Identification of an anonymous RFLP DNA probe through multiple [An article from: Bioresource Technology]
Book Details
PublisherElsevier
ISBN / ASINB000P6OCSU
ISBN-13978B000P6OCS6
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MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Bioresource Technology, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
The genome of Aspergillus niger (MPS-002) was subjected to RAPD fingerprinting using none different random oligonucleotide primers. A 0.7Kb PCR amplicon, generated by primer-3 could be used as a RFLP probe to differentiate A. niger (ATCC 16880) from A. niger (MPS-002). The probe revealed DNA polymorphism internal to two different EcoRI recognition sequences spaced apart at a distance of 0.4Kb within a 4.0Kb EcoRI fragment of the genome of both the strains. Localized genome mapping analysis further revealed that the 0.7Kb RFLP probe was positioned at a distance of 2.7Kb and 0.6Kb from the two ends of a 4.0Kb EcoRI fragment, respectively within the genome of the two strains of A. niger.
Description:
The genome of Aspergillus niger (MPS-002) was subjected to RAPD fingerprinting using none different random oligonucleotide primers. A 0.7Kb PCR amplicon, generated by primer-3 could be used as a RFLP probe to differentiate A. niger (ATCC 16880) from A. niger (MPS-002). The probe revealed DNA polymorphism internal to two different EcoRI recognition sequences spaced apart at a distance of 0.4Kb within a 4.0Kb EcoRI fragment of the genome of both the strains. Localized genome mapping analysis further revealed that the 0.7Kb RFLP probe was positioned at a distance of 2.7Kb and 0.6Kb from the two ends of a 4.0Kb EcoRI fragment, respectively within the genome of the two strains of A. niger.
