نتایج جستجو برای: splicing by overlap extension pcr

تعداد نتایج: 7193854  

2017
Giulia Cardamone Elvezia Maria Paraboschi Valeria Rimoldi Stefano Duga Giulia Soldà Rosanna Asselta

Abnormalities in alternative splicing (AS) are emerging as recurrent features in autoimmune diseases (AIDs). In particular, a growing body of evidence suggests the existence of a pathogenic association between a generalized defect in splicing regulatory genes and multiple sclerosis (MS). Moreover, several studies have documented an unbalance in alternatively-spliced isoforms in MS patients poss...

Journal: :Journal of Experimental Botany 2009
Andrés P. Gagete Marta Riera Luis Franco M. Isabel Rodrigo

At least seven isoforms (PsABI3-1 to PsABI3-7) of a putative, pea ABI3-like factor, originated by alternative splicing, have been identified after cDNA cloning. A similar variability had previously only been described for monocot genes. The full-length isoform, PsABI3-1, contains the typical N-terminal acidic domains and C-terminal basic subdomains, B1 to B3. Reverse transcriptase-PCR analysis ...

2011
Katherine Sorber Michelle T. Dimon Joseph L. DeRisi

Over 50% of genes in Plasmodium falciparum, the deadliest human malaria parasite, contain predicted introns, yet experimental characterization of splicing in this organism remains incomplete. We present here a transcriptome-wide characterization of intraerythrocytic splicing events, as captured by RNA-Seq data from four timepoints of a single highly synchronous culture. Gene model-independent a...

Journal: :Microbes and environments 2009
Mei-Fang Chien Saeko Tosa Chieh-Chen Huang Ginro Endo

The splicing of a bacterial group II subclass B intron B.me.I1 from Bacillus megaterium chromosomes was investigated. RT-PCR and nucleic acid hybridization methods were used to understand the role of the intron-encoded protein (IEP) in the splicing of B.me.I1. An in vivo assay showed that the splicing occurred in the absence of IEP. An in vitro assay showed that B.me.I1 was spliced under condit...

2015
Lee M. Yeoh Christopher D. Goodman Nathan E. Hall Giel G. van Dooren Geoffrey I. McFadden Stuart A. Ralph

Single genes are often subject to alternative splicing, which generates alternative mature mRNAs. This phenomenon is widespread in animals, and observed in over 90% of human genes. Recent data suggest it may also be common in Apicomplexa. These parasites have small genomes, and economy of DNA is evolutionarily favoured in this phylum. We investigated the mechanism of alternative splicing in Tox...

Journal: :Journal of cell science 2006
Kimihiko Sugaya Etsuko Hongo Yoshie Ishihara Hideo Tsuji

Temperature-sensitive CHO-K1 mutant cell line tsTM18 exhibits chromosomal instability and cell-cycle arrest at S and G2 phases with decreased DNA synthesis at the nonpermissive temperature, 39 degrees C. We previously identified an amino acid substitution in Smu1 that underlies the temperature-sensitive phenotypes of tsTM18 cells. In the present study, we confirmed that Smu1 is associated with ...

Journal: :Clinical chemistry 2014
Jesse L Montgomery Carl T Wittwer

BACKGROUND Radioactive DNA polymerase activity methods are cumbersome and do not provide initial extension rates. A simple extension rate assay would enable study of basic assumptions about PCR and define the limits of rapid PCR. METHODS A continuous assay that monitors DNA polymerase extension using noncovalent DNA dyes on common real-time PCR instruments was developed. Extension rates were ...

Journal: :IEEE Photonics Technology Letters 2022

A converter from a singlemode fiber to the fundamental mode of an OM2, OM3, OM4, or OM5 type multimode is presented and used transmit 100 GbE with no detected errors over 1600 m using commercial transceivers. The based on splicing short length few-mode between fiber. designed so that has good overlap To suppress any higher order modes in fiber, optimized bend stripper used. low loss 0.35 dB, lo...

2010
Karthik S. Harve Ricky Lareu Raj Rajagopalan Michael Raghunath

Amplification of DNA in vivo occurs in intracellular environments characterized by macromolecular crowding (MMC). In vitro Polymerase-chain-reaction (PCR), however, is non-crowded, requires thermal cycling for melting of DNA strands, primer-template hybridization and enzymatic primer-extension. The temperature-optima for primer-annealing and extension are strikingly disparate which predicts pri...

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