purification of the resulting cDNA before PCR reaction is not necessary
It can be used with either sequence-specific primers, poly(dT)15 primers, or random primers, p(dN)6


1 kit containing 10 components.


In the standard cDNA synthesis assay, at least 300 ng of cDNA is synthesized (i.e., 30% yield) when 1.0 μg Neo pa RNA template is incubated with 20 μCi [α-32P]-dCTP (specific activity of 3000 Ci/mmol) for 60 minutes at +42°C.

Unit Definition

Volume Activity: 20 to 25 U/μl

Other Notes

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

Kit Components Only

Product No.

  • Reverse Transcriptase AMV

  • PCR Nucleotide Mix, pH 8.5 10 mM each

  • Reaction Buffer

  • MgCl2 Stock Solution 25 mM

  • Gelatin 0.05% (w/v)

  • Oligo-p(dT)15 , 0.02 A260 units/μl 0.8 μg/μl

  • Random Primer p(dN)6 , 0.04 A260 units/μl 1.6 μg/μl

  • RNase Inhibitor 50 U/μl

  • Control Neo pa RNA (1.0 kb in length with additional 19-base 3′-poly(A) tail) 0.2 μg/μl

  • Water, PCR Grade

See All (10)

Storage Class Code

12 - Non Combustible Liquids



Flash Point(F)

does not flash

Flash Point(C)

does not flash

Certificate of Analysis

Certificate of Origin

Quotes and Ordering

Roles of Signal Transducer Pathways in Investigation of Biopsies from Patients with Bladder Tumors
Aysegul Bayrak
Asian Pacific Journal of Cancer Prevention (2017)
Jian Han et al.
Molecular medicine reports, 18(1), 1058-1066 (2018-05-31)
Atorvastatin is a member of the statin class of drugs, which competitively inhibit the activity of 5‑hydroxy‑3‑methylglutaryl‑coenzyme A reductase. The aim of the present study was to assess whether atorvastatin may protect BV‑2 microglia and hippocampal neurons against oxygen‑glucose deprivation
Screening of Selected Soil and Endophytic Fungi for Lovostatin
Biosynthetic Genes lovE and lovF
Bhargavi SD
Microbial Biotechnology (2015)
Deniz Kanliada et al.
International journal of molecular and cellular medicine, 1(4), 217-224 (2012-10-01)
The aim of this study is to determine whether there is a role of podoplanin and glutathione S-transferases T1 (GST-T1) expression in laryngeal squamous cell carcinoma. The study was completed with 33 patients and gene expression analysis was performed by qRT-PCR.
Bita Nickkholgh et al.
Fertility and sterility, 102(2), 558-565 (2014-05-28)
To evaluate the degree of enrichment of spermatogonial stem cells (SSCs) from human testicular cell cultures by ITGA6+, HLA-/ITGA6+, GPR125+, and HLA-/GPR125+ magnetic-assisted cell sorting (MACS). Experimental basic science study. Reproductive biology laboratory. Multiple samples of cryopreserved human testicular cells


First Strand cDNA Synthesis Kit for RT-PCR (AMV) Protocol

First Strand cDNA Synthesis Kit for RT-PCR (AMV) Protocol

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