「polymerase」の共起表現(1語右で並び替え)

「polymerase」の共起表現一覧(1語右で並び替え)

polymerase

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which encode their own (single subunit) RNA polymerase, a common characteristic among its members.
It is a specific inhibitor of DNA polymerase A,D in eukaryotic cells and in some viruses
thesis of cDNA, as well as DNA-dependent DNA polymerase activity that copies the sense cDNA strand i
imulates T4 polynucleotide kinase and T7 RNA polymerase activity
Pol I: implicated in DNA repair; has 5'->3' polymerase activity, and both 3'->5' exonuclease activi
imulates T4 polynucleotide kinase and T7 RNA polymerase activity, it binds to and precipitates DNA a
end as this maximizes probability of Taq DNA polymerase adding the terminal adenosine overhang.
When the polymerase advances along the DNA sequence after adding
that accumulate ahead of a translocating DNA polymerase, allowing DNA replication to continue unhind
l molecules modulating the function of human polymerase alpha which at a time modulates proliferatio
creasing the concentration of the chosen DNA polymerase also confers some resistance to polymerase-t
RNA polymerase and DNA polymerase III then replicate the si
The RNA segments are first elongated by DNA polymerase and then synthesized by primase.
aining groups (phosphotransferase, including polymerase and kinase)
quaternary structure include hemoglobin, DNA polymerase, and ion channels.
ows the sigma S factor to associate with RNA polymerase and direct the expression of the stationary
Primase is an RNA polymerase, and it can add a primer to an existing stra
fic than the direct interactions between the polymerase and the template DNA strand; because the rat
s recognised as a termination signal for RNA polymerase and the operon is not transcribed.
transferase, cis-prenyl transferase, rubber polymerase, and rubber prenyltransferase.
These primers are then extended by a DNA polymerase and a copy of the strand is made after each
These genes encode a subunit of RNA polymerase, and it is hypothesized that Lacto-rpoB RNA
genetic systematic analyses of proteins (RNA polymerase and viral coat).
inae, but do not contain a phage-encoded RNA polymerase and show greater differences at the genome o
In 1989 Science magazine named Taq polymerase as its first "Molecule of the Year".
ng primer and incubated with the enzymes DNA polymerase, ATP sulfurylase, luciferase and apyrase, an
The polymerase binds to the primer-template hybrid and begi
Structure of Taq DNA Polymerase bound to a DNA octamer
Following base excision, the polymerase can re-insert the correct base and replicati
important in order to perform PCR since DNA polymerase can act only on DNA templates.
From the hairpin loop, a DNA polymerase can then use it as a primer to transcribe a
DNA polymerase cannot add primers, and therefore, needs pri
o the Book of Mormon to multiple articles on polymerase chain reactions where he was the lead author
ortant because it produces an enzyme used in polymerase chain reaction laboratory procedures central
menon was not feasible until the 1980s, when polymerase chain reaction techniques for amplification
Polymerase chain reaction itself is the process used to
overed that this enzyme could be used in the polymerase chain reaction (PCR) process for amplifying
Hot Start PCR is a modified form of Polymerase chain reaction (PCR) which avoids non-specif
Nested polymerase chain reaction is a modification of polymera
The annealing temperature during a polymerase chain reaction determines the specificity of
STSs can be easily detected by the polymerase chain reaction (PCR) using specific primers.
are used in biochemical experiments such as polymerase chain reaction (PCR) or DNA sequencing.
CYP2D6 genotype was determined by polymerase chain reaction-restriction fragment length p
In low concentrations, it is used with polymerase chain reactions to increase yield and specif
Nonspecific primer binding obscures polymerase chain reaction results, as the nonspecific s
nzyme-Linked Immunosorbent Assay (ELISA) and polymerase chain reaction (PCR).
od samples may also be achieved by using the polymerase chain reaction (PCR).
