「electrophoresis」の共起表現一覧(2語左で並び替え)
該当件数 : 119件
Schematic representation of a protein | electrophoresis gel |
Example of AFLP Data from a Capillary | Electrophoresis Instrument |
nsferring specimens from a polyacrylamide | electrophoresis or like gel onto a membrane." |
On Agarose gel | electrophoresis, these give a characteristic "laddered" a |
ed to monitor the progress of agarose gel | electrophoresis and polyacrylamide gel electrophoresis (P |
ker to monitor the process of agarose gel | electrophoresis and polyacrylamide gel electrophoresis. |
r Semi-Denaturating Detergent Agarose Gel | Electrophoresis. |
ker to monitor the process of agarose gel | electrophoresis, running approximately at the size of a 5 |
of different lengths used in agarose gel | electrophoresis. |
Agarose gel | electrophoresis is a method used in clinical chemistry to |
w York, where he used egg albumen protein | electrophoresis to determine phylogenetic relationships i |
y (gel filtration chromatography) and gel | electrophoresis. |
NA separations by capillary and microchip | electrophoresis. |
E-cellulose chromatography and starch-gel | electrophoresis. |
a variation on the original apparatus of | electrophoresis pioneer Arne Tiselius. |
be analyzed using techniques such as gel | electrophoresis or used in recombinant DNA technology. |
first be purified by a method such as gel | electrophoresis resulting in one or a few proteins in eac |
Fluorophore assisted carbohydrate | electrophoresis or FACE is a biochemical technology suite |
They are classified on the basis of | electrophoresis and ultracentrifugation. |
conductance lithium borate polynucleotide | electrophoresis. |
ther than proteins can be separated by 2D | electrophoresis. |
Separation by capillary | electrophoresis of C-glycosylflavonoids in Passiflora sp. |
erization of Enterobacteria by Starch-Gel | Electrophoresis of Glucose-6-Phosphate Dehydrogenase and |
ilt to resolve STR fragments by capillary | electrophoresis also use fluorescent dyes to great effect |
is compatible to protein separation by 2D | electrophoresis and chromatography in multiplex experimen |
They can be visualized by gel | electrophoresis and are known individually as: U1, U2, U4 |
ion enzyme digestion are separated by gel | electrophoresis and then transferred to a membrane by blo |
s, peptides, and aminoacids, by capillary | electrophoresis and chromatography. |
are separated within a capillary by using | electrophoresis, are energized by laser light and travel |
If the DNA was resolved by gel | electrophoresis, the DNA can be visualized either by silv |
ell) and the miniplasmid by capillary gel | electrophoresis (CGE) |
be identified by using chromatography or | electrophoresis. |
the sequencing of DNA in combination with | electrophoresis. |
ving nucleic acids, the most common being | electrophoresis. |
Tricine is a commonly used | electrophoresis buffer and is also used in resuspension o |
Donnell Douglas-sponsored Continuous Flow | Electrophoresis System (CFES) experiment, using living ce |
In contrary to | electrophoresis - motion of particle in homogeneous elect |
Modern day gel | electrophoresis research often leverages software-based i |
wing fluorescent dyes for detection under | electrophoresis. |
indirect ELIS, equilibrium dialysis, gel | electrophoresis, far western blot, fluorescence polarizat |
l 0.2-1kb fragments) agarose dissolved in | electrophoresis buffer. |
plot of results from an analysis done by | electrophoresis automatic sequencing. |
microbiologist running a pulsed field gel | electrophoresis test used in bacterial typing. |
erating groups can share pulsed field gel | electrophoresis (PFGE) results which act as fingerprints |
Pulsed field gel | electrophoresis is a technique used for the separation of |
assisted flurophore-assisted carbohydrate | electrophoresis. |
used in the laboratory as buffer for gel | electrophoresis of DNA and RNA. |
in Uppsala he developed methods for zone | electrophoresis and ion exchange chromatography for hormo |
ed in the laboratory as LB buffer for gel | electrophoresis of DNA and RNA. |
en proteins as a preparatory step for gel | electrophoresis. |
nucleic acid or a protein sample from an | electrophoresis gel by applying a negative current in the |
n alkaline gel or acid gel.The hemoglobin | electrophoresis is also known to be thalessemia screening |
process known as temperature gradient gel | electrophoresis. |
mide, EtBr, is used as a DNA stain in gel | electrophoresis. |
y of migration of an analyte in capillary | electrophoresis will also depend upon the rate of electro |
ffer is a buffer solution used in agarose | electrophoresis, typically for the separation of nucleic |
n molecular biology it is used in agarose | electrophoresis typically for the separation of nucleic a |
was initially designed for use in protein | electrophoresis studies, but is currently most often used |
pectrometry, in liquid phase it is called | electrophoresis. |
proteins in the range of 1 to 100 kDa by | electrophoresis. |
etic behaviour, such as Kinetic capillary | electrophoresis (KCE), Surface Plasmon Resonance (SPR), M |
