نتایج جستجو برای: 2neu gene quantification

تعداد نتایج: 1215307  

Journal: :journal of plant molecular breeding 2013
seyde mehri javadi masuod tohidfar ali haghnazari shahin negari

identification of genes with invariant levels of gene expression is a prerequisite for validating transcriptomicchanges accompanying development. ideally expression of these genes should be independent of themorphogenetic process or environmental condition.we report here the validation of internal control genei.e.tps (trehalose 6-phosphate-synthase) in cotton (gossypium spp), using taqman syste...

Journal: :Journal of clinical microbiology 2012
Jean-Marc Costa Stéphane Bretagne

Using the multicopy B1 gene and AF146527 element for the amplification of Toxoplasma gondii DNA raises the issue of reliable quantification for clinical diagnosis. We applied relative quantification to reference strains using the single-copy P30 gene as a reference. According to the parasite type, the copy numbers for the B1 gene and AF146527 element were found to be 5 to 12 and 4 to 8 times lo...

Journal: :BMC biotechnology 2016
Nicky Boulter Francia Garces Suarez Stephen Schibeci Trevor Sunderland Ornella Tolhurst Tegan Hunter George Hodge David Handelsman Ulla Simanainen Edward Hendriks Karen Duggan

BACKGROUND Research into gene expression enables scientists to decipher the complex regulatory networks that control fundamental biological processes. Quantitative real-time PCR (qPCR) is a powerful and ubiquitous method for interrogation of gene expression. Accurate quantification is essential for correct interpretation of qPCR data. However, conventional relative and absolute quantification m...

Background: Acute lymphoblastic leukemia (ALL) results from genetic alterations in a single lymphoid progenitor cell. Expression of ROR1 is reported to be increased in ALL and mantle cell lymphoma. In this study the expression of ROR1 was assessed in newly diagnosed patients with ALL.  Methods: This study was carried out on 40 patients with newly diagnosed ALL and healthy individuals as contro...

Journal: :Nucleic Acids Research 2006
James J. Yun Lawrence E. Heisler Irene I. L. Hwang Olivia Wilkins Suzanne K. Lau Martin Hyrcza Bamini Jayabalasingham Jing Jin JoAnne McLaurin Ming-Sound Tsao Sandy D. Der

Real-time quantitative PCR (qPCR) is a powerful tool for quantifying specific DNA target sequences. Although determination of relative quantity is widely accepted as a reliable means of measuring differences between samples, there are advantages to being able to determine the absolute copy numbers of a given target. One approach to absolute quantification relies on construction of an accurate s...

Journal: :Molecular and cellular probes 2002
S Fronhoffs G Totzke S Stier N Wernert M Rothe T Brüning B Koch A Sachinidis H Vetter Y Ko

Quantification of nucleic acids, especially of mRNA, is increasingly important in biomedical research. The recently developed quantitative real-time polymerase chain reaction (PCR) - a highly sensitive technology for the rapid, accurate and reproducible quantification of gene expression - offers major advantages over conventional quantitative PCR. Transcript quantification is performed in the e...

2016
Imane Abdellaoui Maane Hicham El Hadi Zineb Qmichou Abderrahmane Al Bouzidi Youssef Bakri Hassan Sefrioui Nadia Dakka Abdeladim Moumen

Prostate cancer (PCa) remains one of the most widespread and perplexing of all human malignancies. Assessment of gene expression is thought to have an important impact on cancer diagnosis, prognosis and therapeutic decisions. In this context, we explored combined expression of PCa related target genes AMACR and PCA3 in 126 formalin fixed paraffin embedded prostate tissues (FFPE) from Moroccan p...

Journal: :modares journal of medical sciences: pathobiology 2011
saeid solali saeid kaviani ali akbar movassaghpuor mohammad reza ali-parasti masoud soleimani

objective: in this study quantitative expression of mdr1 and hoct1 genes in cml patients and normal people were measured using real-time pcr. materials and methods: to study quantitative expression of these genes by real-time pcr, master-mix with syber green was used. peripheral blood samples from 30 cml patients and 27 normal persons were harvested. real-time pcr results were analyzed with re...

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