luxscantm 10k-b microarray scanner (CapitalBio Corporation)
90
Structured Review
CapitalBio Corporation
luxscantm 10k-b microarray scanner
Luxscantm 10k B Microarray Scanner, supplied by CapitalBio Corporation, 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/luxscantm+10k-b+microarray+scanner/luxscan+10+k+microarray+scanner/pmc09884444-128-22-28
Average 90 stars, based on 1 article reviews
Luxscantm 10k B Microarray Scanner, supplied by CapitalBio Corporation, 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/luxscantm+10k-b+microarray+scanner/luxscan+10+k+microarray+scanner/pmc09884444-128-22-28
Average 90 stars, based on 1 article reviews
luxscantm 10k-b microarray scanner - by Bioz Stars,
2026-09
90/100 stars
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Extraction:Article Title: Screening and Drug Resistance Analysis of Non-Tuberculous Mycobacteria in Patients with Suspected Pulmonary Tuberculosis on the Hainan Island, China Article Snippet: SLideWasher TM 8 chip washing and drying instrument, Extractor TM 36 nucleic acid rapid extraction instrument, Article Title: Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children. Article Snippet: Objective: To investigate the mutations of SLC26A4 gene and the relevant phenotype in Chinese sporadic nonsyndromic hearing-impaired children.. Methods: 195 Chinese sporadic nonsyndromic hearing-impaired children were subjected to microarraybased mutation detection for 9 hot spot mutations in four of the most common deafness-related genes (GJB2, SLC26A4, GJB3, and 12s rRNA).. Subsequently, twenty-one patients with one SLC26A4 mutation detected by microarray were subjected to sequencing analysis of the whole SLC26A4 coding region and the splice sites in order to identify the second mutant allele. Article Title: Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families. Article Snippet: Objective: Genetic counseling and prenatal diagnosis are very necessary and accurate to detect hereditary hearing loss, especially in high-risk families.. Prenatal diagnosis is testing for diseases or conditions in fetuses before born, which gives parents the chance to prepare psychologically, financially and medically for the probable health and educational needs of the affected neonates.. Methods: 54 unrelated families with children affected with non-syndromic sensorineural hearing loss were enrolled in the study and received genetic analysis with microarray and DNA sequencing technologies. Hybridization:Article Title: Screening and Drug Resistance Analysis of Non-Tuberculous Mycobacteria in Patients with Suspected Pulmonary Tuberculosis on the Hainan Island, China Article Snippet: SLideWasher TM 8 chip washing and drying instrument, Extractor TM 36 nucleic acid rapid extraction instrument, Article Title: Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children. Article Snippet: Objective: To investigate the mutations of SLC26A4 gene and the relevant phenotype in Chinese sporadic nonsyndromic hearing-impaired children.. Methods: 195 Chinese sporadic nonsyndromic hearing-impaired children were subjected to microarraybased mutation detection for 9 hot spot mutations in four of the most common deafness-related genes (GJB2, SLC26A4, GJB3, and 12s rRNA).. Subsequently, twenty-one patients with one SLC26A4 mutation detected by microarray were subjected to sequencing analysis of the whole SLC26A4 coding region and the splice sites in order to identify the second mutant allele. Article Title: Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families. Article Snippet: Objective: Genetic counseling and prenatal diagnosis are very necessary and accurate to detect hereditary hearing loss, especially in high-risk families.. Prenatal diagnosis is testing for diseases or conditions in fetuses before born, which gives parents the chance to prepare psychologically, financially and medically for the probable health and educational needs of the affected neonates.. Methods: 54 unrelated families with children affected with non-syndromic sensorineural hearing loss were enrolled in the study and received genetic analysis with microarray and DNA sequencing technologies. Microarray:Article Title: Screening and Drug Resistance Analysis of Non-Tuberculous Mycobacteria in Patients with Suspected Pulmonary Tuberculosis on the Hainan Island, China Article Snippet: SLideWasher TM 8 chip washing and drying instrument, Extractor TM 36 nucleic acid rapid extraction instrument, Article Title: Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children. Article Snippet: Objective: To investigate the mutations of SLC26A4 gene and the relevant phenotype in Chinese sporadic nonsyndromic hearing-impaired children.. Methods: 195 Chinese sporadic nonsyndromic hearing-impaired children were subjected to microarraybased mutation detection for 9 hot spot mutations in four of the most common deafness-related genes (GJB2, SLC26A4, GJB3, and 12s rRNA).. Subsequently, twenty-one patients with one SLC26A4 mutation detected by microarray were subjected to sequencing analysis of the whole SLC26A4 coding region and the splice sites in order to identify the second mutant allele. Article Title: Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families. Article Snippet: Objective: Genetic counseling and prenatal diagnosis are very necessary and accurate to detect hereditary hearing loss, especially in high-risk families.. Prenatal diagnosis is testing for diseases or conditions in fetuses before born, which gives parents the chance to prepare psychologically, financially and medically for the probable health and educational needs of the affected neonates.. Methods: 54 unrelated families with children affected with non-syndromic sensorineural hearing loss were enrolled in the study and received genetic analysis with microarray and DNA sequencing technologies. |