Examples of 'n-terminal sequencing' in a sentence
Meaning of "n-terminal sequencing"
N-terminal sequencing refers to the process of determining the amino acid sequence at the N-terminus (amino terminus) of a protein. This technique helps in identifying the first few amino acids or the starting point of a protein chain
How to use "n-terminal sequencing" in a sentence
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n-terminal sequencing
N-terminal sequencing was then performed as described above.
The sample was loaded onto a prepared glass fiber filter for n-terminal sequencing.
N-terminal sequencing is used to characterize the fusión proteins.
This material was used for N-terminal sequencing.
N-terminal sequencing of the light chain confirmed this result.
This fraction was subjected to N-terminal sequencing.
N-terminal sequencing is also used to characterize the incubated samples.
The identity of this band was confirmed by N-terminal sequencing.
N-terminal sequencing resulted in the predicted amino acid sequence.
The stained beads are then subjected to N-terminal sequencing.
N-terminal sequencing and mass spectrometry analyses allowed identification of these two halocins.
The intactness of the recombinant protein was confirmed by N-terminal sequencing.
N-terminal sequencing revealed that the optimized tPA leader was not completely cleaved.
Cleavage efficiency was confirmed by mass spectrometry and N-terminal sequencing.
N-terminal sequencing confirmed the correct amino acid sequence and cleavage of the OmpA leader.
See also
A portion of each band was used for direct N-terminal sequencing.
N-terminal sequencing has revealed the amino acid sequence ESPKALEEAPWPPPE.
The induced proteins were subjected to N-terminal sequencing to confirm their identity.
An N-terminal sequencing of this protein was then carried out, after trypsic digestion.
The degradation peptides of plasmin samples were characterized by N-terminal sequencing as follows.
N-terminal sequencing of bulk uricase preparations was done using the Edman degradation method.
The cleavage products were analyzed by N-terminal sequencing to identify the processing site.
N-terminal sequencing analysis of the purified protein revealed the sequence, APLILSRIVGG.
The specific protein was excised from the blot for N-terminal sequencing.
Subsequent N-terminal sequencing and mass spectrometry was performed to identify the specific protected peptides.
The identity of all proteins was confirmed by N-terminal sequencing and mass spectrometry.
Eldman N-terminal sequencing revealed that N-terminal end of recNgA corresponded to the expected sequence.
The actual amino-terminus of the EpiC protein was determined by N-terminal sequencing.
Attempts with N-terminal sequencing were blocked and this is consistent with the terminal modification.
The fractions eluted at each step of imidizole were pooled and analyzed by N-terminal sequencing.
Both AAA and n-terminal sequencing provided evidence of a sample of high purity and a single N-terminus.
The authenticity of the peptides were subsequently characterised by mass spectrometry and N-terminal sequencing.
N-terminal sequencing of the fractions The active heterodimer Fv fraction should contain both polypeptide chains.
The amino acid sequences of peptides were confirmed by N-terminal sequencing and mass spectrometry.
The N-terminal sequencing of the protease described by Hunfeld et al.
Samples were quality controlled using mass spectrometry, N-terminal sequencing and amino acid analysis.
N-terminal sequencing of the protein extracted from Lupinus was accomplished by Edman degradation.
The identity of the purified protein was further confirmed by mass spectrometry and N-terminal sequencing.
Sequencing of branching peptides The N-terminal sequencing procedure is standard.
The most darkly stained beads from the library are selected and subjected to N-terminal sequencing.
N-terminal sequencing N-terminal sequencing was performed by Edman degradation according to standard procedures.
The stained band was cut out from the membrane and N-terminal sequencing performed.
N-terminal sequencing was performed on an Applied Biosystems sequencer equipped with an on-line HIPC system.
Peak fractions were desalted, lyophilized and subjected to N-terminal sequencing and amino acid analysis.
The N-terminal sequencing of the TNF Inhibitory Protein gave the following amino acid sequence,.
The individual HPLC peaks were collected and the peptides identified and mapped by N-terminal sequencing.
A pyridylethylated derivative of peptide J2 suitable for N-terminal sequencing was prepared in the following fashion.
N-terminal sequencing yielded twenty residues shown in Figure 3.
Correct proteins were identified by either Mass Spec or Edman 's n-terminal sequencing.
The identity was confirmed by N-terminal sequencing of the first 15 amino acid residues.
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N-terminal sequencing was then performed as described above
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