Examples of 'recognition sites' in a sentence
Meaning of "recognition sites"
Recognition sites are specific regions on DNA or RNA molecules where certain proteins or enzymes can bind. These sites are essential for various biological processes, such as DNA replication, transcription, and gene expression. Recognition sites play a crucial role in molecular biology research and genetic engineering.
How to use "recognition sites" in a sentence
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recognition sites
Recognition sites of many restriction enzymes are palindromic.
Homing endonuclease recognition sites are extremely rare.
A nucleotide sequence representing restriction enzyme recognition sites.
Restriction enzyme recognition sites are indicated by name.
Comparing triplets with different glycosidase recognition sites.
The recognition sites of the meganucleases are not palyndromic.
Arranging the glycosidase recognition sites.
Restriction enzyme recognition sites are indicated by name and by underlining.
The relative positions of restriction endonuclease recognition sites are indicated.
The recognition sites must be modified so that insulin can be recognized.
The used AgeI and BamHI recognition sites are underlined.
Recognition sites are also referred to in the art as recognition target sites.
Exemplary restriction enzyme recognition sites have been indicated previously.
This can involve one or more recombinase recognition sites.
The restriction endonuclease recognition sites are designated by the raised boxes.
See also
Multiple restriction sites can be the same or different recognition sites.
The recognition sites of the restriction enzymes are either completely or partially asymmetric.
The positions of the main restriction enzyme recognition sites are indicated.
The recognition sites for some restriction enzymes are indicated by standard abbreviations.
This linker introduced further unique restriction enzyme recognition sites.
None of the said first or second recognition sites may be located in área b.
Some recognize palindromic sequences while others have asymmetric recognition sites.
Restriction enzyme recognition sites used in assembly of each chimeric cDNA are indicated.
These compounds have only a negligible affinity for benzodiazepine recognition sites.
All these recognition sites come within the scope of the present invention.
Each recombinable unit comprises one or more internal recombinase recognition sites.
A few key restriction enzyme recognition sites and their map positions are shown.
A further alternative relies on the specificity of metabolic enzymes for their recognition sites.
A special linker that provided unique recognition sites was placed into this vector.
Other sequence changes may be desired in order to introduce restriction enzyme recognition sites.
Some collagen type peptides containing cellular recognition sites were grafted onto those extremities.
The recognition sites for several restriction endonucleases are shown above the nucleotide sequences.
Active variants and fragments of the exemplified recognition sites are also provided.
Native recognition sites for BbvI are inactivated by first treating the target polynucleotide by methylation.
Restriction enzymes are positioned over their own recognition sites on the illustrations.
Two recombinase recognition sites are placed in the desirable gene expression cassette in opposite orientations.
The sequences of the primers are modified to provide recognition sites for restriction enzymes.
The recognition sites for different restriction enzymes are indicated above and beneath the sequence.
Molecular imprinting is a technique used for creating selective recognition sites in synthetic polymers.
A molecule of IgM carries ten recognition sites whereas a fimbria certainly carries a lot more.
A suitable host cell comprises one or more suitable recombinase recognition sites in its genome.
There are a limited number of recognition sites within a vector for any particular restriction enzyme.
The amplified or synthesized fragments have specific restriction endonuclease recognition sites at the ends.
Primers containing the recognition sites for the nicking restriction enzyme drive the exponential amplification.
In certain embodiments the tag section may comprise recognition sites for restriction endonucleases.
Lysine residues provide recognition sites for trypsin and tyrosine residues provide recognition sites for chymotripsin.
The capture agent and the detection agent may have identical antigen recognition sites.
Meganucleases can be used to cleave meganuclease recognition sites within the coding regions of a polynucleotide.
Recognition sites for DNA restriction enzymes used for cloning are underlined.
The results provide further evidence for specific cellular and membrane recognition sites for barbiturate action.
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