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Bioedit Company tblastn program
Tblastn Program, supplied by Bioedit Company, 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/tblastn+programs/tblastn+program/pm39791875-123-5-35
Average 90 stars, based on 1 article reviews
tblastn program - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Sequencing:

Article Title: Coinducible Catabolism of 1-Naphthol via Synergistic Regulation of the Initial Hydroxylase Genes in Sphingobium sp. Strain B2
Article Snippet: .. To clone the genes involved in 1-naphthol catabolism in strain B2, sequences of previously reported enzymes related to downstream catabolism of 1-naphthol were subjected to local BLAST searches against the genome sequence of strain B2 (GenBank accession number {"type":"entrez-nucleotide","attrs":{"text":"VDBZ00000000","term_id":"1710613412","term_text":"VDBZ00000000"}} VDBZ00000000 ) using the tblastn program in BioEdit, because we supposed that enzymes for the downstream catabolism of 1-naphthol are conserved. ..

Article Title: Cultivation and mating of the truffle Tuber japonicum in plantations of ectomycorrhizal Quercus serrata seedlings.
Article Snippet: .. A local BLAST using the tblastn program was conducted utilizing the amino acid sequence of the MAT1-1-1 gene of T. borchii (PUU82705) as a query to identify a potential MAT1-1-1 gene with high affinity, using BioEdit Ver. ..

Article Title: Characterization and catalytic mechanism of a direct demethylsulfide hydrolase for catabolism of the methylthiol-s-triazine prometryn.
Article Snippet: • ProA from the strain JW-1 was successfully identified and characterized.. • ProA catalyzes the conversion of prometryne to 2-hydroxyprometryne and

other:

Article Title: Genome-Wide Analysis of the Rhododendron AP2/ERF Gene Family: Identification and Expression Profiles in Response to Cold, Salt and Drought Stress
Article Snippet: We created a local BLAST database with the Unigenes in the RNA-seq data and processed the tblastn search program with the RsAP2 protein sequence using BioEdit software (version 7.2.5).

Article Title: Transcriptomic characterisation of neuropeptides and their putative cognate G protein-coupled receptors during late embryo and stage-1 juvenile development of the Aotearoa-New Zealand crayfish, Paranephrops zealandicus.
Article Snippet: We de novo assembled a transcriptome for early life-stages of the Aotearoa-New Zealand crayfish, Paranephrops zealandicus, establishing the first genetic resource for this under-developed aquaculture species and for the Paranephrops genus.. Mining of this transcriptome for neuropeptides and their putative cognate G protein-coupled receptors (GPCRs) yielded a comprehensive catalogue of neuropeptides, but few putative neuropeptide GPCRs.. Of the neuropeptides commonly identified from decapod transcriptomes, only crustacean female sex hormone and insulin-like peptide were absent from our trinity de novo transcriptome assembly, and also RNA-sequence reads.

Article Title: Identification of Neuropeptides Using Long-Read RNA-Seq in the Swimming Crab Portunus trituberculatus , and Their Expression Profile Under Acute Ammonia Stress
Article Snippet: In addition, we carried out a local tblastn analysis with Bioedit 7.0.5.3 software, using the known crustacean neuropeptide precursors which were primarily from Nephrops norvegicus , Lysmata vittata , and S. paramamosain , as query sequences.

RNA sequencing:

Article Title: Selection of Reference Genes for qRT-PCR Analysis in Medicinal Plant Glycyrrhiza under Abiotic Stresses and Hormonal Treatments
Article Snippet: .. Protein sequences of these candidates were downloaded from the NCBI database; nucleotide sequences of these genes were obtained from G. uralensis genome ( http://ngs-data-archive.psc.riken.jp/Gur-genome/index.pl #) and G. inflata RNA-Seq database (SRA accession: PRJNA574093) using TBLASTN program in BioEdit software. .. Four new generation candidate genes ( ABCC2 , COPS3 , CS, and R3HDM2 ) were selected from the RNA-seq data and expressed consistently in different RNA-Seq samples. qRT-PCR primers were designed using PrimerQuest Tool, INTEGRATED DNA TECHNOLOGIES (IDT) ( https://sg.idtdna.com/Primerquest/Home/Index ).



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