「ASSAYS」の共起表現一覧(1語右で並び替え)
該当件数 : 72件
In receptor binding | assays, amitripylinoxide was found to have generally |
d SK2 are most sensitive for Apamin in binding | assays and physiological recordings. |
Gamma counters are used in radiobinding | assays and in radioimmunoassays (RIA). |
In addition to chemical | assays and modal mineral proportions, most QEMSCAN me |
, flow cytometry (FACS) analysis, western blot | assays, and other immunoanalytical methods. |
Due to macromolecular crowding enzyme | assays and biophysical measurements performed in dilu |
s reports of these peptides used less specific | assays and were strongly criticised as using unreliab |
ate cell growth as assessed by 3D cell culture | assays and in an orthotopic mouse tumor model by indu |
more potent than CNTF in in vitro and in vivo | assays and has improved stability properties. |
pecies, species specific, intron-exon spanning | assays and splice variant microarrays. |
These findings rely on inhibition | assays and the study of the kinetics of cleavage of t |
Such | assays are called homogenous immunoassays or less fre |
The ATPase | assays are used in two different modes: ATPase activa |
An estimated 800 million PT/INR | assays are performed annually worldwide. |
These methods, or | assays, are then used to analyze samples (plasma, tum |
Current | assays are sensitive and accurate, but require multip |
ideas were tested using sensitive and specific | assays based on a combination of HPLC and mass spectr |
ased clinical bioassays and clinical chemistry | assays, bioinformatics tools including pattern recogn |
quantify the affinity from concentration based | assays but also from the kinetics of association and |
The ATPase | assays can therefore have the potential for determini |
t available in purified form, in vitro binding | assays cannot be performed. |
fluorochromes) cells are also used, in some | assays cells get labelled during transmigration the f |
In supercoiling | assays, coiled DNA is separated in the first dimensio |
inorin A, but human tests and receptor binding | assays could not confirm this. |
Assays exceeding 1 ounce of gold per ton have been ob | |
xidation-reduction indicator in cell viability | assays for bacteria and mammalian cells. |
Several | assays for detecting ACPAs were developed in the foll |
The | assays for ROTEM analysis help to get a rapid differe |
ession pattern determined by histochemical GUS | assays in Physcomitrella patens |
An example of these | assays is again the use of the nucleotide coenzymes N |
In some | assays, it is preferable to use only the antigen-bind |
In cell-based | assays, it was found that these mutant channels aggre |
specific factor inhibitor | assays, like Protein C, TFPI, Antithrombin etc. |
specific factor | assays, like fibrin degradation products, D-dimer, th |
Other coagulation factor | assays may be performed depending on the results of a |
ent methods including RT-PCR, RNase protection | assays, microarrays, serial analysis of gene expressi |
ify the purity of a combinatorial library, but | assays need to be rapid with good resolution for all |
No-choice laboratory | assays of larval wood-boring insects from China and N |
some ions can denature certain proteins so if | assays on the function of proteins are intended then |
34,428) were shown to be active in behavioral | assays only for the ββ-isomers. |
is, for example by enzymatic or ligand binding | assays or mass spectrometry. |
Modern anti-tTG | assays rely on a human recombinant protein as an anti |
Quantitative | assays require additional calibrators with known anal |
Cell viability | assays: resazurin method, ATP test, Ethidium homodime |
Resazurin based | assays show excellent correlation to reference viabil |
In vitro chemotaxis | assays showed it to be utilized in attracting these c |
plex (snoRNP) as co-immunoprecipitation (CoIP) | assays showed that this snoRNA interacts with the sno |
Biochemical | assays showed that the +331G/A polymorphism increases |
fied when chromatin immunoprecipitation (ChIP) | assays showed that in Saccharomyces cerevisiae, even |
Although β-hematin can be produced in | assays spontaneously at low pH, the development of a |
validation of immune and protein binding based | assays such as ELISA and RIA. |
ects has revealed that in laboratory no-choice | assays, Tetrastichus attacked only actively feeding E |
A FLAG-tag can be used in many different | assays that require recognition by an antibody. |
In the double-labeled ISHs | assays, the cells were subject to fluorescence micros |
For qualitative | assays the calibrators may consist of a negative samp |
Dr. George Preti uses chemical | assays to diagnose the genetically-transmitted metabo |
The results of subsequent | assays to determine methasterone's anabolic and andro |
rs, and may interfere with the normal clinical | assays used in monitoring such disorders, and in unus |
reporter | assays using i.e. |
Luciferase, calcium signaling | assays using Coelenterazine, CFSE or Calcein |
effective buffer among the ten tested for ATP | assays using firefly luciferase. |
Since then, even more specific quantitative | assays were developed for its detection at pH 6.0. |
g the observation that when beta-galactosidase | assays were carried out at pH 6.0, only cells in sene |
Other antioxidant capacity | assays which use Trolox as a standard include the dip |
rphology, and angiogenic potential, as well as | assays which measure cell adhesion, proliferation, mi |
acroprolactin is important, as some laboratory | assays will detect it as prolactin, leading to a fals |
The resulting gene arrays and immune-response | assays will be employed to develop efficient vaccines |
on and no prolongation with incubation, factor | assays will need to be done to look for factor defici |
e potency of LSD in animal drug discrimination | assays, with the (R) isomer having an ED50 of 33nmol/ |
Co-immunoprecipitation | assays with tagged recombinant proteins showed that t |
It can also be used to perform concentration | assays without amplification or labeling typically us |
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