Supplier:
AMBEED, INC
Description:
For Research Use Only
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041386-1G , MDL Number: MFCD02682616
Supplier:
Adipogen
Description:
Potent reversible inhibitor of serine/cysteine proteases and some trypsin-like proteases. Inhibits papain, trypsin and trypsin-like serine proteases as well as cathepsin A, B and D. Similar activity spectrum comparable to leupeptin (AG-CP3-7000). Acts by forming a hemiacetal adduct between its aldehyde group and the active serine of the proteinase. Inhibits transformation of NIH3T3 cells after transfection with an activated H-ras oncogene. Used to evaluate the role of proteases in the process of malignant cell transformations. Shows antibacterial and antiparasitic activity.
Supplier:
AMBEED, INC
Description:
(S)-3-(((9H-Fluoren-9-yl)methoxy)carbonyl)thiazolidine-4-carboxylic acid, Purity: 96%, CAS Number: 198545-89-0, Appearance: Solid, Storage: Sealed in dry, 2-8 C, Size: 1g
Supplier:
Bachem Americas
Description:
Bachem additionally offers deuterated phenylalanine: Fmoc-[ring-Dâ‚…]Phe-OH B-4115.
Supplier:
AMBEED, INC
Description:
3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)pentanedioic acid, Purity: 97%, CAS Number: 247217-28-3, Appearance: Solid, Storage: Sealed in dry, 2-8 C, Size: 250mg
Supplier:
ALADDIN SCIENTIFIC
Description:
Fmoc-glycyl-glycyl-glycine
Catalog Number:
(B-3920.0005BA)
Supplier:
Bachem Americas
Description:
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Supplier:
AMBEED, INC
Description:
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(6-chloro-1H-indol-3-yl)propanoic acid 97%
Catalog Number:
(103003-348)
Supplier:
Anaspec Inc
Description:
The fibrinopeptide B is an N-terminal modified peptide with pyroglutamylation, one of the common post-translational process. After cleaving off FPA in the conversion of soluble fibrinogen to fibrin, thrombin then releases fibrinopeptide B (FPB) from the beta-chains of the fibrin I subunits to form fibrin II polymers, which associate and cross-links to form a semi-solid network, while the fibrinopeptides remain soluble in plasma. Fibrin formation associated with active thrombosis leads to significantly higher plasma levels of FPB and thus measurement of plasma FPB levels is a more sensitive and specific serologic marker for acute thrombosis.
Sequence:Pyr-GVNDNEEGFFSAR MW:1553.6 Da %Peak area by HPLC:≥95% Storage condition: -20°C
Catalog Number:
(B-3910.0005BA)
Supplier:
Bachem Americas
Description:
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Catalog Number:
(B-4085.0005BA)
Supplier:
Bachem Americas
Description:
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Supplier:
AMBEED, INC
Description:
(2S,3R)-Allyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxybutanoate, Purity: 95%, CAS Number: 136523-92-7, Appearance: Solid, Storage: Sealed in dry, 2-8 C, Size: 1g
Catalog Number:
(76983-466)
Supplier:
AMBEED, INC
Description:
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-benzylpropanoic acid, Purity: 98%, CAS number: 203854-62-0, Appearance: Solid, Storage: Sealed in dry, 2-8C, Size: 100MG
Catalog Number:
(B-3545.0005BA)
Supplier:
Bachem Americas
Description:
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
Catalog Number:
(103003-258)
Supplier:
Anaspec Inc
Description:
Melan-A is a melanocyte differentiation antigen recognized by cytotoxic T lymphocytes. This sequence is a naturally presented Melan-A/MART-1 nonamer peptide. The Melan-A/MART-1 gene is expressed by normal melanocytes, as well as by most fresh melanoma samples and melanoma cell lines. This peptide appears to be a very common immunogenic epitope for HLA-A2-restricted melanoma-specific tumor-infiltrating lymphocytes (TIL) and may be useful for the development of immunotherapeutic strategies.
Sequence:AAGIGILTV MW:814.6 Da % peak area by HPLC:95 Storage condition:-20° C
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