Examples of 'recombinant clones' in a sentence
Meaning of "recombinant clones"
recombinant clones: This phrase pertains to genetically identical organisms formed through the process of recombination. It is commonly used in genetics, biotechnology, and molecular biology contexts
How to use "recombinant clones" in a sentence
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recombinant clones
The recombinant clones were analyzed by enzymatic digestion.
This is followed by selection and screening of recombinant clones.
The recombinant clones were studied after purification by cloning.
Molecular analysis of a sample of recombinant clones.
The positive recombinant clones were selected and analyzed by restriction.
This protocol allows one to screen large numbers of recombinant clones.
The recombinant clones were characterized by the use of restriction enzymes.
The kanomycin resistance gene allowed positive selection of recombinant clones.
All recombinant clones tested exhibited the expected pattern.
The plasmid carries an ampicillin resistance gene for selection of recombinant clones.
The recombinant clones were further characterized by restriction mapping and sequencing.
The studies indicate a very good mitotic stability of the recombinant clones.
Recombinant clones were analyzed by restriction enzyme digestion to determine insert orientation.
The heterogeneity of this subtractive library was evaluated by sequencing the recombinant clones.
Multiple recombinant clones were sequenced and the correct clones identified.
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This also introduced a BsrGI site that was used for selecting recombinant clones.
Appropriate blue recombinant clones were purified by four rounds of plaque purification.
Each strain is passaged twice in vivo to select the most stable recombinant clones.
Recombinant clones were purified by limiting dilution and dot blot hybridization.
No statistically significant differences were observed among the mucosal responses to the different recombinant clones.
Recombinant clones that showed clearing zones around the colony were isolated.
Blue / white screening of recombinant clones.
Screening of recombinant clones and analysis of expression were performed using the same protocol.
The kanamycin . resistance gene allowed positive selection of recombinant clones.
Recombinant clones were screened on solid agar medium containing sheep red blood cells.
Gene replacement had occurred in two out of the four-studied double recombinant clones.
A high proportion of the recombinant clones thereby generated contain a properly ordered insert segment.
It carries a ura3-A5 mutation which allows the selection of recombinant clones on uracil-free selective medium.
Recombinant clones were isolated and examined for expression of MIEP.
Ligations, transformation, and analysis of recombinant clones was done according Sambrook et al.
Recombinant clones were purified and their nucleotide sequence determined by Sanger method.
Figure 32, Demonstration of double recombinant clones grown on medium containing sodium deoxycholate.
Recombinant clones were identified by digestion with Hind III and by DNA sequencing.
The plasmid analysis of 11 randomly chosen recombinant clones indicates an average DNA insert of 10 kb.
Recombinant clones were screened by agar diffusion on CMC-agar.
The plasmid preparation of the recombinant clones was carried out with Biorobot 9600 Product No.
Recombinant clones were identified, plasmid DNA was isolated and subjected to DNA sequence analysis.
Four out of 400 recombinant clones were positive.
Recombinant clones containing the T7 promoter were selected using a diagnostic PCR.
Fourteen hundred TcR KmS HB101 recombinant clones were obtained.
Three recombinant clones were selected for each species and sequenced by the di-deoxy sequencing method.
Phosphodiesterases 7-11 were generated from full length human recombinant clones transfected into SF9 cells.
Therefore, only recombinant clones containing the plasmid are propagated.
Phosphodiesterases 7-11 can be generated from full length human recombinant clones transfected into SF9 cells.
In this way the recombinant clones were divided into three groups,.
The recombinant clones not permitting alpha-complementation were located from the white color of these colonies.
The sequence of some of the recombinant clones was confirmed using standard vector-based primers.
Correct recombinant clones were determined by PCR screening of bacterial cultures, and by sequencing.
The 8 identified recombinant clones have been controlled by sequencing with primer CK4.
Recombinant clones were identified as white colonies on plates containing transferrin-gal ( Yanish-Perron, supra ).
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