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complementary dna microarray analysis hybridization  (Thermo Fisher)


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    Thermo Fisher complementary dna microarray analysis hybridization
    Complementary Dna Microarray Analysis Hybridization, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/complementary+dna+(cdna)+microarray+system/DNA/pm26411367-180-0-9
    Average 99 stars, based on 1 article reviews
    complementary dna microarray analysis hybridization - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Isolation:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Microarray:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Article Title: IL-4 blocks TH1-polarizing/inflammatory cytokine gene expression during monocyte-derived dendritic cell differentiation through histone hypoacetylation.
    Article Snippet: Background: Whereas recent research has characterized the mechanism by which dendritic cells (DCs) induce TH1/TH17 responses, the functional specialization enabling DCs to polarize TH2 responses remains undefined.. Because IL-4 is essential during TH2 responses not only by acting on CD4 1 T cells through the activation of GATA-3 but also by regulating IgE class-switching, epithelial cell permeability, and muscle contractility, we hypothesized that IL-4 could also have a role in the conditioning of DCs during TH2 responses.. Objective: We sought to analyze whether IL-4 exerts an immunomodulatory function on DCs during their differentiation, leading to their functional specialization for the induction of TH2 responses.

    Article Title: PKBalpha/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival.
    Article Snippet: For cell growth/viability experiments, cells were harvested daily and analyzed by trypan blue dye exclusion method with the Vicell CoulterCounter (Beckman). .. Microarray Analysis of DNA Damage-Induced Transcriptional Changes Total RNA was extracted from triplicate experiments using TRIzol (Invitrogen) according to the manufacturer’s instructions. cDNA was synthesized from 2 mg total RNA using the SuperScript cDNA system (Invitrogen) and used to generate biotin-labeled cRNA with the Enzo BioArray High Yield RNA transcript labeling kit (Enzo Diagnostics, USA). .. After fragmentation, 10 mg cRNA was hybridized with the mouse MOE430A 2.0 GeneChips (Affymetrix, Santa Clara, USA) following the protocol recommended by Affymetrix.

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 × 60 v2 microarray kit (Agilent Technologies), according to the manufacturers' protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 60 v2 microarray kit (Agilent Technologies), according to the manufacturers’ protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: Identification and characterization of proliferative retinopathy-related long noncoding RNAs.
    Article Snippet: Accepted Manuscript Identification and characterization of proliferative retinopathy-related long noncoding RNAs Rong-Mei Zhou, Xiao-Qun Wang, Jin Yao, Yi Shen, Sai-Nan Chen, Hong Yang, Qin Jiang, Biao Yan PII: S0006-291X(15)30352-1 DOI: 10.1016/j.bbrc.2015.07.120 Reference: YBBRC 34332 To appear in: Biochemical and Biophysical Research Communications Received Date: 14 July 2015 Accepted Date: 24 July 2015 Please cite this article as: R.-M. Zhou, X.-Q.. Wang, J. Yao, Y. Shen, S.-N. Chen, H. Yang, Q. Jiang, B. Yan, Identification and characterization of proliferative retinopathy-related long noncoding RNAs, Biochemical and Biophysical Research Communications (2015), doi: 10.1016/j.bbrc.2015.07.120.. This is a PDF file of an unedited manuscript that has been accepted for publication.

    Article Title: Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse
    Article Snippet: .. RNAs for microarray analysis were pooled for each group, purified using the RNeasy Micro Kit (Qiagen, Hilden, Germany) and reverse-transcribed to yield complementary DNA (cDNA) labeled with the fluorescent dye Cy3 or Cy5 using the SuperScript Indirect cDNA Labeling Core Kit (Invitrogen, CA, USA) and the SuperScript Indirect cDNA Labeling System Purification Kit (Invitrogen). .. Cy3- and Cy5-labeled samples were purified using the CyScribe GFX Purification Kit (GE Healthcare Bio-Sciences, Little Chalfont, UK).

