Examples of 'vector using' in a sentence

Meaning of "vector using"

vector using - referring to a mathematical concept where a quantity is represented by magnitude and direction. It is commonly used in physics and engineering to depict forces or velocities

How to use "vector using" in a sentence

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vector using
It is then possible to code a given network vector using a product code.
A universal chloroplast vector using corn chloroplast DNA is constructed as follows.
It is then possible to code a given lattice vector using a product code.
Coded motion vector using the predicted vector, the motion vector.
Various sgRNA sequences were cloned into this vector using isothermal assembly.
A vector using the GAL4-inducible USA promoter is pUAST.
The primer was ligated into the vector using standard ligation procedures.
These are genes generally required for the construction of a vector using E. coli.
These can be introduced into the expression vector using introduced or natural restriction sites.
Various methods can be used in order to evaluate the speed vector using imaging methods.
G and 20 µg of transfer vector using Lipofectamine+ following the manufacturer 's instructions ( Invitrogen ).
This particular embodiment makes it easier to calculate the velocity vector using the measurements.
The Ori sequence is reinserted in the vector using two joiner oligos and isothermal assembly.
The above molecules can be assembled, isolated and cloned into a suitable vector using known techniques.
Alternative estimation of the direction of arrival vector using complex receiver-specific information,.

See also

PCR products were subsequently cloned by substitution into the pVenv4 vector using standard methods.
The product was cloned into the pIRES-Hyg vector using NsiI and NotI restriction enzymes.
The amplified VEGI-alpha coding sequence was ligated into the purified pCl vector using T4 DNA ligase.
Function, Normalize the VQ target vector using the predicted excitation gain.
These nucleic acid sequences are inserted into an appropriate expression vector using standard ligation techniques.
Relatedness is determined by comparing the gloss vector using the Cosine similarity measure.
The fragments are then inserted into the vector using DNA ligase.
One suitable method involves producing a new vector using the techniques described in Example 1.
All ORF containing fragments were ligated into the linearized vector using T4 ligase.
The PCR product was cloned into pQe30 expression vector using BamHI and HindIII restriction sites.
The aforementioned DNA was ligated to the EcoRI-digested site of the vector using a T4 DNA ligase.
The decoding unit 504 decodes the current motion vector using the selected predicted motion vector.
Such polynucleotides can be inserted into an appropriate expression vector using standard ligation techniques.
The PCR products were cloned into a pET based expression vector using conventional restriction / ligation methods.
For example, a polynucleotide may be incorporated into a viral vector using well known techniques.
The DNA segments were incorporated in an expression vector using the scheme outlined in Figure 6.
Using the processor means to calculate the norm of said anomaly vector using a Mahalanobis distance,.
MDA-435 cells were transfected with either vector using the standard calcium phosphate method.
The calculated depth value is later converted into a disparity vector using equations ( 1 ) and ( 2 ).
A cDNA library is constructed in a yeast expression vector using mRNA obtained from rice plants.
Alternatively, the PCR product is directly cloned into a suitable vector using for example TA cloning.
Step 500 executes by estimating a line track state vector using a linear Kalman filter state estimation.
The protomers were prepared in an E. coli plasmid vector using standard techniques.
The LC-linker is cut out from the pCR 4 cloning vector using BamHl / Psfl restriction enzymes digests.
The nucleotide sequences are cloned into a Pichia expression vector using standard molecular techniques.
We recently created macaque combinatorial libraries in our pMS vector using these optimized PCR conditions.
Each synthetic oligonucleotide was then cut from the vector using Fok I restriction endonuclease.
The FLAG-tagged fusión genes were assembled in a pALTERMAX vector using conventional molecular techniques.
Production of a huFactor VIII-expressing vector using the TRIP system.
FIG . 6 shows the reconstruction of the depolarization vector using the above two phase shifts.
The fragment was then cloned into the pAILo2 expression vector using an Infusion Cloning Kit.
The fragment was then cloned into the pAlLo2 expression vector using an Infusion Cloning Kit.
Then these purified fragments were ligated to the pGEM-T Vector using the corresponding Promega Kit,.
A full length CD28 molecule was cut from the TA cloning vector using flanking EcoRI sites.
Fig . 34 is an example of a method for determining a motion vector using reference indices.

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