Polymerase Chain Reaction (PCR), from a sample of blood
The target DNA undergoes the first run of polymerase chain reaction with the first set of primers
Isothermal amplification is similar to the polymerase chain reaction (PCR) but does not require th
possible the invention of a procedure called polymerase chain reaction.
been used for disposable microplates for the polymerase chain reaction (PCR) method of DNA amplifica
o replication of the damaged molecule by the polymerase chain reaction.
urora kinase B was identified in humans by a polymerase chain reaction screen for kinases that are o
Smith and Kary Mullis, who had invented the Polymerase Chain Reaction independently of Smith's work
ng amplified and quantified by a form of the Polymerase chain reaction known as Quantitative PCR or
DNA, in its genetic code, and replicates via polymerase chain reaction.
ttached to desired regions on the DNA, and a polymerase chain reaction (PCR) is employed to discover
Sodium iodide is used in polymerase chain reactions, and also (as an acetone sol
n using molecular diagnostic methods such as polymerase chain reaction (PCR).
thod for in vitro DNA amplification like the polymerase chain reaction (PCR), but that works at cons
e protein, which can then be replicated in a polymerase chain reaction to yield a significant amount
A PCR primer binding site is a site where a polymerase chain reaction (PCR) primer binds, to prime
e sequence of interest, subsequent rounds of polymerase chain reaction can be performed upon the pro
polymerase chain reaction
regions of the extracted DNA by means of the polymerase chain reaction.
ng seed tested via a grow out, sweat box, or polymerase chain reaction method to ensure that it is c
In recognition of his improvement of the polymerase chain reaction (PCR) technique, he shared th
Touchdown polymerase chain reaction or touchdown style polymerase
April: Kary Mullis discovers polymerase chain reaction (PCR).
Books @ your local library about nested polymerase chain reacitons
This pausing of the polymerase coincides with transcription of the poly-ura
ture allows gene regulatory proteins and RNA polymerase complexes to bind to the DNA sequence, which
ncodes a protein that interacts with the DNA polymerase delta p50 subunit.
Since DNA polymerase delta is involved in resynthesis of excised
DNA polymerase delta is an enzyme complex found in eukaryot
Polymerase delta-interacting protein 3 is an enzyme tha
Recently, a DNA polymerase derived from these bacteria, Bst polymerase,
e genome from a single replication fork, the polymerase DNA Pol III is the enzyme primarily responsi
Use of the thermostable Taq polymerase eliminates the need for having to add new en
An example of a core enzyme is a RNA polymerase enzyme without the sigma factor (σ).
A polymerase enzyme is used to extend the chain by adding
ociates with the promoter it affects the RNA polymerase enzyme's ability to bind and initiate transc
nds to a single amino acid change in the DNA polymerase enzyme, which is an essential enzyme for rep
atures can be prevented by using "hot-start" polymerase enzymes whose active site is blocked by an a
DNA polymerase eta (Pol η) is a eukaryotic DNA polymerase i
Polymerase eta is particularly important for allowing a
The gene encoding DNA polymerase eta is POLH, also known as XPV, because loss
idence that mutation rates (as determined by polymerase fidelity) are under selection to be neither
They also use a typical protein primed DNA polymerase for replication, a property shared with the
tion factor that affects the affinity of RNA polymerase for specific promoters on DNA
re from expression systems; particularly DNA polymerase for PCR, reverse transcriptase for RNA analy
nd to operators or promoters, preventing RNA polymerase from transcribing RNA.
pressor protein physically obstructs the RNA polymerase from transcribing the genes.
the conclusion that it was most notably the polymerase genes and the HA and NA genes that caused th
Bst polymerase has a helicase-like activity, making it able
tion by stabilizing the formation of the RNA polymerase holoenzyme enabling faster clearance of the
in which assists in the formation of the RNA polymerase holoenzyme, or may operate through a coactiv
when, in 1969, John Cairns isolated a viable Polymerase I mutant that lacked the polymerase activity
omains in the Klenow Fragment (left) and DNA Polymerase I (right).
d with transcription termination factor, RNA polymerase I or TTF1.
