dnastar lasergene editseq software (DNASTAR)
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DNASTAR
dnastar lasergene editseq software
Dnastar Lasergene Editseq Software, supplied by DNASTAR, used in various techniques. Bioz Stars score: 99/100, based on 10689 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dnastar+lasergene+editseq/Lasergene/pmc12887770-65-6-12
Average 99 stars, based on 10689 article reviews
Dnastar Lasergene Editseq Software, supplied by DNASTAR, used in various techniques. Bioz Stars score: 99/100, based on 10689 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dnastar+lasergene+editseq/Lasergene/pmc12887770-65-6-12
Average 99 stars, based on 10689 article reviews
dnastar lasergene editseq software - by Bioz Stars,
2026-09
99/100 stars
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Sequencing:Article Title: Characterization and identification of novel polymorphisms in the OR51H1 gene associated with resistance/tolerance to natural Theileria infection in Vechur (Bos indicus) and crossbred (B. taurus × B. indicus) cattle in a Theileria-endemic region. Article Snippet: Theileriosis is a haemo protozoan disease affecting livestock, causing high mortality and production loss.. Although therapeutic and vector control measures are available, selecting Theileria-resistant/tolerant animals is considered an alternate control measure for which the identification of genetic markers is essential.. The present study screened dwarf Vechur (Bos indicus) and crossbred (B. taurus × B. indicus) cattle for natural infection to Theileria using peripheral blood smear and clinical and haematology evaluation. Article Title: Involvement of glucose transporter 4 in ovarian development and reproductive maturation of Harmonia axyridis (Coleoptera: Coccinellidae). Article Snippet: .. Amino acid sequences were predicted 118 using Article Title: Protein polymer nanoparticles engineered as chaperones protect against apoptosis in human retinal pigment epithelial cells Article Snippet: .. Peptide label Amino Acid Sequence * Expected M.W. (kDa) ** Observed M.W. (kDa) SI G(VPGSG) 48 (VPGIG) 48 Y 39.65 39.54 crySI GDRFSVNLDVKHFSPEELKVKG(VPGSG) 48 (VPGIG) 48 Y 42.07 42.06 S96 G(VPGSG) 96 Y 38.39 38.22 cryS96 GDRFSVNLDVKHFSPEELKVKG(VPGSG) 96 Y 40.82 40.72 Open in a separate window * Expected M.W. (m/z) was calculated by other:Article Title: The Potential Role of Synanthropic Rodents and Flies in the Transmission of Enterocytozoon bieneusi on a Dairy Cattle farm in China. Article Snippet: Enterocytozoon bieneusi causes microsporidiosis, a condition with complex epidemiology involving both direct and indirect transmission routes.. To assess the potential role of synanthropic rodents and flies in the transmission of this pathogen, a total of 277 cattle fecal samples, 199 synanthropic rodents, and 50 batches of 20 flies were collected from a cattle farm.. These samples were screened for the presence of E. bieneusi by PCR and sequencing of the internal transcribed spacer (ITS) region of the rRNA gene. Binding Assay:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Eye Drops:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Sublimation:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Residue:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Selection:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Cloning:Article Title: Lacritin-mediated regeneration of the corneal epithelia by protein polymer nanoparticles Article Snippet: .. This cell targeting specicity is triggered by a unique ‘off-on’ switch controlled by heparanase deglycanation of the cell surface protein, syndecan1, which exposes a lacritin binding site as a prerequisite for its downstream mitogenic signaling.16,17 Although topical application of ophthalmic products has remained the most popular and well-tolerated administration route for patient compliance, the bioavailability of eye drops is severely hindered by blinking, baseline and reex lacrimation, and nasolacrimal drainage.18 One solution to enhance the therapeutic index of topical treatments is through the application of polymeric nanoparticles as drug carriers.19–21 Polymeric nanoparticles displaying therapeutic ligands at the corona can interact with complex biomolecular architectures through multiple simultaneous interactions (multivalency) and exhibit the well-dened sizes required for efficient tissue penetration.22 One suchmaterial capable of being employed as the scaffold are thermo-responsive elastin-like polypeptides (ELPs).23 ELPs are composed of the repetitive pentapeptide motif (Val-Pro-Gly-XaaGly)n and exhibit unique reversible inverse phase transition temperatures, Tt, below which they solubilize and above which they phase separate.24 Tt can be modulated through guest residue (Xaa) selection and changes in the number of pentameric repeats, n.25,26 We have previously reported the successful bioengineering of diblock ELP nanoparticles to suppress tumor growth with rapamycin binding at both the corona as well as in the core;27 uptake of ELP nanoparticles displaying adenovirus knob domain into hepatocytes and acinar cells has also been described.28 Moreover, Callahan and coworkers have demonstrated enhanced intratumoral spatial a Aer the start codon, a glycine spacer was added during cloning which is Software:Article Title: Spiralin diversity within Iranian strains of Spiroplasma citri. Article Snippet: The first-cultured and most-studied spiroplasma is Spiroplasma citri, the causal agent of citrus stubborn disease, one of the three plant-pathogenic, sieve-tuberestricted, and leafhopper vector-transmitted mollicutes.. In Iranian Fars province, S. citri cultures were obtained from stubborn affected citrus trees, sesame and safflower plants, and from the leafhopper vector Circulifer haematoceps.. Spiralin gene sequences from different S. citri isolates were amplified by PCR, cloned, and sequenced. Molecular Weight:Article Title: Protein polymer nanoparticles engineered as chaperones protect against apoptosis in human retinal pigment epithelial cells Article Snippet: .. Peptide label Amino Acid Sequence * Expected M.W. (kDa) ** Observed M.W. (kDa) SI G(VPGSG) 48 (VPGIG) 48 Y 39.65 39.54 crySI GDRFSVNLDVKHFSPEELKVKG(VPGSG) 48 (VPGIG) 48 Y 42.07 42.06 S96 G(VPGSG) 96 Y 38.39 38.22 cryS96 GDRFSVNLDVKHFSPEELKVKG(VPGSG) 96 Y 40.82 40.72 Open in a separate window * Expected M.W. (m/z) was calculated by |