AMT Accesses Technology for Treatment of Duchenne Muscular Dystrophy
... will start its pre-clinical phase this year." exon skipping in DMD exon skipping is a technology to neutralize genetic ... cannot take place. However, when the faulty exon is eliminated (i.e. skipped), protein synthesis ...In vivo visualization of alternative splicing
... changes during the lifetime of the worm: Embryos and early larvae express exon 9, while adult worms express exon 10. By linking exons 9 and 10 with differently colored fluorescent ...First Catalog Cancer Biochip for Sequence Capture Now Available from febit
... febit will stay at the forefront of cancer research and include key research study results in the next generation of febit's cancer biochips. A 2Mb exon cancer biochip will be available this summer and a 30Mb biochip is planned already for release in 2010. Multiplex NGS studies based on ...Jivan Focuses on Solutions for Transcriptome Sequencing
... Arrays for targeted sequencing of genomes, gene families and therapeutic areas. By using Jivan's database of mRNA sequences, including exons and exon junctions, Jivan can ensure the capture of all mRNA sequences of each gene of interest, including wildtype transcripts and splice variants. For genes ...Jivan Awarded US Patent #7,340,349 for Splice Array Analysis
... The issued claims cover mathematical algorithms for determining the expression levels of splice isoforms of a gene in a sample using microarrays with exon junction probes. "The '349 Patent validates JIVAN's position as a leader in the growing market for DNA microarrays to detect alternative splicing," ...Heteroduplex Analysis Using the DCode System
... exons 7 and 10. The heterozygous mutations from exon 7 were 1154insTC, two base insertion ... deletion (-TTC). The mutations from exon 10 were a heterozygous ΔF508, three base ... to create end products of 289 bp for exon 7 and 369 bp ...Detection of Mutations in the CYP21 Gene Using the DCode System
... at the following nucleotide positions: exon 2: 2011 (A→C) and exon 5: 2851 (T→G). Nucleotide ... M12792; M23280. The mutant control sample for exon 6 contains the cluster-E6 mutation and ...Rapid detection of genomic duplications and deletions using the Agilent 2100 bioanalyzer
... each hybridization several DMD gene exon probes were chosen, both within and outside ... status was known4. For each sample at least 1 exon was chosen within the deleted/duplicated ... exon specific peaks were all normalized against ...Protein Truncation Tests Using the DCode System
... indicated a deletion of 174 bp, corresponding to the entire exon 26. Because this cDNA mutation would result in an in-frame ... a homozygous G to A substitution at the last nucleotide of exon 26 (nt 3576). This mutation is referred to as 3576 G > A ...Detection of Mutant K-ras in a Kindred With Hereditary Pancreatic Cancer by DGGE
... from tissue or from fluid obtained from patients at ERCP. K-ras exon 1 was amplified from genomic DNA using a thermal cycler and ... Prism (Perkin Elmer). Results exon 1, containing codons 12 and 13, of the K-ras gene was examined for ...Efficient Cellular Fractionation for RNA and Protein Isolation
... (35 cycles), both forms of the alternatively spliced fibronectin exon EIIIb mRNA were detected in total, cytoplasmic, and nuclear ... The mutually exclusive alternative splicing of fibronectin exon EIIIb was analyzed by RT-PCR (35 cycles) using total (T), ...Mutation detection for the K- rasand P16 genes
... shown to be mutated, sequencing can pinpoint the exact mutation. For P16 exon 3, the PCRs are electrophoresed on the Agilent 2100 bioanalyzer, ... sequence chromatograms for these samples. The analysis of the exon 3 region of the P16 gene was researched. At first, the discovery of ...The TripleMaster PCR System for three different amplifications
... -actin gene was amplified. The intron sequence between exon 1 and exon 2 of the human -actin gene has 85 % GC content and contains ...Efficient and Reliable PCR Setup Using Eppendorf MasterMix
... fragment length and template Lane 1: 160-bp fragment from exon 26 of the human gene of the apolipoprotein B, (genomic DNA) Lane 2: 360-bp fragment from exon 26 of the human gene of the apolipoprotein B, (genomic DNA) ...Gene-Specific Primers for NMDA Receptor Subunits
... NR1, Rat; flanking C1 exon C1 + , 214 C1 , 103 NR1, Rat: flanking N1 exon N1 + , 235 N1 ,172 ...SNPs Powerful Tools for Association Studies
... case, the nucleotide change that results in a RFLP is also the causative change (i.e., an A-to-T change in the number two nucleotide of the sixth exon in the - globin chain of the hemoglobin gene, Kan and Dozy, 1978). However, RFLPs only very rarely cause phenotypes and the number of RFLP markers ...Temporal Temperature Gradient Electrophoresis: A Powerful Technique to Screen Mutations
... Methods Mutant and wild-type genomic DNA were isolated from cell cultures. The samples were amplified for exon 8 of the p53 gene according to Borresen et al., using a 20-mer primer (5-ATCCTGAGTAGTGGTAATCT- 3) and a 60-mer primer ...Separation of HLA-DRB Alleles by Denaturing Gradient Gel Electrophoresis using the DCode System
... Here we describe a method for the separation of HLA-DRB alleles, following PCR amplification of the highly variable second exon of HLA-DRB alleles, using denaturing gradient gel electrophoresis (DGGE). When separation of HLA-DRB alleles is followed by direct ...Thermal Cycling Profile for Standard PCR
... Figure 1: Effect of excessive cycling on impure and pure templates A PCR product (245 bp amplicon from exon 6 of the dopamine 2 receptor gene) was reamplified in a series of reactions. In one set of experiments, the template was not ...The GeneZoo or the GeneJungle?
... new discoveries. The raw sequence of the human genome is now mostly complete, but it will be quite some time before all of the genes and their exon structures are known. Gene finding software programs are inaccurate at spotting exon-intron junctions. They can split groups of contiguous ...Fluorescence-Based Single-Tube Assays to Rapidly Detect Human Gene Mutations
... designed to rapidly detect/screen the most common mutation that causes cystic fibrosis (CF). This mutation, a three-base-pair deletion, within exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, accounts for approximately 70% of all mutant CF alleles. 3,4 The ...Brilliant Core Reagent Kits for QPCR and QRT-PCR
... quantitative PCR core reagent kit with another commercially available core reagent kit to amplify and detect a 294-bp region in exon 3 of the human b -actin gene using a TaqMan probe (Figure 1). Three concentrations (100, 1, and 0.01 ng) of human genomic DNA ...