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PCR Primer Design (Record no. 5914)

MARC details
000 -LEADER
fixed length control field 04068nam a22004575i 4500
001 - CONTROL NUMBER
control field 978-1-0716-1799-1
003 - CONTROL NUMBER IDENTIFIER
control field DE-He213
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260610083637.0
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr nn 008mamaa
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 211113s2022 xxu| s |||| 0|eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781071617991
-- 978-1-0716-1799-1
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/978-1-0716-1799-1
Source of number or code doi
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number RB155-155.8
072 #7 - SUBJECT CATEGORY CODE
Subject category code MFN
Source bicssc
072 #7 - SUBJECT CATEGORY CODE
Subject category code MED107000
Source bisacsh
072 #7 - SUBJECT CATEGORY CODE
Subject category code MFN
Source thema
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 616.042
Edition information 23
245 10 - TITLE STATEMENT
Title PCR Primer Design
Medium [electronic resource] /
Statement of responsibility, etc. edited by Chhandak Basu.
250 ## - EDITION STATEMENT
Edition statement 3rd ed. 2022.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture New York, NY :
Name of producer, publisher, distributor, manufacturer Springer US :
-- Imprint: Humana,
Date of production, publication, distribution, manufacture, or copyright notice 2022.
300 ## - online resource
Extent XIII, 276 p. 90 illus.
Other physical details online resource.
336 ## - CONTENT TYPE
Content type term text
Content type code txt
Source rdacontent
337 ## - MEDIA TYPE
Media type term computer
Media type code c
Source rdamedia
338 ## - CARRIER TYPE
Carrier type term online resource
Carrier type code cr
Source rdacarrier
347 ## - DIGITAL FILE CHARACTERISTICS
File type text file
Encoding format PDF
Source rda
490 1# - SERIES STATEMENT
Series statement Methods in Molecular Biology,
International Standard Serial Number 1940-6029 ;
Volume/sequential designation 2392
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note The significance of PCR primer design in genetic diversity studies; exemplified by recent research into the genetic structure of marine species -- Enhancing cohort PASA efficiency from lessons assimilated by mutant genotyping in C. elegans -- Design of oligonucleotides for allele-specific amplification based on PCR and isothermal techniques -- Detection of rubella virus by tri-primer RT-PCR assay and genotyping by fragment RT-PCR -- Design of mismatch primers to identify and differentiate closely related (sub)species – application to the authentication of meat products -- Primer design for the analysis of closely related species – application of non-coding mtDNA and cpDNA sequences -- Designing PCR primers for the amplification-refractory mutation system -- Validation of circular RNAs by PCR -- Primer Designing for Amplifying an AT-Rich Promoter from Arabidopsis thaliana -- PLASmid TAXonomic PCR (PlasTax-PCR), a multiplex relaxase MOB typing to assort plasmids into taxonomic units -- Multiplex PCR Design for Scalable Resequencing -- Identification of gene copy number in the transgenic plants by quantitative polymerase chain reaction (qPCR) -- qPrimerDB: A powerful and user-friendly database for qPCR primer design -- PCR primer design for the rapidly evolving SARS-CoV-2 genome -- Universal primers for detection of novel plant capsid-less viruses: Papaya umbra-like viruses as example -- A guide to using FASTPCR software for PCR, in silico PCR, and oligonucleotide analysis -- Pyrosequencing Primer Design for Forensic Biology Applications.-Phosphate‌ ‌methylated‌ ‌oligonucleotides‌ ‌as‌ ‌a‌ ‌novel‌ ‌primer‌ ‌for‌ ‌PCR‌ ‌and‌ ‌RT-PCR‌. .
520 ## - SUMMARY, ETC.
Summary, etc. This third edition provides new and updated chapters on design PCR primers for successful DNA amplification. Chapters are divided into seven parts, including primer design strategies for quantitative PCR, genotyping, multiplex PCR, in silico PCR primer design, and primer design to identify plant and animal viruses. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Authoritative and easily accessible, PCR Primer Design, Third Edition aims to be useful for various fields of molecular biology, including biotechnology, molecular genetics, and recombinant DNA technology.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medical genetics.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Medical Genetics.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Basu, Chhandak.
Relator term editor.
Relationship edt
-- http://id.loc.gov/vocabulary/relators/edt
710 2# - ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element SpringerLink (Online service)
773 0# - HOST ITEM ENTRY
Title Springer Nature eBook
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Printed edition:
International Standard Book Number 9781071617984
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Printed edition:
International Standard Book Number 9781071618004
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Printed edition:
International Standard Book Number 9781071618011
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title Methods in Molecular Biology,
International Standard Serial Number 1940-6029 ;
Volume/sequential designation 2392
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/978-1-0716-1799-1">https://doi.org/10.1007/978-1-0716-1799-1</a>
912 ## -
-- ZDB-2-PRO

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