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genotype  (Rupali Instruments)

 
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    Rupali Instruments genotype
    Genotype, supplied by Rupali Instruments, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/genotypes/1+genotype+rupali/pmc13253189-22-41-4
    Average 86 stars, based on 1 article reviews
    genotype - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Infection:

    Article Title: Rapid and High Throughput Hydroponics Phenotyping Method for Evaluating Chickpea Resistance to Phytophthora Root Rot
    Article Snippet: .. Chickpea genotypes (Rupali, Yorker, and 04067-81-2-1-1) growing under the combination of hypoxia and P. medicaginis infection showed more foliar symptoms and root disease than aerated infected plants [ ]. ..

    other:

    Article Title: Morphological and Genetic Variability in French Bean
    Article Snippet: Wide variation in plant height was observed among French bean genotypes ranging from 34.36 cm in 'Rupali' to 46.97 cm in 'NFL-35' with a mean of 40.11 cm.

    Article Title: Rapid and High Throughput Hydroponics Phenotyping Method for Evaluating Chickpea Resistance to Phytophthora Root Rot
    Article Snippet: Roots of three genotypes, 04067-81-2-1-1, Yorker, and Rupali, representing three distinct groups of resistance (MR-MS, S, and VS, respectively), were harvested at the end of E1, dried at 40 °C for 72 h, weighed, placed in 200 g of sand, and sent to the South Australian Research and Development Institute (Adelaide, Australia) to quantify P. medicaginis DNA concentration via qPCR as described by Bithell et al. [ ].

    Article Title: Seed priming with NaCl helps to improve tissue tolerance, potassium retention ability of plants, and protects the photosynthetic ability in two different legumes, chickpea and lentil, under salt stress.
    Article Snippet: Main conclusion Seed priming with NaCl mimicked the conditions of natural priming to improve the tissue tolerance nature of sensitive legumes, which helps to maintain survivability and yield in mildly saline areas.. Abstract Seed priming with NaCl is a seed invigoration technique that helps to improve plant growth by altering Na+ and K+ content under salt stress.. Legumes are overall sensitive to salt and salinity hampers their growth and yield.

    Article Title: Superior Salt Tolerance in Wild Soybean (G. soja) is Associated With Better Ion ‘Exclusion’ Ability From Leaves and Mesophyll Cells Than Cultivated Soybean Genotypes (G. max)
    Article Snippet: Soybean (Glycine max) is a salt-sensitive crop.. However, wild soybean (Glycine soja) is a potential source of germplasm to improve salt tolerance in G. max.. This study evaluated the response of cultivated soybean (G. max cv.

    Article Title: Growth performance, egg quality and selection intensity of 6th generation of BLRI improved native duck genotypes
    Article Snippet: Bangladesh Livestock Research Institute (BLRI) has been selecting two native duck genotypes, BLRI duck 1 (Rupali) and (Nageswari) for generations.

    Control:

    Article Title: Molecular Approaches to Improve Legume Salt Stress Tolerance
    Article Snippet: The global challenge of crop loss due to salt stress became increasingly significant, especially in the context of meeting the rising demands of a growing world population.. This review focuses on the impact of salt stress on leguminous plants throughout their entire growth stages.. Additionally, it provides a comprehensive overview of the molecular strategies employed to enhance the performance of legumes in saline environments.

    Concentration Assay:

    Article Title: Molecular Approaches to Improve Legume Salt Stress Tolerance
    Article Snippet: The global challenge of crop loss due to salt stress became increasingly significant, especially in the context of meeting the rising demands of a growing world population.. This review focuses on the impact of salt stress on leguminous plants throughout their entire growth stages.. Additionally, it provides a comprehensive overview of the molecular strategies employed to enhance the performance of legumes in saline environments.



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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