「PCR」の共起表現(1語右で並び替え) - Weblio英語共起表現検索

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「PCR」の共起表現一覧(1語右で並び替え)

PCR

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Allele-specific PCR: a diagnostic or cloning technique based on sin
iet overseers, he fled to Moscow in 1938, after PCR activities had been made virtually impossible b
He also criticized his own advocacy of a PCR alliance with the National Liberal Party.
mples, such as 10µg for a plasmid and 1µg for a PCR amplicon.
sphoramidite method or generated and labeled by PCR amplification or cloning (older methods).
( PCR) amplification of any sample recovered followed
Common diagnostic procedures require PCR amplification of a patient's DNA, which is easi
PCR amplification under stringent conditions is muc
fite-modified DNA that is used as templates for PCR amplification, which is subsequently hybridized
se transcription and sometimes with an optional PCR amplification.
nation of genomic libraries that are pooled and PCR amplified before sequencing.
pts) are extracted, reverse-transcribed to DNA, PCR amplified and sequenced.
ene deletion and site-specific mutagenesis with PCR and one recyclable marker
ene deletion and site-specific mutagenesis with PCR and one recyclable marker using long homologous
In this case a cDNA template is amplified by PCR and tagged with two bacteriophage-promotor sequ
ip, and a sign of cooling relations between the PCR and the Bulgarian Communist Party.
ist Party (PSR), Revolutionary Communist Party ( PCR) and Peruvian Socialist Movement (MSP).
igin, he was perceived as a local member of the PCR, and became general secretary with the depositi
damaged chromosomes at the molecular level and PCR and DNA sequencing to compare homologous gene s
mics") including patch clamp electrophysiology, PCR and immunohistochemistry.
se of Taq polymerase was the key idea that made PCR applicable to a large variety of molecular biol
xamer or random hexonucleotides are for various PCR applications such as rolling circle amplificati
A Low Cost Approach to PCR: Appropriate Transfer of Biomolecular Technique
The difference is primers used for MassTag PCR are tagged with molecules of known masses or Ma
Using TaqMan real-time quantitative PCR array methods, miRNA expression has been profil
ing GE contamination were later seen as being a PCR artifact, likely being due to contamination of
, was authored over 12 years ago, for designing PCR assays.
PCR attempts to work around the problem of ultimate
Improving PCR based detection of GMOs is a further goal of th
roduced the first commercial system for digital PCR based on integrated fluidic circuits (chips) ha
the Central Committee, which acted as the main PCR body between Congresses, had increased to 265 f
The writer had grown close to the PCR, but their relations soured ca.
on is similar to the polymerase chain reaction ( PCR) but does not require the high temperature (96°
plification like the polymerase chain reaction ( PCR), but that works at constant temperature.
have included using emulsion beads for digital PCR by Dressman and colleagues .
PCR can be used in diagnosis.
Designer, supporting the most popular real time PCR chemistries The company later came out with a p
The digital PCR concept was conceived in 1992 by Sykes et al. u
ical training) and was a participant at the Vth PCR Congress, held in Gorikovo near Moscow in Decem
However, unlike PCR, CPT does not generate multiple copies of the t
MassTag PCR demonstrated its tripartite value as a tool for
PCR dissolved in internal strife.
ious inhibitory mechanisms, to the reduction of PCR efficiency.
characteristic histological pancreatic lesion, PCR, ELISA and virus culture.
in the development included Singapore Airlines, PCR Engineers Private Limited, PCR Engineers Privat
ators, and microarray and reverse-transcriptase PCR experiments indicate that the S. coelicolor ver
In PCR experiments, the GC-content of primers are used
Better than conventional PCR for the detection of mutations in a mixed sampl
The PCR fragments that corresponded to Protocadherins w
cations block DNA polymerases and thus prevents PCR from working.
Polymerase Chain Reaction ( PCR), from a sample of blood or muscle tissue can d
imers, visible as low-molecular-weight bands on PCR gels.
Arrested that year (since the PCR had been banned in 1924), he went to the Soviet
ted Mullis's patent on the alleged grounds that PCR had been previously described in 1971.
Digital PCR has been shown to be a promising surveillance t
Digital PCR has many other applications, including detectio
he use of molecular biology techniques, such as PCR has been more and more used as a tool to measur
or his latent conflict with a large part of the PCR hierarchy.
e remained through the 1950s), infiltrating the PCR hierarchy's upper ranks.
ion to supporting conventional applications for PCR, hybridization and sequencing, NoePrimer provid
taught and a high-school dropout, he joined the PCR in 1928.
ldova), he joined the Romanian Communist Party ( PCR) in the early 1930s.
He joined the newly-outlawed PCR in 1924, and became known under his adoptive na
Analysis by 5-prime-RACE PCR indicated that the GALK1 mRNA is heterogeneous
PCR inhibitors usually affect PCR through interacti
After the outbreak of PCR inner conflicts between Ana Pauker's "Muscovite
n samples are performed with powerful Real-time PCR instrument.
Unlike normal PCR, Inverse PCR allows amplification and sequencin
his resentment of the Romanian Communist Party ( PCR) involvement.
MassTag PCR is a new technology PCR based on Mass Spectrome
Hot Start PCR is a modified form of Polymerase chain reaction
No PCR is required, which means that there will be no
MassTag PCR is a more comprehensive and sensitive diagnosti