    Hybridization:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Reverse Transcription:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 × 60 v2 microarray kit (Agilent Technologies), according to the manufacturers' protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 60 v2 microarray kit (Agilent Technologies), according to the manufacturers’ protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse
    Article Snippet: .. RNAs for microarray analysis were pooled for each group, purified using the RNeasy Micro Kit (Qiagen, Hilden, Germany) and reverse-transcribed to yield complementary DNA (cDNA) labeled with the fluorescent dye Cy3 or Cy5 using the SuperScript Indirect cDNA Labeling Core Kit (Invitrogen, CA, USA) and the SuperScript Indirect cDNA Labeling System Purification Kit (Invitrogen). .. Cy3- and Cy5-labeled samples were purified using the CyScribe GFX Purification Kit (GE Healthcare Bio-Sciences, Little Chalfont, UK).

    Polymerase Chain Reaction:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Gene Expression:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 × 60 v2 microarray kit (Agilent Technologies), according to the manufacturers' protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 60 v2 microarray kit (Agilent Technologies), according to the manufacturers’ protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Purification:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Article Title: Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse
    Article Snippet: .. RNAs for microarray analysis were pooled for each group, purified using the RNeasy Micro Kit (Qiagen, Hilden, Germany) and reverse-transcribed to yield complementary DNA (cDNA) labeled with the fluorescent dye Cy3 or Cy5 using the SuperScript Indirect cDNA Labeling Core Kit (Invitrogen, CA, USA) and the SuperScript Indirect cDNA Labeling System Purification Kit (Invitrogen). .. Cy3- and Cy5-labeled samples were purified using the CyScribe GFX Purification Kit (GE Healthcare Bio-Sciences, Little Chalfont, UK).

    Produced:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Labeling:

    Article Title: Glucocorticoids plus opioids up-regulate genes that influence neuronal function.
    Article Snippet: 1) This study investigated the functional genomics of glucocorticoid and opioid receptor stimulation in cellular adaptations using a cultured neuronal cell model.(2) Human SH-SY5Y neuroblastoma cells grown in hormone-depleted serum were treated for 2-days with the glucocorticoid receptor-II agonist dexamethasone (30 nM); the l-opioid receptor agonist [D-Ala2, N-Me-Phe4, Gly5-ol]-Enkephalin acetate (DAMGO; 1 nM); or dexamethasone (30 nM) plus DAMGO (1 nM).. RNA was extracted; purified, reverse transcribed, and labeled cDNA was hybridized to a 10,000-oliogonucleotide-array human gene chip.. Gene expression changes that were significantly different between treatment groups and were of interest due to biological function were verified by real-time reverse transcription polymerase chain reaction (RT-PCR).

    Article Title: IL-4 blocks TH1-polarizing/inflammatory cytokine gene expression during monocyte-derived dendritic cell differentiation through histone hypoacetylation.
    Article Snippet: Background: Whereas recent research has characterized the mechanism by which dendritic cells (DCs) induce TH1/TH17 responses, the functional specialization enabling DCs to polarize TH2 responses remains undefined.. Because IL-4 is essential during TH2 responses not only by acting on CD4 1 T cells through the activation of GATA-3 but also by regulating IgE class-switching, epithelial cell permeability, and muscle contractility, we hypothesized that IL-4 could also have a role in the conditioning of DCs during TH2 responses.. Objective: We sought to analyze whether IL-4 exerts an immunomodulatory function on DCs during their differentiation, leading to their functional specialization for the induction of TH2 responses.

    Article Title: PKBalpha/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival.
    Article Snippet: For cell growth/viability experiments, cells were harvested daily and analyzed by trypan blue dye exclusion method with the Vicell CoulterCounter (Beckman). .. Microarray Analysis of DNA Damage-Induced Transcriptional Changes Total RNA was extracted from triplicate experiments using TRIzol (Invitrogen) according to the manufacturer’s instructions. cDNA was synthesized from 2 mg total RNA using the SuperScript cDNA system (Invitrogen) and used to generate biotin-labeled cRNA with the Enzo BioArray High Yield RNA transcript labeling kit (Enzo Diagnostics, USA). .. After fragmentation, 10 mg cRNA was hybridized with the mouse MOE430A 2.0 GeneChips (Affymetrix, Santa Clara, USA) following the protocol recommended by Affymetrix.

