Examples of 'vector fragment' in a sentence
Meaning of "vector fragment"
Vector fragment: In the context of computer science or mathematics, a vector fragment refers to a portion or section of a vector, which is a quantity that has both magnitude and direction. It can be used in mathematical calculations, programming, or data analysis to represent a subset of a larger vector
How to use "vector fragment" in a sentence
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vector fragment
The large vector fragment was isolated.
The linearized plasmid is digested with HpaI and the vector fragment recovered.
The larger vector fragment is purified by electrophoresis as described above.
This vector is digested with NdeI and PvuII and the vector fragment is purified.
The vector fragment is isolated.
A DNA fragment is ligated to a vector fragment using a known DNA ligase.
The vector fragment was ligated to a linker oligonucleotide digested with the same restriction enzymes.
Was cut with Bgl II and Eco RI and the vector fragment was gel purified.
The vector fragment was isolated and ligated to a PCR fragment containing the CMV promoter sequence.
About 1 pmol of the vector fragment was obtained.
The vector fragment lacking the B-galactosidase gene was isolated and ligated to form pCMV.
Plasmid pBAK21 was also digested with KpnI and BamHI and the vector fragment was isolated.
The thus treated 8 kb vector fragment was then isolated from gel.
The vector fragment was combined with the EcoRI-BamHI fragment generated by PCR in step three.
Plasmid pTRKH3 is digested with EcoRV and BamHI and the vector fragment is gel-purified.
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The remaining vector fragment is purified by Geneclean and its ends re-ligated.
The DNA is treated with alkaline phosphatase and the vector fragment is gel-purified.
This vector fragment contains the AP promoter, the lamB signal, and the Tetr gene.
The resulting DNA fragment is then ligated with the vector fragment to yield plasmid pINT60.
The larger vector fragment was gel purified as described in Example 3D.
The synthesized CETP / TT insert was ligated to the CMV+ vector fragment from pCMVB.
Both the vector fragment and the insert fragment were purified, then ligated with T4 DNA ligase.
Ligation of the oligo and the vector fragment resulted in construct pIG135.
In all cases the control fragment was inserted in the pGAL1PSiST-1 vector fragment.
The Xba I - Bam HI vector fragment was isolated from pLS1 as the first ligation fragment.
After isolation the plasmid insert was ligated with the VCSM13 vector fragment.
Self-ligate the vector fragment and designate the resulting vector pBMDL1.
PBRgHuEPO was also digested with BstEII and BglII and the 6517 bp vector fragment was recovered.
The XbaI-BamHI vector fragment from pLS18 was isolated as the first ligation fragment.
The plasmid pUC19 was digested with Hin dIII and the linear vector fragment was gel-purified.
Preparation of the vector fragment from pSV2neo containing the SV40 early promoter.
PCVSVE-HBS is partially digested with SacI and the linearized vector fragment ( I ) recovered.
The PCR fragment and the vector fragment were ligated to yield construct pIG270.
Plasmid pUR2740 was digested with SacI and HindIII, and the vector fragment was isolated.
This vector fragment contains the AP promoter, the lamB signal, and the Tet ' gene.
The thus treated 4.8 kb vector fragment is then isolated from gel.
This vector fragment was ligated to the 327 bp hSOD fragment to produce plasmid pSODCF1.
The pUC19dSS vector is also digested with EcoRI and BamHI releasing a 2.0 kbp vector fragment.
The approximately 4.6 Kb vector fragment is isolated and will be referred to as Sequence B.
The linearized plasmid is then digested with AatIl and the 2931 bp vector fragment is gel-purified.
The large 6.7 kb vector fragment is isolated as described above.
The insert of pBS3-15 was determined to be a Bluescript vector fragment contaminant.
The - 2.4 kb vector fragment was purified and used in ligation.
The isolated insert was then ligated with a corresponding vector fragment derived from pPBS-ISFV-HIV-015.
The 4.4 kb vector fragment is then isolated from agarose gel.
Remove the Em-r containing fragment by isolating the vector fragment ( 3kb ) from gel.
The 2513 bp vector fragment was treated with calf intestine alkaline phosphatase.
Bam HI was added to the digest to eliminate a comigrating 1.89kb BglI-HindIII vector fragment.
The 4.5 kb vector fragment is isolated by agarose gel electrophoresis and electroelution ( fragment b ).
The CD86 containing fragment was cloned into the pEF-ADA vector fragment containing CH1.
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