نتایج جستجو برای: 18s rrna gene

تعداد نتایج: 1155066  

Journal: :Polar Biology 2021

Abstract The undulating ice of the McMurdo Ice Shelf, Southern Victoria Land, supports one largest networks ice-based, multiyear meltwater pond habitats in Antarctica, where microbial mats are abundant and contribute most biomass biodiversity. We used 16S rRNA 18S gene high-throughput sequencing to compare variance community structure within between ponds with different salinities pH. Proteobac...

Journal: :The Journal of eukaryotic microbiology 2003
Kathy B Sheehan Michael J Ferris Joan M Henson

An initial survey of sequences of PCR-amplified portions of the 18S rRNA genes from a community DNA clone library, prepared from an algal mat in a thermal, acidic stream in Yellowstone National Park, WY, USA, revealed among other sequences, several that matched Vahlkampfia. This finding prompted further investigation using primers specific for Naegleria. Sequences from a subsequent DNA clone li...

Journal: :international journal of molecular and cellular medicine 0
salman ghaffari parasitology and mycology group, faculty of medic+ine, babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences) narges kalantari cellular and molecular biology research centre (cmbrc), babol university of medical sciences, babol, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بابل (babol university of medical sciences)سازمان های دیگر: laboratory sciences group, faculty of paramedical, babol university of medical sciences, babol, iran. charles a hart department of medical microbiology and genito-urinary medicine, university of liverpool, liverpool, uk.

cryptosporidium is an obligate intracellular protozoan parasite infecting a wide range of hosts. the current study investigated the genetic profile of cryptosporidium species in calves in liverpool, england. fifty-two calve fecal samples were collected from a farm and initially screened by auramine phenol, modified ziehl-neelsen and elisa. pcr analysis of 18s rrna gene was carried out for the p...

Journal: :Molecular and cellular probes 2006
Ashish Mogal Sarki A Abdulkadir

In quantitative RT-PCR (qRT-PCR), analysis of gene expression is dependent on normalization using housekeeping genes such as 18S rRNA, GAPDH and beta actin. However, variability in their expression has been reported to be caused by factors like drug treatment, pathological states and cell-cycle phase. An emerging area of cancer research focuses on identifying the role of epigenetic alterations ...

Journal: :Nucleic acids research 1984
J F Connaughton A Rairkar R E Lockard A Kumar

The primary structure of rabbit 18S ribosomal RNA was determined by nucleotide sequence analysis of the RNA directly. The rabbit rRNA was specifically cleaved with T1 ribonuclease, as well as with E. coli RNase H using a Pst 1 DNA linker to generate a specific set of overlapping fragments spanning the entire length of the molecule. Both intact and fragmented 18S rRNA were end-labeled with [32P]...

2015
Jun Yang Sunny Sharma Peter Kötter Karl-Dieter Entian

Methylation of ribose sugars at the 2'-OH group is one of the major chemical modifications in rRNA, and is catalyzed by snoRNA directed C/D box snoRNPs. Previous biochemical and computational analyses of the C/D box snoRNAs have identified and mapped a large number of 2'-OH ribose methylations in rRNAs. In the present study, we systematically analyzed ribose methylations of 18S rRNA in Saccharo...

Journal: :Nucleic acids research 1994
L Holmberg Y Melander O Nygård

The secondary structure of mouse Ehrlich ascites 18S, 5.8S and 28S ribosomal RNA in situ was investigated by chemical modification using dimethyl sulphate and 1-cyclohexyl-3-(morpholinoethyl) carbodiimide metho-p-toluene sulphonate. These reagents specifically modify unpaired bases in the RNA. The reactive bases were localized by primer extension followed by gel electrophoresis. The three rRNA ...

Journal: :Nucleic acids research 1996
C L O'Day F Chavanikamannil J Abelson

We report the identification of a new gene, RRP3 (rRNA processing), which is required for pre-rRNA processing. Rrp3 is a 60.9 kDa protein that is required for maturation of the 35S primary transcript of pre-rRNA and is required for cleavages leading to mature 18S RNA. RRP3 was identified in a PCR screen for DEAD box genes. DEAD box genes are part of a large family of proteins homologous to the ...

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