custom oligonucleotide microarrays (NimbleGen Systems GmbH)
Structured Review
![Abundance of transcripts of KD1 downstream genes. Total RNA isolated from pedicel AZs of wild-type (cv New Yorker [NY]) and TAPG4::antisense KD1 transgenic (line E) plants 4 h after flower removal (A), and freshly harvested wild-type (cv VF36) and Pts mutant (B) plants were used to determine abundance of transcripts of each gene by qRT-PCR. Abundance of tomato 26S rRNA was used as an internal control. The expression ratio of each gene from <t>microarray</t> analysis is shown above the corresponding qRT-PCR column. Different letters indicate significant differences between NY and line E or between cv VF36 and Pts at each time point (Student’s t test, P < 0.05). Results are the means of three biological replicates ± sd. *, Data representing PIN9 were absent in the microarray.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_8773/pmc04348773/pmc04348773__PP_253815_f6.jpg)
Custom Oligonucleotide Microarrays, supplied by NimbleGen Systems GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdna+microarray+analyses/pmc04348773-351-0-7?v=NimbleGen+Systems+GmbH
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "A KNOTTED1-LIKE HOMEOBOX Protein Regulates Abscission in Tomato by Modulating the Auxin Pathway 1 [OPEN] "
Article Title: A KNOTTED1-LIKE HOMEOBOX Protein Regulates Abscission in Tomato by Modulating the Auxin Pathway
Journal: Plant Physiology
doi: 10.1104/pp.114.253815
Figure Legend Snippet: Abundance of transcripts of KD1 downstream genes. Total RNA isolated from pedicel AZs of wild-type (cv New Yorker [NY]) and TAPG4::antisense KD1 transgenic (line E) plants 4 h after flower removal (A), and freshly harvested wild-type (cv VF36) and Pts mutant (B) plants were used to determine abundance of transcripts of each gene by qRT-PCR. Abundance of tomato 26S rRNA was used as an internal control. The expression ratio of each gene from microarray analysis is shown above the corresponding qRT-PCR column. Different letters indicate significant differences between NY and line E or between cv VF36 and Pts at each time point (Student’s t test, P < 0.05). Results are the means of three biological replicates ± sd. *, Data representing PIN9 were absent in the microarray.
Techniques Used: Isolation, Transgenic Assay, Mutagenesis, Quantitative RT-PCR, Control, Expressing, Microarray