It is transcribed by RNA polymerase I as part of the 45S precursor that also con
DNA polymerase I comes in and fills in the correct nucleoti
DNA polymerase I removes the primer, replacing it with DNA,
cterisation, it quickly became apparent that Polymerase I was not the enzyme responsible for most DN
zyme is found as an N-terminal domain of DNA polymerase I, but some prokaryotes appear to encode a s
eing repressed, TATA-binding protein and RNA Polymerase II were still bound to the SER3 DNA in such
fically, it inhibits the assembly of the RNA polymerase II transcription complex and DNA polymerase
nd proposed to guide the modification of RNA polymerase II transcribed spliceosomal RNAs U1, U2, U4,
first person to purify and characterise DNA polymerase II and DNA polymerase III.
RNA polymerase II holoenzyme is a form of eukaryotic RNA po
r element that promotes transcription by RNA polymerase II when it is located precisely at positions
transcription factor that is part of the RNA polymerase II holoenzyme, interacts with promoters cont
DNA polymerase II (also known as DNA Pol II or Pol II) is a
transcriptase, lack LTRs, transcribed by RNA polymerase II
asal transcriptional machinery including RNA polymerase II to the promoter.
Initiation of transcription by RNA polymerase II requires the activities of more than 70 p
MED12, or mediator of RNA polymerase II trancription, subunit 12 homolog of S. ce
y subunit cyclin C are components of the RNA polymerase II holoenzyme complex, which phosphorylates
Upon ingestion, it binds to the RNA polymerase II enzyme, effectively causing cytolysis of
DNA-directed RNA polymerase II subunit RPB11-a is an enzyme that in huma
or and binds to the C-terminal domain of RNA polymerase II holoenzyme, acting as a bridge between th
The carboxy-terminal domain of RNA polymerase II typically consists of up to 52 repeats of
l transcription factors that make up the RNA polymerase II preinitiation complex.
l transcription factors that make up the RNA polymerase II preinitiation complex.
l transcription factors that make up the RNA polymerase II preinitiation complex.
ly or positively affect transcription by RNA polymerase II (Pol II).
The enzymes for capping can only bind to RNA polymerase II ensuring specificity to only these transc
An Inr for mammalian RNA polymerase II can be defined as a DNA sequence element
Upon ingestion, it binds to the RNA polymerase II enzyme which completely prevents mRNA syn
protein complex that affects eukaryotic RNA polymerase II (Pol II) transcription elongation both in
jal bodies and guide the modification of RNA polymerase II transcribed spliceosomal RNAs U1, U2, U4,
jal bodies and guide the modification of RNA polymerase II transcribed spliceosomal RNAs U1, U2, U4,
jal bodies and guide the modification of RNA polymerase II transcribed spliceosomal RNAs U1, U2, U4,
ation factor (CStF) are transferred from RNA Polymerase II to the RNA molecule.
jal bodies and guide the modification of RNA polymerase II transcribed spliceosomal RNAs U1, U2, U4,
us 35S promoter (CaMV35S), in which case RNA Polymerase II is used to express the transcript destine
02), to cause transcriptional pausing of RNA polymerase II (see MIM 180660).
T-box motifs typically present in eukaryotic polymerase II promoters.
to science include the identification of RNA polymerase II(B), the identification of transcriptional
This gene encodes a subunit of RNA polymerase II, the polymerase responsible for synthesiz
They are transcribed by RNA polymerase II, include both intron and exon, and code f
It consists of RNA polymerase II, a subset of general transcription factor
BRCA1 associates with RNA polymerase II, and through the C-terminal domain, also
eneral transcription factors, as well as RNA polymerase II, and is essential for activator-dependent
TAF9 RNA polymerase II, TATA box binding protein (TBP)-associate
nt and specific attraction to the enzyme RNA polymerase II.
amatoxins, amanullin is an inhibitor of RNA polymerase II.
