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peptide synthesizer gilson ams422  (Gilson Inc)


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    Gilson Inc peptide synthesizer gilson ams422
    Peptide Synthesizer Gilson Ams422, supplied by Gilson Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/peptide+synthesizer+gilson+ams422/ams+422+multiple+peptide+synthesizer/us07019112-1248-11-10
    Average 90 stars, based on 1 article reviews
    peptide synthesizer gilson ams422 - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Preventing the spontaneous modification of an HLA-A2-restricted peptide at an N-terminal glutamine or an internal cysteine residue enhances peptide antigenicity.
    Article Snippet: The p68-derived peptide, QIVDVCHDV, was identified by a reverse immunology approach as capable of reconstituting an epitope recognized by the melanoma-reactive cytotoxic T lymphocyte (CTL) line VMM5.. The peptide has not been demonstrated definitively on the cell surface by mass spectrometry; thus, it is not yet considered appropriate for use in human melanoma vaccines.. Interestingly, however, the antigenicity of this peptide was affected by spontaneous modifications at two distinct residues.

    Article Title: Peptides recognized by melanoma-specific A1-, A2- and A3-restricted cytoxic lymphocytes, and uses therefor
    Article Snippet: These peptides were synthesized by standard Fmoc chemistry using a Gilson model AMS422 peptide synthesizer.

    Article Title: Identification by Mass Spectrometry of CD8 + -T-Cell Mycobacterium tuberculosis Epitopes within the Rv0341 Gene Product
    Article Snippet: Peptides used for MS analysis were synthesized by standard 9-fluorenylmethoxy carbonyl chemistry with a Gilson AMS422 peptide synthesizer.

    Article Title: Processing, stability, and kinetic parameters of C5a peptidase from Streptococcus pyogenes.
    Article Snippet: Peptides corresponding to the COOH-terminal region of the human C5a fragment (VVASQLRANISHKDMQLGR, SQLRANISHKDMQLGR, and VVASQLRANISH) and NH2-terminal segment of the C5a peptidase (QTPDEAAE ETI and AEETIADDANDL) were synthesized as C-terminal amides on a Gilson AMS422 Multiple Peptide Synthesizer using Fmoc chemistry with pentrafluorophenyl amino acid active esters and a polyethylene glycol polystyrene support with a 5-(4¢-Fmoc-aminomethyl-3¢-5¢-dimethoxyphenoxy)valeric acid linker.

    Synthesized:

    Article Title: Mass‐spectrometric evaluation of HLA‐A*0201‐associated peptides identifies dominant naturally processed forms of CTL epitopes from MART‐1 and gp100
    Article Snippet: Jonathan C.A.. SKIPPER3, Pamela H. GULDEN2, Ronald C. HENDRICKSON2, Nancy HARTHUN1, Jennifer A. CALDWELL2, Jeffrey SHABANOWITZ3, Victor H. ENGELHARD3,5, Donald F. HUNT2,4 and Craig L. SLINGLUFF, JR.1* 1Department of Surgery, University of Virginia Health Sciences Center and Cancer Center, Charlottesville, VA, USA 2Department of Chemistry, University of Virginia Health Sciences Center and Cancer Center, Charlottesville, VA, USA 3Department of Microbiology, University of Virginia Health Sciences Center and Cancer Center, Charlottesville, VA, USA 4Department of Pathology, University of Virginia Health Sciences Center and Cancer Center, Charlottesville, VA, USA 5The Beirne Carter Center for Immunology Research, University of Virginia Health Sciences Center and Cancer Center, Charlottesville, VA, USA



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