نتایج جستجو برای: 2neu gene quantification

تعداد نتایج: 1215307  

2012
Wataru Yoshioka Nozomi Endo Akie Kurashige Asahi Haijima Toshihiro Endo Toshiyuki Shibata Ryutaro Nishiyama Masaki Kakeyama Chiharu Tohyama

A histoanatomical context is imperative in an analysis of gene expression in a cell in a tissue to elucidate physiological function of the cell. In this study, we made technical advances in fluorescence laser microdissection (LMD) in combination with the absolute quantification of small amounts of mRNAs from a region of interest (ROI) in fluorescence-labeled tissue sections. We demonstrate that...

Journal: :Clinical chemistry 2007
Yihong Wang Bruce Beckwith Christopher Smith Gary Horowitz

References 1. Wilhelm J, Hahn M, Pingoud A. Influence of DNA target melting behavior on real-time PCR quantification. Clin Chem 2000;46:1738–43. 2. Zuna J, Muzikova K, Madzo J, Krejci O, Trka J. Temperature non-homogeneity in rapid airflowbased cycler significantly affects real-time PCR. Biotechniques 2002;33:508–12. 3. Schneider M, Joncourt F, Sanz J, von Kanel T, Gallati S. Detection of exon ...

2014
Daniel Botman Eric Röttinger Mark Q. Martindale Johann de Jong Jaap A. Kaandorp

BACKGROUND The starlet sea anemone Nematostella vectensis is a diploblastic cnidarian that expresses a set of conserved genes for gut formation during its early development. During the last decade, the spatial distribution of many of these genes has been visualized with RNA hybridization or protein immunolocalization techniques. However, due to N. vectensis' curved and changing morphology, quan...

2013
Huali Huang Fang Cheng Ruoan Wang Dabing Zhang Litao Yang

Proper selection of endogenous reference genes and their real-time PCR assays is quite important in genetically modified organisms (GMOs) detection. To find a suitable endogenous reference gene and its real-time PCR assay for common wheat (Triticum aestivum L.) DNA content or copy number quantification, four previously reported wheat endogenous reference genes and their real-time PCR assays wer...

2014
Zhaojun Zhang Wei Wang

MOTIVATION RNA-Seq technique has been demonstrated as a revolutionary means for exploring transcriptome because it provides deep coverage and base pair-level resolution. RNA-Seq quantification is proven to be an efficient alternative to Microarray technique in gene expression study, and it is a critical component in RNA-Seq differential expression analysis. Most existing RNA-Seq quantification ...

Objective(s): Acinetobacter baumannii has a high propensity to form biofilm and frequently causes medical device-related infections with multiple-drug-resistance in hospitals. The aim of this work is to study antimicrobial resistance and the role of bap and cpaA genes in biofilm formation by A. baumannii to understand how this pathogen persists in the hospital environment. Materials and Methods...

Arash Memarnejadian, Mahdieh Soezi, Mohammad Reza Aghasadeghi, Rezvan Zabihollahi, Saeed Aminzadeh, Safieh Amini, Seyed Mehdi Sadat, Soheila Hekmat,

Background: The rapid increase of HIV-1 strains resistant to current antiretroviral drugs is a challenge for successful AIDS therapy. This necessitates the development of novel drugs, and to this end, availability of screening systems for in vitro drug discovery is a priority. Herein, we report the modification of a previously developed system for increased sensitivity, ease of use, and cost-ef...

Journal: :BioTechniques 2001
A Felske B V Pauling H F von Canstein Y Li J Lauber J Buer I Wagner-Döbler

A quantitative PCR approach is presented to detect small genomic sequence differences for molecular quantification of recombinant DNA. The only unique genetic feature of the mercury-reducing, genetically improved Pseudomonas putida KT2442::mer73 available to distinguish it from its native mercury-resistant relatives is the DNA sequence crossing the border of the insertion site of the introduced...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید