dhplc (wave dna fragment analysis system, dnasep column (Transgenomic)
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Transgenomic
dhplc (wave dna fragment analysis system, dnasep column
Dhplc (Wave Dna Fragment Analysis System, Dnasep Column, supplied by Transgenomic, 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/dhplc+analysis/dhplc++wave+dna+fragment+analysis+system++dnasep+column/pmc02435537-75-13-20
Average 90 stars, based on 1 article reviews
Dhplc (Wave Dna Fragment Analysis System, Dnasep Column, supplied by Transgenomic, 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/dhplc+analysis/dhplc++wave+dna+fragment+analysis+system++dnasep+column/pmc02435537-75-13-20
Average 90 stars, based on 1 article reviews
dhplc (wave dna fragment analysis system, dnasep column - by Bioz Stars,
2026-10
90/100 stars
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Polymerase Chain Reaction:Article Title: Variation in NCB5OR Article Snippet: .. The mixed PCR products were denatured at 95°C for 5 min, renatured at room temperature for 30 min, and analyzed by dHPLC using the Article Title: NOTCH mutations leading to increased receptor signaling Article Snippet: .. DNAs were resuspended in TE buffer, spectrophotometrically quantified and stored at −20° C. Mutation Detection Mutation detection in exons 26, 27, and 34 of NOTCH-1 was performed via PCR-based denaturing HPLC using a Article Title: Paramyotonia congenita: From clinical diagnosis toin silicoprotein modeling analysis Article Snippet: Background: Paramyotonia congenita (PMC) is an autosomal dominant disorder characterized by coldor exerciseinduced myotonia.. PMC is caused by a mutation in SCN4A which encodes the a-subunit of the skeletal muscle sodium channel.. Methods: The patient was an 11-year-old Japanese girl who was diagnosed as having PMC. Mutagenesis:Article Title: NOTCH mutations leading to increased receptor signaling Article Snippet: .. DNAs were resuspended in TE buffer, spectrophotometrically quantified and stored at −20° C. Mutation Detection Mutation detection in exons 26, 27, and 34 of NOTCH-1 was performed via PCR-based denaturing HPLC using a High Performance Liquid Chromatography:Article Title: NOTCH mutations leading to increased receptor signaling Article Snippet: .. DNAs were resuspended in TE buffer, spectrophotometrically quantified and stored at −20° C. Mutation Detection Mutation detection in exons 26, 27, and 34 of NOTCH-1 was performed via PCR-based denaturing HPLC using a Article Title: A role of ADAR2 and RNA editing of glutamate receptors in mood disorders and schizophrenia Article Snippet: .. The reaction mixture was separated and quantified by denaturing HPLC using a Article Title: Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis. Article Snippet: This patient is the 12-year-old first child of healthy unrelated parents.. The parents do, however, come from the same small mountain village in northern Italy (2200 inhabitants) and have the same surname.. The patient has a healthy 9year-old brother. Article Title: Paramyotonia congenita: From clinical diagnosis toin silicoprotein modeling analysis Article Snippet: Background: Paramyotonia congenita (PMC) is an autosomal dominant disorder characterized by coldor exerciseinduced myotonia.. PMC is caused by a mutation in SCN4A which encodes the a-subunit of the skeletal muscle sodium channel.. Methods: The patient was an 11-year-old Japanese girl who was diagnosed as having PMC. Sequencing:Article Title: Novel mutations in of the ABCR gene in Italian patients with Stargardt disease. Article Snippet: .. Mutational analysis Sequence variations were detected by denaturing highperformance liquid chromatography (DHPLC) using the Liquid Chromatography:Article Title: Novel mutations in of the ABCR gene in Italian patients with Stargardt disease. Article Snippet: .. Mutational analysis Sequence variations were detected by denaturing highperformance liquid chromatography (DHPLC) using the Software:Article Title: Novel mutations in of the ABCR gene in Italian patients with Stargardt disease. Article Snippet: .. Mutational analysis Sequence variations were detected by denaturing highperformance liquid chromatography (DHPLC) using the other:Article Title: Could a defective epithelial sodium channel lead to bronchiectasis Article Snippet: Mutation analysis of the patients with idiopathic bronchiectasis was performed by using Article Title: Trends in the Prevalence of Tuberous Sclerosis Complex Manifestations: An Epidemiological Study of 166 Japanese Patients Article Snippet: The PCR products were applied to a denaturing high performance liquid chromatography (DHPLC) machine, a WAVE® Nucleic Acid Fragment Analysis System equipped with a |