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house genotyping  (Transnetyx)


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    Structured Review

    Transnetyx house genotyping
    House Genotyping, supplied by Transnetyx, used in various techniques. Bioz Stars score: 99/100, based on 2198 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genotypes/Automated+Genotyping/pm42853877-315-10-5
    Average 99 stars, based on 2198 article reviews
    house genotyping - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    DNA Extraction:

    Article Title: Sex-Specific Proteomics Changes Induced by Genetic Deletion of the Fibroblast Growth Factor 14 (FGF14) Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    Article Title: Sex-Specific Proteomic Changes Induced by Genetic Deletion of Fibroblast Growth Factor 14 (FGF14), a Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    Polymerase Chain Reaction:

    Article Title: Sex-Specific Proteomics Changes Induced by Genetic Deletion of the Fibroblast Growth Factor 14 (FGF14) Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    Article Title: Sex-Specific Proteomic Changes Induced by Genetic Deletion of Fibroblast Growth Factor 14 (FGF14), a Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    Amplification:

    Article Title: Sex-Specific Proteomics Changes Induced by Genetic Deletion of the Fibroblast Growth Factor 14 (FGF14) Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    Article Title: Sex-Specific Proteomic Changes Induced by Genetic Deletion of Fibroblast Growth Factor 14 (FGF14), a Regulator of Neuronal Ion Channels
    Article Snippet: .. All of the genotypes described were confirmed by genotyping of the progeny using DNA extraction and PCR amplification following established protocols or conducted at Transnetyx Inc. (Cordova, TN, USA). ..

    other:

    Article Title: Interactome quantitation reveals non-energetic mitochondrial roles in cell type specialization in murine kidney.
    Article Snippet: Mice were housed at 20°C under diurnal conditions with ad libitum food and water in an AAALAC-accredited facility with supervision by the Institutional Animal Care and Use Committee at the University of Washington.

    Article Title: DHODH is an independent prognostic marker and potent therapeutic target in neuroblastoma.
    Article Snippet: Genotypes were determined from ear tissue biopsies using qPCR with specific probes designed for wild-type and the MYCN transgene (Transnetyx).

    Article Title: PPARgamma agonists rescue increased phosphorylation of FGF14 at S226 in the Tg2576 mouse model of Alzheimer's disease
    Article Snippet: The FGF14 S226A -GFP construct was generated using QuikChange Lightning kits protocol (Agilent Technologies Santa Clara, CA) using the following primers FW: 5′–GGTGACGCCAGCTAAAAGCACAAGT RV: 5′–CCACTGCGGTCGATTTTCGTGTTCA, and confirmed by sequencing at the Molecular Genomics Core Facility at the University of Texas Medical Branch, Galveston, TX.

    Real-time Polymerase Chain Reaction:

    Article Title: DHODH is an independent prognostic marker and potent therapeutic target in neuroblastoma
    Article Snippet: .. Genotypes were determined from ear tissue biopsies using qPCR with specific probes designed for wild-type and the MYCN transgene (Transnetyx, Cordova, TN, USA). ..



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    Image Search Results


    Workflow for identifying 38 candidate RNA-binding protein (RBP) genes potentially implicated in male infertility. This flowchart illustrates the stepwise strategy used to prioritize 38 candidate RBP genes for further investigation in male reproductive biology. The process began with mining the ‘male mouse germ cell RBPome’ database, comprising 408 RBPs enriched (n=168) and specific (n=240) to mouse testes. Human orthologs were identified through homology mapping and cross-referenced with expression data from the Genotype-Tissue Expression and Human Protein Atlas databases. A total of 339 RBPs were found to be expressed in human testicular tissue. Applying a selection criterion of testis-specific enrichment (≥5-fold higher mRNA expression in testis compared to other tissues), 163 testis-enriched human-mouse homologous RBP genes were retained. A comprehensive literature search (PubMed) was conducted to evaluate the functional relevance of these genes in male fertility. Of the 163 RBPs, 125 had previously been associated with reproductive phenotypes in mouse models. The remaining 38 genes (comprising 3 classical, 3 non-classical, and 32 novel RBPs) lacked knockout mouse models, representing a prioritized subset for future functional validation. GTEx, Genotype-Tissue Expression; HPA, Human Protein Atlas; KO, knockout; mMGC, male mouse germ cell.