hat inhibits transcription elongation by RNA Polymerase II.
matoxins, amaninamide is an inhibitor of RNA polymerase II.
er amatoxins, ε-amanitin an inhibitor of RNA polymerase II.
osphorylated carboxyl-terminal domain of RNA polymerase II; therefore it is specific to RNAs synthes
This protein forms a stable complex with RNA polymerase IIB and is required for transcriptional init
It was not until the discovery of DNA polymerase III that the main replicative DNA polymerase
As a critical component of the DNA polymerase III holoenzyme, the clamp protein binds DNA
Once priming is complete, DNA polymerase III holoenzyme is loaded into the DNA and re
The beta chain of bacterial DNA polymerase III is composed of three topologically non-e
mposed of two identical beta subunits of DNA polymerase III and hence is referred to as the beta cla
clamp (also known as β sliding clamp) of DNA polymerase III in prokaryotes.
The catalytic mechanism of DNA polymerase III involves the use of two metal ions in th
DNA polymerase III is then able to start DNA replication.
Eukaryotic 5S rRNA is synthesised by RNA polymerase III, whereas most other eukaroytic rRNAs are
6 snRNA genes , which are transcribed by RNA polymerase III, one of three major nuclear RNA polymera
o serve as a primer for DNA synthesis by DNA polymerase III.
RNA polymerase III: transcribes genes encoding tRNAs and ot
eins often bind the C-terminal domain of RNA polymerase in order to activate polymerase activity.
Pol III: the main polymerase in bacteria (responsible for elongation); ha
Cell Nuclear Antigen (PCNA) assists the DNA polymerase in the reaction, and Replication protein A (
Unlike many viruses they do not have any polymerase in the virus particle as the genome can be r
The viral polymerase incorporates these compounds with non-canoni
DNA polymerase incorporates the correct, complementary dNTP
ral product with anti-HIV activity and a DNA polymerase inhibitor.
class of antiviral drugs known as nucleoside polymerase inhibitors that was created by chemist Jerem
ative-sense genomes and so must carry an RNA polymerase inside the virion.
Hepatitis B virus DNA polymerase is a hepatitis B viral protein.
The polymerase, is a monomeric protein with two distinct fu
RNA polymerase is then used to generate long double strande
If a scanning polymerase is involved in start site selection, TFIIB m
DNA polymerase is added, which copies each fragment repeate
In biotechnology applications, T7 RNA polymerase is commonly used to transcribe DNA that has
Pfu DNA polymerase, isolated from the archean Pyrococcus furios
This polymerase lacks 3' to 5' proofreading activity and, wi
A DNA Polymerase may perform this replacement via nick transl
omains of the metaphorically hand-shaped DNA polymerase molecule.
fragments that target the 3'UTR of viral DNA polymerase mRNA.
n the coding region of the RNA-dependent RNA polymerase NS5B.
xamples include: oligomeric: hemoglobin, DNA polymerase, nucleosomes and multimeric: ion channels, m
ack) and when mutations in mitochondrial DNA polymerase occur.
stability of the open complex formed by RNA polymerase on DNA and therefore affect promoter clearan
RNAPII could affect the conformation of the polymerase on the DNA, thereby affecting subsequent sta
nd the sub-nanometer stepping motions of RNA polymerase on a DNA template.
Pol V: a Y-family DNA polymerase; participates in bypassing DNA damage.
erfering with their interaction with the DNA polymerase, PCR is inhibited.
f this enzyme class is ATP:[DNA-directed RNA polymerase] phosphotransferase.
s primers for DNA synthesis by bacterial DNA polymerase Pol III.
philic bacteria and archaea, such as Pfu DNA polymerase, possessing a proofreading activity, and are
200 adenylate residues is added by a nuclear polymerase post-transcriptionally.
be converted to positive-sense RNA by an RNA polymerase prior to translation.
reduce transcription simply by blocking RNA polymerase progression along the DNA template.

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