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Cited by 283

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

PCR-based cDNA library construction: general cDNA libraries at the level of a few cells

Open access
Belyavsky, A., Vinogradova, T., Rajewsky, K.·1989·Nucleic Acids Research

Abstract

A procedure for the construction of general cDNA libraries is described which is based on the amplification of total cDNA in vitro. The first cDNA strand is synthesized from total RNA using an oligo(dT)-containing primer. After oligo(dG) tailing the total cDNA is amplified by PCR using two primers complementary to oligo(dA) and oligo(dG) ends of the cDNA. For insertion of the cDNA into a vector a controlled trimming of the 3' ends of the cDNA by Klenow enzyme was used. Starting from 10 J558L micron3 myeloma cells, total cDNA was synthesized and amplified approximately 10(5) fold. A library containing 10(6) clones was established from 1/6 of the amplified cDNA. Screening of the library with probes for three genes expressed in these cells revealed a number of corresponding clones in each case. The longest obtained clones contained inserts of 1.5 kb length. No sequences originating from carriers or from rRNA was found in 14 randomly picked clones.

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Metadata

Authors
Belyavsky, A., Vinogradova, T., & Rajewsky, K.
Venue
Nucleic Acids Research
Published
1989
Volume
17
Issue
8
Pages
2919-2932
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2033792606
Cited by
283
References
3
FWCI
7.81
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: PCR-based cDNA library construction: general cDNA libraries at the level of a few cells. https://app.cochat.ai/papers/10.1093/nar/17.8.2919
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Belyavsky, A., Vinogradova, T., & Rajewsky, K. (1989). PCR-based cDNA library construction: general cDNA libraries at the level of a few cells. Nucleic Acids Research. https://doi.org/10.1093/nar/17.8.2919

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