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 × 60 v2 microarray kit (Agilent Technologies), according to the manufacturers' protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: A Host Susceptibility Gene, DR1, Facilitates Influenza A Virus Replication by Suppressing Host Innate Immunity and Enhancing Viral RNA Replication
    Article Snippet: Total RNA at 6 hpi was isolated by using a High Pure RNA isolation kit (Roche). .. Ten micrograms of RNA of each sample was reverse transcribed into cDNA and labeled with Alexa Fluor 555 by using the SuperScript Plus Indirect cDNA labeling system (Invitrogen), and the labeled cDNA was hybridized by using a SurePrint G3 human gene expression 8 60 v2 microarray kit (Agilent Technologies), according to the manufacturers’ protocols. .. Expression analysis and Gene Ontology (GO) analysis were performed by using GeneSpring 12 software (Agilent Technologies).

    Article Title: Identification and characterization of proliferative retinopathy-related long noncoding RNAs.
    Article Snippet: Accepted Manuscript Identification and characterization of proliferative retinopathy-related long noncoding RNAs Rong-Mei Zhou, Xiao-Qun Wang, Jin Yao, Yi Shen, Sai-Nan Chen, Hong Yang, Qin Jiang, Biao Yan PII: S0006-291X(15)30352-1 DOI: 10.1016/j.bbrc.2015.07.120 Reference: YBBRC 34332 To appear in: Biochemical and Biophysical Research Communications Received Date: 14 July 2015 Accepted Date: 24 July 2015 Please cite this article as: R.-M. Zhou, X.-Q.. Wang, J. Yao, Y. Shen, S.-N. Chen, H. Yang, Q. Jiang, B. Yan, Identification and characterization of proliferative retinopathy-related long noncoding RNAs, Biochemical and Biophysical Research Communications (2015), doi: 10.1016/j.bbrc.2015.07.120.. This is a PDF file of an unedited manuscript that has been accepted for publication.

    Article Title: Maternal exposure to nanoparticulate titanium dioxide during the prenatal period alters gene expression related to brain development in the mouse
    Article Snippet: .. RNAs for microarray analysis were pooled for each group, purified using the RNeasy Micro Kit (Qiagen, Hilden, Germany) and reverse-transcribed to yield complementary DNA (cDNA) labeled with the fluorescent dye Cy3 or Cy5 using the SuperScript Indirect cDNA Labeling Core Kit (Invitrogen, CA, USA) and the SuperScript Indirect cDNA Labeling System Purification Kit (Invitrogen). .. Cy3- and Cy5-labeled samples were purified using the CyScribe GFX Purification Kit (GE Healthcare Bio-Sciences, Little Chalfont, UK).

    Amplification:

    Article Title: IL-4 blocks TH1-polarizing/inflammatory cytokine gene expression during monocyte-derived dendritic cell differentiation through histone hypoacetylation.
    Article Snippet: Background: Whereas recent research has characterized the mechanism by which dendritic cells (DCs) induce TH1/TH17 responses, the functional specialization enabling DCs to polarize TH2 responses remains undefined.. Because IL-4 is essential during TH2 responses not only by acting on CD4 1 T cells through the activation of GATA-3 but also by regulating IgE class-switching, epithelial cell permeability, and muscle contractility, we hypothesized that IL-4 could also have a role in the conditioning of DCs during TH2 responses.. Objective: We sought to analyze whether IL-4 exerts an immunomodulatory function on DCs during their differentiation, leading to their functional specialization for the induction of TH2 responses.

    Synthesized:

    Article Title: PKBalpha/Akt1 acts downstream of DNA-PK in the DNA double-strand break response and promotes survival.
    Article Snippet: For cell growth/viability experiments, cells were harvested daily and analyzed by trypan blue dye exclusion method with the Vicell CoulterCounter (Beckman). .. Microarray Analysis of DNA Damage-Induced Transcriptional Changes Total RNA was extracted from triplicate experiments using TRIzol (Invitrogen) according to the manufacturer’s instructions. cDNA was synthesized from 2 mg total RNA using the SuperScript cDNA system (Invitrogen) and used to generate biotin-labeled cRNA with the Enzo BioArray High Yield RNA transcript labeling kit (Enzo Diagnostics, USA). .. After fragmentation, 10 mg cRNA was hybridized with the mouse MOE430A 2.0 GeneChips (Affymetrix, Santa Clara, USA) following the protocol recommended by Affymetrix.



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