    Journal: Human Reproduction Update

    Article Title: The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility

    doi: 10.1093/humupd/dmaf023

    Figure Lengend Snippet: Workflow for identifying 38 candidate RNA-binding protein (RBP) genes potentially implicated in male infertility. This flowchart illustrates the stepwise strategy used to prioritize 38 candidate RBP genes for further investigation in male reproductive biology. The process began with mining the ‘male mouse germ cell RBPome’ database, comprising 408 RBPs enriched (n=168) and specific (n=240) to mouse testes. Human orthologs were identified through homology mapping and cross-referenced with expression data from the Genotype-Tissue Expression and Human Protein Atlas databases. A total of 339 RBPs were found to be expressed in human testicular tissue. Applying a selection criterion of testis-specific enrichment (≥5-fold higher mRNA expression in testis compared to other tissues), 163 testis-enriched human-mouse homologous RBP genes were retained. A comprehensive literature search (PubMed) was conducted to evaluate the functional relevance of these genes in male fertility. Of the 163 RBPs, 125 had previously been associated with reproductive phenotypes in mouse models. The remaining 38 genes (comprising 3 classical, 3 non-classical, and 32 novel RBPs) lacked knockout mouse models, representing a prioritized subset for future functional validation. GTEx, Genotype-Tissue Expression; HPA, Human Protein Atlas; KO, knockout; mMGC, male mouse germ cell.

    Article Snippet: To identify candidate RBPs lacking knockout mouse models, we mined the RBP atlas and integrated transcriptomic and proteomic evidence from the Genotype-Tissue Expression (GTEx), Human Protein Atlas (HPA), and UniProt databases.

    Techniques: RNA Binding Assay, Expressing, Selection, Functional Assay, Knock-Out, Biomarker Discovery

    Integrated analysis of 163 testis-enriched RNA-binding proteins (RBPs): gene expression, functional enrichment, and protein-protein interaction (PPI). (A) Heatmap of RBP Gene Expression across Human Tissues (GTEx). Normalized expression levels of 163 testis-enriched RBP genes are shown across multiple human tissues using data from the GTEx database. Genes are arranged on the y -axis and tissues on the x -axis. Color intensity reflects expression levels (low: light yellow; high: dark blue). Genes with testis-specific enrichment (>5-fold higher expression in testes relative to other tissues) are highlighted by RBP classification: classical (blue, n=17), non-classical (green, n=26), and novel (red, n=120). This heatmap illustrates the tissue-specific expression landscape of RBPs, with a particular emphasis on testis-predominant expression. (B) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathway Enrichment Analyses. GO terms and KEGG pathways enriched among the 163 testis-enriched RBPs are depicted. The GO analysis includes biological process (BP), cellular component (CC), and molecular function (MF) categories, highlighting roles in spermatogenesis, RNA processing, and subcellular localization. KEGG analysis identifies key signaling and metabolic pathways relevant to testicular function and male fertility. (C) PPI network. A PPI network of testis-enriched RBPs was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins database. Nodes represent individual RBPs, and edges indicate predicted or known interactions, weighted by confidence scores. This network provides insight into the potential cooperative functions and regulatory hubs of RBPs involved in spermatogenesis and testicular physiology.

    Journal: Human Reproduction Update

    Article Title: The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility

    doi: 10.1093/humupd/dmaf023

    Figure Lengend Snippet: Integrated analysis of 163 testis-enriched RNA-binding proteins (RBPs): gene expression, functional enrichment, and protein-protein interaction (PPI). (A) Heatmap of RBP Gene Expression across Human Tissues (GTEx). Normalized expression levels of 163 testis-enriched RBP genes are shown across multiple human tissues using data from the GTEx database. Genes are arranged on the y -axis and tissues on the x -axis. Color intensity reflects expression levels (low: light yellow; high: dark blue). Genes with testis-specific enrichment (>5-fold higher expression in testes relative to other tissues) are highlighted by RBP classification: classical (blue, n=17), non-classical (green, n=26), and novel (red, n=120). This heatmap illustrates the tissue-specific expression landscape of RBPs, with a particular emphasis on testis-predominant expression. (B) Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) Pathway Enrichment Analyses. GO terms and KEGG pathways enriched among the 163 testis-enriched RBPs are depicted. The GO analysis includes biological process (BP), cellular component (CC), and molecular function (MF) categories, highlighting roles in spermatogenesis, RNA processing, and subcellular localization. KEGG analysis identifies key signaling and metabolic pathways relevant to testicular function and male fertility. (C) PPI network. A PPI network of testis-enriched RBPs was constructed using the Search Tool for the Retrieval of Interacting Genes/Proteins database. Nodes represent individual RBPs, and edges indicate predicted or known interactions, weighted by confidence scores. This network provides insight into the potential cooperative functions and regulatory hubs of RBPs involved in spermatogenesis and testicular physiology.

    Article Snippet: To identify candidate RBPs lacking knockout mouse models, we mined the RBP atlas and integrated transcriptomic and proteomic evidence from the Genotype-Tissue Expression (GTEx), Human Protein Atlas (HPA), and UniProt databases.

    Techniques: RNA Binding Assay, Gene Expression, Functional Assay, Expressing, Construct