Examples of 'solid-phase synthesis' in a sentence
Meaning of "solid-phase synthesis"
solid-phase synthesis - This term refers to a method in chemistry used to assemble molecules on a solid support, allowing for the efficient production of various compounds
How to use "solid-phase synthesis" in a sentence
Basic
Advanced
solid-phase synthesis
The classical solid-phase synthesis is preferred.
We solved this problem by using solid-phase synthesis.
Large scale solid-phase synthesis of peptides.
The oligonucleotides were prepared by standard solid-phase synthesis techniques.
The solid-phase synthesis is terminated in this manner.
The preparation is typically carried out vía a solid-phase synthesis.
Solid-phase synthesis is a common technique for peptide synthesis.
Synthesis was performed by a solid-phase synthesis method using an automatic synthesizer.
Solid-phase synthesis is a common method for synthesizing peptides.
The peptides of the invention may be synthesized by solid-phase synthesis.
Solid-phase synthesis of peptides and of their protected segments.
These compounds may be prepared by conventional solution or solid-phase synthesis.
Solid-phase synthesis is the most common technique for peptide synthesis.
The obtained resin was placed in a column for solid-phase synthesis.
This linker was used in the solid-phase synthesis of a pentapeptide as described above.
See also
These orthogonally protected cysteines are incorporated during the solid-phase synthesis of the peptide.
A versatile solid-phase synthesis strategy for preparing peptide-chelate conjugates was developed.
More specifically, the present invention relates to solid-phase synthesis of oligoribonucleotides.
An example of solid-phase synthesis of a self-complementary tag with a reactive site is shown.
This set of protecting groups is then used with standard solid-phase synthesis technology.
TIVA tags are created initially via solid-phase synthesis with the cell-penetrating peptide conjugated afterwards.
The methods of activation during coupling are also similar to those employed in solid-phase synthesis.
Further suitable cleavable linkers used in solid-phase synthesis are disclosed in Guillier et al.
The resin was introduced into a sintered column making possible the solid-phase synthesis.
The peptides were synthesized by an F-moc solid-phase synthesis method using a peptide synthesizer.
Attachment of the nucleic acid to a solid support allows synthesis using solid-phase synthesis.
In another class of embodiments, the solid-phase synthesis is Fmoc or BOC synthesis.
The method may comprise synthesizing the peptides by liquid-phase synthesis or solid-phase synthesis.
Solid-phase synthesis with Fmoc chemistry was carried out using an ABI Peptide Synthesizer.
The methods of the present invention more preferably are in an automated solid-phase synthesis format.
Solid-phase synthesis is preferred.
A wide variety of procedures exist for synthesis of peptides, solid-phase synthesis usually being preferred.
The solid-phase synthesis starts from C-terminal end of peptide.
The cost of the more advanced polymers for solid-phase synthesis is usually high.
The solid-phase synthesis starts from the C-terminal end of the compound.
The method for peptide synthesis may be either solid-phase synthesis or liquid-phase synthesis.
The solid-phase synthesis is carried out using the 2-chloro trityl chloride resin Barlos et al.
Method, Salmon calcitonin was synthesized by an ordinary procedure of solid-phase synthesis.
PNA oligomers can be prepared following standard solid-phase synthesis protocols for peptides Merrifield, B.
An aliquot ( 360 mg ) of the recovered resin was placed in a column for solid-phase synthesis.
Additional methods for solid-phase synthesis may be found in Caruthers U.S. Pat.
Background of the Invention Peptides can be manufactured by solid-phase synthesis.
Example 11, Solid-phase synthesis of thymidine decanucleotide.
The chimeric peptide immunogen is synthesized by solid-phase synthesis using Fmoc chemistry.
In one solid-phase synthesis application, the amine is covalently attached to Wang resin . [ 8 ].
The polypeptide of sequence written G 1 A is prepared by solid-phase synthesis using Boc chemistry.
Liraglutide was obtained by solid-phase synthesis with a crude peptide purity of 56 % . Sample treatment,.
The compound of any of claims 1-11, wherein the compound has been prepared by solid-phase synthesis.
The preparation of the primers by solid-phase synthesis is described in Example 1.1.
The combinatorial " split-mix synthesis " is based on the solid-phase synthesis developed by Merrifield.
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