Quantitative PCR primer design affects quantification of dsRNA-mediated gene knockdown
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
Erscheinungsjahr der gedruckten Ausgabe des Digitalisats: 2019
- Ereignis
-
Veröffentlichung
- (wo)
-
Mainz
- (wer)
-
Johannes Gutenberg-Universität Mainz
- (wann)
-
2019
- Urheber
-
Onchuru, Thomas
Kaltenpoth, Martin
- URN
-
urn:nbn:de:hebis:77-publ-594768
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:01 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Onchuru, Thomas
- Kaltenpoth, Martin
- Johannes Gutenberg-Universität Mainz
Entstanden
- 2019
Ähnliche Objekte (12)
LSSP-PCR of Trypanosoma cruzi: how the single primer sequence affects the kDNA signature
Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines
A thermodynamic approach to PCR primer design
primerJinn: a tool for rationally designing multiplex PCR primer sets for amplicon sequencing and performing in silico PCR
Tuning PCR Specificity by Chemically Modified Primer Probes
Methylation-specific PCR: four steps in primer design
GENOMEMASKER package for designing unique genomic PCR primers
MPprimer: a program for reliable multiplex PCR primer design
Stepwise partially overlapping primer-based PCR for genome walking
Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping
The knockdown of OsVIT2 and MIT affects iron localization in rice seed
PCR and real-time PCR primers developed for detection and identification of Bifidobacterium thermophilumin faeces
LSSP-PCR of Trypanosoma cruzi: how the single primer sequence affects the kDNA signature
Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines
A thermodynamic approach to PCR primer design
primerJinn: a tool for rationally designing multiplex PCR primer sets for amplicon sequencing and performing in silico PCR
Tuning PCR Specificity by Chemically Modified Primer Probes
Methylation-specific PCR: four steps in primer design
GENOMEMASKER package for designing unique genomic PCR primers
MPprimer: a program for reliable multiplex PCR primer design
Stepwise partially overlapping primer-based PCR for genome walking
Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping
The knockdown of OsVIT2 and MIT affects iron localization in rice seed
PCR and real-time PCR primers developed for detection and identification of Bifidobacterium thermophilumin faeces
LSSP-PCR of Trypanosoma cruzi: how the single primer sequence affects the kDNA signature
Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines
A thermodynamic approach to PCR primer design
primerJinn: a tool for rationally designing multiplex PCR primer sets for amplicon sequencing and performing in silico PCR
Tuning PCR Specificity by Chemically Modified Primer Probes
Methylation-specific PCR: four steps in primer design
GENOMEMASKER package for designing unique genomic PCR primers
MPprimer: a program for reliable multiplex PCR primer design
Stepwise partially overlapping primer-based PCR for genome walking
Universal probe-based intermediate primer-triggered qPCR (UPIP-qPCR) for SNP genotyping
The knockdown of OsVIT2 and MIT affects iron localization in rice seed