with their interaction with the DNA polymerase, PCR is inhibited.
ns on the DNA, and a polymerase chain reaction ( PCR) is employed to discover the lengths of the sho
or expensive thermocyclers used in conventional PCR, it may be a particularly useful method for inf
-directed mutagenesis or randomly by creating a PCR library.
uipment and specific molecular biology such as: PCR machine, spectrophotometer with ultraviolet and
The trend in the PCR market was soon shifting towards a new and powe
ly reintegrated into Romania, Iacob was again a PCR member and one of its Cluj-based Regional Commi
As recorded in 1984, 90% of the PCR members were ethnic Romanian, with 7% Hungarian
microplates for the polymerase chain reaction ( PCR) method of DNA amplification.
Research is now underway to develop multiplex PCR methods that can simultaneously detect many dif
As in other real-time PCR methods, the resulting fluorescence signal perm
play, also referred to as DDRT-PCR or DD-PCR in PCR nomenclature, is the technique where a research
Similar offers were made to other parties: the PCR obtained the cooperation of Mihai Ralea, who le
Soviet sources cited PCR officials giving assurances that the respective
The limitation of performing PCR on the isolated fragments is that one must have
nd mutation containing DNA amplified by regular PCR or COLD-PCR, COLD-PCR preceding RFLP analysis w
experiments such as polymerase chain reaction ( PCR) or DNA sequencing.
Polymerase chain reaction known as Quantitative PCR or qPCR.
er plates and SPE plates and even some advanced PCR plate designs use multiple components which are
Support multiple PCR primer analysis
such as gene prediction, sequence manipulation, PCR primer design etc.
A PCR primer binding site is a site where a polymeras
It is best if the PCR primers have guanines at the 5' end as this max
could be used in the polymerase chain reaction ( PCR) process for amplifying short segments of DNA,
010, Life Technologies commercialized a digital PCR product line for the OpenArray system.
single, 3'-adenine overhang to each end of the PCR product.
As the Masscodes are liberated from PCR products they are detected with a Mass Spectrom
It is very unlikely that any of the unwanted PCR products contain binding sites for both the new
Direct visualization of PCR products, hairpins, self-dimers and false-primi
lysis - from DNA purification through robotics, PCR products, and detection to complex kits for mol
Since errors increase as PCR progresses, Pfu is the preferred polymerase whe
nes), which themselves are used as templates as PCR progresses.
r 1980, the nationalist ideology adopted by the PCR progressively targeted the Hungarian community
PCR published El Pueblo and Causa Marxista-Leninist
fer optimisation is tested and achieved through PCR, raising the question of the need to spend extr
f its members to continue political activity in PCR ranks.
es the need for having to add new enzyme to the PCR reaction during the thermocycling process.
NA, and it has been found to interfere with the PCR reaction at levels as low as 0.002 U in a 50 μL
In a standard multiplex PCR reaction, each fragment needs a unique amplifyi
In a multiplex PCR reaction, it is possible for the different sequ
samples cannot yet be achieved by HDA, whereas PCR reactions carried out in thermal cycler that ca
e taken into account when designing primers for PCR reactions.
or HDA are also relatively expensive to that of PCR reagents, more so since it comes as a ready-mad
A sequencing and the polymerase chain reaction ( PCR), require DNA primers.
Conventional PCR requires primers complementary to the termini o
ession systems; particularly DNA polymerase for PCR, reverse transcriptase for RNA analysis and res
the staff of Vasile Luca, Minister of Finance, PCR Secretary and vice-Premier in the Petru Groza c
Although a PCR section was represented at international meetin
This step is very important in order to perform PCR since DNA polymerase can act only on DNA templa
r the removal of inhibitors from samples before PCR, some DNA polymerases offer varying resistance
s improvement of the polymerase chain reaction ( PCR) technique, he shared the 1993 Nobel Prize in C
he only species of liver fluke in Thailand, but PCR techniques have revealed also Clonorchis sinens
e conversion, the genomic DNA is amplified with PCR that does not discriminate between methylated a
precise denaturation temperature control during PCR to within ± 0.3 °C (0.54 °F).
ered by Shintaro Suzuki's group, when they used PCR to find new members of the cadherin family.
The improvements made by Mullis allowed PCR to become a central technique in biochemistry a
ue to the capacity of other techniques, such as PCR, to detect specific DNA sequences from DNA samp
The ability of PCR to simultaneously amplify several loci from ind
ends and ligating the second adapter, and using PCR to specifically amplify fragments that contain
e site of the restriction endonuclease MnlI, so PCR, treatment with MnlI, and then DNA electrophore
A strip of eight PCR tubes, each containing a 100 μl reaction mixtur
The insert is created by PCR using Taq DNA polymerase.
sily detected by the polymerase chain reaction ( PCR) using specific primers.
om the gel and the eluted DNA were amplified by PCR using primers complementary to the 20 bp nonran
PCR utilizes an enzyme in T. aquaticus, now known a
and at the time of the shooting, the cops from PCR van stationed at gate number 3 had gone to sett
PCR was led by Jorge Palacios and David Benquis.
In 1984 PCR was one of three founding organizations of the
The PCR was the political wing of Lyndon Larouche's mov
hod for in vitro clonal amplification is bridge PCR, where fragments are amplified upon primers att