Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Normalization of reverse transcription quantitative-PCR with housekeeping genes in rice.

Biotechnology letters - 1 Nov 2003

Kim Bo-Ra, Nam Hee-Young, Kim Soo-Un, Kim Su-Il, Chang Yung-Jin

Abstract excerpt

Reverse transcription followed by real-time quantitative polymerase chain reaction (RT Q-PCR) is useful for the systematic measurement of plant physiological changes in gene expression. The validity of using 18S rRNA and three housekeeping genes, glyceraldehyde-3-phosphate dehydrogenase, actin, and tubulin, was tested as a reference of RT Q-PCR. Under various growth stages of etiolated seedlings, different...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Actins
Share to Korea
Share to Oryza

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Plant Proteins

Share to Reference Values

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to RNA, Ribosomal, 18S

Share to Tubulin

Source

Identifiers

PMID: 14677714
DOI: 10.1023/a:1026298032009

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Normalization of reverse transcription quantitative-PCR with housekeeping genes in rice.PMID 14677714Read ↗

Evaluation of stability and validation of reference genes for RT-qPCR expression studies in rice plants under water deficit.Semantic proximity Read ↗

Selection of candidate reference genes for real-time PCR studies in lettuce under abiotic stresses.Semantic proximity Read ↗

Reference genes in real-time PCR.Semantic proximity Read ↗

Reference genes for accurate transcript normalization in citrus genotypes under different experimental conditions.Semantic proximity Read ↗

Identification of reference genes for RT-qPCR analysis in peach genotypes with contrasting chilling requirements.Semantic proximity Read ↗

Selection and validation of reference genes for RT-qPCR analysis in Litchi chinensis Sonn. pericarpSemantic proximity Read ↗

Selection of candidate housekeeping controls in tomato plants using EST data.Semantic proximity Read ↗

Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays.Semantic proximity Read ↗

Reference gene selection for qPCR analysis during somatic embryogenesis in longan treeSemantic proximity Read ↗

Selection of suitable reference genes for qRT-PCR studies during SE initial dedifferentiation in cotton of different SE capabilitySemantic proximity Read ↗

Microarray-Based Uncovering of Reference Genes for Quantitative Real-Time PCR in Potato Tuber Infected with PVYSemantic proximity Read ↗

Evaluation of Reference Genes for Expression Normalization in Psoralea Corylifolia L. under Abiotic StressSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.