tants, as for instance in lectin affinity | electrophoresis or characterization of molecules with spe |
) and "RFU peak" refer to measurements in | electrophoresis methods, such as for DNA analysis. |
In medicine, protein | electrophoresis (a.k.a. |
first side of the biological membrane by | electrophoresis (its electrostatic attraction to the posi |
hods include the so-called mobility shift | electrophoresis, charge shift electrophoresis and affinit |
SDS-PAGE type electrophoreses, Native gel | electrophoresis does not use a charged denaturing agent. |
is procedure takes longer than normal gel | electrophoresis due to the size of the fragments being re |
he liquid separation process of capillary | electrophoresis with mass spectrometry. |
It uses the principles of gel | electrophoresis to separate out the various types of hemo |
ing a mixture of proteins by means of gel | electrophoresis, mainly in blood serum (blood plasma is n |
An electrophoretogram is the result of an | electrophoresis, which gives the movement of charged part |
were found on positions 3.3 of subsequent | electrophoresis by Moore and Perez (1967). |
On lipoprotein | electrophoresis (a test now rarely performed) it shows as |
a uniform pore size, but are optimal for | electrophoresis of proteins that are larger than 200 kDal |
ctrophoretic sequencing gels or capillary | electrophoresis have been successful in analyzing footpri |
rescence or detection by SDS PAGE protein | electrophoresis. |
a denaturing agent in polyacrylamide gel | electrophoresis. |
sodium dodecyl sulfate polyacrylamide gel | electrophoresis, commonly used to analyse proteins |
Polyacrylamide gel | electrophoresis (PAGE) is used for separating proteins ra |
it intestinal mRNA with a preparative gel | electrophoresis device developed by Hediger. |
r ligand-binding proteins, onedimentional | electrophoresis similar to counter electrophoresis or to |
b can be removed and the gel is ready for | electrophoresis. |
he way that electro-osmosis is reverse to | electrophoresis. |
weights are 74,000 and 55,000 per SDS gel | electrophoresis. |
bunit monomers via SDS-polyacrylamide gel | electrophoresis. |
cell membranes by SDS-polyacrylamide gel | electrophoresis and staining with periodic acid-Schiff st |
Proteins are separated by | electrophoresis, then antibodies are applied in a trough |
Serum protein | electrophoresis showing a paraprotein (peak in the gamma |
n assay in combination with serum protein | electrophoresis and serum immunofixation electrophoresis |
electric field, which makes it similar to | electrophoresis. |
ysis of proteins from the two species, by | electrophoresis, also supports their separation into two |
the voltage can be increased to speed up | electrophoresis so that a gel run takes only a fraction o |
the voltage can be increased to speed up | electrophoresis so that a gel run takes only a fraction o |
he moving-boundary method of studying the | electrophoresis of proteins. |
sodium dodecyl sulfate-polyacrylamide gel | electrophoresis (SDS-PAGE) it showed a mass of 80 kDa4. |
bulins and is more expensive than protein | electrophoresis. |
hemically or acrylamidated during the gel | electrophoresis. |
y electrophoretic mobility due to the gel | electrophoresis mechanism. |
ngineering technology, from the capillary | electrophoresis units used in large-scale DNA sequencing |
The Gel | electrophoresis working group also focuses on image analy |
or Southern blot analysis because the gel | electrophoresis followed by transfer to a membrane will s |
so PCR, treatment with MnlI, and then DNA | electrophoresis will give a diagnosis. |
h.D. in Uppsala 1957 with the thesis Zone | electrophoresis in columns and adsorption chromatography |
ied, they are resolved either through gel | electrophoresis or capillary electrophoresis, which will |
communications satellites, and to perform | electrophoresis and echocardiograph operations in space i |
on of surfactant to traditional capillary | electrophoresis instrumentation has dramatically expanded |
Two-dimensional gel | electrophoresis, abbreviated as 2-DE or 2-D electrophores |
Two-dimensional gel | electrophoresis, a specific type of gel electrophoresis c |
es and structures and two-dimensional gel | electrophoresis (2-D Page electrophoresis). |
ixer, complete equipment for each type of | electrophoresis, bloteri, visualization system of gels an |
For specific types of | electrophoresis (for example, the process of administerin |
Typically the | electrophoresis gel is stained with Coomassie Brilliant B |
Before the widespread use of | electrophoresis gels, protein electrophoresis was perform |
BE can be diluted to 0.5X prior to use in | electrophoresis, 1x is acceptable as well. |
ractions can be quantitated using protein | electrophoresis, but the total protein test is a faster a |
ered followed by sequencing via Capillary | electrophoresis in order to obtain a DNA profile which ca |
netic variation in Drosophila via protein | electrophoresis, the theoretical results from the infinit |
technique should not be confused with gel | electrophoresis, where an electric field is used to "pull |
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