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4x44k microarray for japanese medaka (Genotypic Technology Pvt Ltd)

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Genotypic Technology Pvt Ltd 4x44k microarray for japanese medaka
4x44k Microarray For Japanese Medaka, supplied by Genotypic Technology Pvt Ltd, 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/custom+microarray+design+services/custom+made+4x+44k+microarray+slides+specially+designed+for+silkworm+b++mori+by+genotypic+private/pm32470873-93-5-8
Average 90 stars, based on 1 article reviews

4x44k microarray for japanese medaka - by Bioz Stars, 2026-11

90/100 stars

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Article Title: Transcriptional responses in newly-hatched Japanese medaka (Oryzias latipes) associated with developmental malformations following diluted bitumen exposure.
Article Snippet: .. A custom-designed 4x44K microarray for Japanese medaka from Genotypic Technology (Bangalore, India) was created with 23,382 probes (1417 spike-in controls, 100 duplicate probes; Table SB2; Agilent Technologies, Mississauga, ON). .. Samples were prepared by One-Color Low Input Quick Amp Gene Expression Labeling Kits (Agilent Technologies, Mississauga, ON).

Article Title: Genome-wide identification, characterization of sugar transporter genes in the silkworm Bombyx mori and role in Bombyx mori nucleopolyhedrovirus (BmNPV) infection.
Article Snippet: Genome – wide identification, characterization of sugar transporters genes in the silkworm Bombyx mori and role in Bombyx mori nucleopolyhedrovirus (BmNPV) infection Lekha Govindaraj, Tania Gupta, Vijaya Gowri Esvaran, Aravind Kumar Awasthi, Kangayam M. Ponnuvel PII: S0378-1119(15)01569-3 DOI: doi: 10.1016/j.gene.2015.12.057 Reference: GENE 41089 To appear in: Gene Received date: 12 October 2015 Accepted date: 27 December 2015 Please cite this article as: Govindaraj, Lekha, Gupta, Tania, Esvaran, Vijaya Gowri, Awasthi, Aravind Kumar, Ponnuvel, Kangayam M., Genome – wide identification, characterization of sugar transporters genes in the silkworm Bombyx mori and role in Bombyx mori nucleopolyhedrovirus (BmNPV) infection, Gene (2015), doi: 10.1016/j.gene.2015.12.057 This is a PDF file of an unedited manuscript that has been accepted for publication.. As a service to our customers we are providing this early version of the manuscript.. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.

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A) Schematic representation of the daily distribution of metabolic processes resulting from the transcriptional signature of several differentially expressed genes throughout the 24-hour cycle. The different metabolic processes are indicated by gradiently colored arrows showing the time of the day corresponding to the higher expression levels of gene groups. The lengths of the arrows and darker colors indicate, respectively, intervals and peaks of expression. Local times are indicated at the bottom of the figure where an indicative representation of light intensity is also shown. The breakdown of energy-yielding nutrients (glycolysis, the Krebs cycle and the electron transport chain) and energy storage pathways (glycogen synthesis and fatty acid synthesis) are specifically activated in the early morning, while glycogen mobilization, gluconeogenesis and fatty acids catabolism are used as a stored energy source in the evening and throughout the night. B) Gene expression profiles of transcripts involved in energetic and metabolic processes are represented. The color of each gene corresponds to the metabolic process in which it is involved. Dashed lines indicate differentially expressed genes identified by a one-way ANOVA test, while solid lines represent differentially expressed genes characterized by a sinusoidal expression patterns detected by CircWaveBatch analysis. Microarray expression values are represented as log 2 mean ± standard deviation. Genes are represented with the following abbreviations: fructose 1,6-bisphosphatase ( FB ), glyceraldehyde-3-phosphate dehydrogenase ( GPD ), pyruvate kinase ( PK ), 6-phosphofructokinase ( 6P ), citrate synthase ( CS ), ATP synthase b ( ATP ), succinate dehydrogenase type C ( SD ), isocitrate dehydrogenase [NAD] subunit beta mitochondrial ( ID ), Acetyl-CoA acetyltransferase ( ACA ), short-chain specific acyl-CoA dehydrogenase ( ACD ), Acetyl-CoA carboxylase ( ACC ), ATP citrate lyase subunit beta ( ACL ), glycogen debranching enzyme-like ( GDE ), glycogen synthase ( GS ), and Glycogenin-1 ( G ).

Journal: PLoS ONE

Article Title: The Antarctic Krill Euphausia superba Shows Diurnal Cycles of Transcription under Natural Conditions

doi: 10.1371/journal.pone.0068652

Figure Lengend Snippet: A) Schematic representation of the daily distribution of metabolic processes resulting from the transcriptional signature of several differentially expressed genes throughout the 24-hour cycle. The different metabolic processes are indicated by gradiently colored arrows showing the time of the day corresponding to the higher expression levels of gene groups. The lengths of the arrows and darker colors indicate, respectively, intervals and peaks of expression. Local times are indicated at the bottom of the figure where an indicative representation of light intensity is also shown. The breakdown of energy-yielding nutrients (glycolysis, the Krebs cycle and the electron transport chain) and energy storage pathways (glycogen synthesis and fatty acid synthesis) are specifically activated in the early morning, while glycogen mobilization, gluconeogenesis and fatty acids catabolism are used as a stored energy source in the evening and throughout the night. B) Gene expression profiles of transcripts involved in energetic and metabolic processes are represented. The color of each gene corresponds to the metabolic process in which it is involved. Dashed lines indicate differentially expressed genes identified by a one-way ANOVA test, while solid lines represent differentially expressed genes characterized by a sinusoidal expression patterns detected by CircWaveBatch analysis. Microarray expression values are represented as log 2 mean ± standard deviation. Genes are represented with the following abbreviations: fructose 1,6-bisphosphatase ( FB ), glyceraldehyde-3-phosphate dehydrogenase ( GPD ), pyruvate kinase ( PK ), 6-phosphofructokinase ( 6P ), citrate synthase ( CS ), ATP synthase b ( ATP ), succinate dehydrogenase type C ( SD ), isocitrate dehydrogenase [NAD] subunit beta mitochondrial ( ID ), Acetyl-CoA acetyltransferase ( ACA ), short-chain specific acyl-CoA dehydrogenase ( ACD ), Acetyl-CoA carboxylase ( ACC ), ATP citrate lyase subunit beta ( ACL ), glycogen debranching enzyme-like ( GDE ), glycogen synthase ( GS ), and Glycogenin-1 ( G ).

Article Snippet: Probes were designed using the Agilent eArray Custom Microarray Design Service ( https://earray.chem.agilent.com/earray/index.jsp ), which applies proprietary prediction algorithms to design 60 mer oligo-probes.

Techniques: Expressing, Microarray, Standard Deviation