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You Searched For: N-Boc-glycine+(Boc-Gly-OH)


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Boc-Thr(Ile-Fmoc)-OH

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Image Unavailable-B-3975.0005BA

Boc-Thr(Leu-Fmoc)-OH

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Image Unavailable-TCB3178-1G

(2S,4S)-1-(tert-Butoxycarbonyl)-4-fluoro-2-pyrrolidinecarboxylic acid ≥97.0% (by GC, titration analysis)

Supplier: TCI America
Description: CAS Number: 203866-13-1
MDL Number: MFCD04973957
Molecular Formula: C10H16FNO4
Molecular Weight: 233.24
Purity/Analysis Method: >97.0% (GC,T)
Form: Crystal
Melting point (°C): 162
Specific rotation [a]20/D: -57 deg (C=1, MeOH)

SDS

Product Image-77525-790

Gly (Glycine) ELISA Kit

Catalog Number: (77525-790)
Supplier: AFG Bioscience
Description: Gly (Glycine) ELISA Kit
Product Image-77526-854

Rat Gly (Glycine) ELISA Kit

Catalog Number: (77526-854)
Supplier: AFG Bioscience
Description: Rat Gly (Glycine) ELISA Kit
Image Unavailable-E-1970.0005BA

Benzyl-2-aminoacetate

Supplier: Bachem Americas
Description: Sequence: H-Gly-OBzl · HCl

Image Unavailable-TCB4184-5G

Nδ-(tert-Butoxycarbonyl)-Nɑ-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-ornithine ≥98.0% (by HPLC, titration analysis)

Catalog Number: (TCB4184-5G)
Supplier: TCI America
Description: CAS Number: 109425-55-0
MDL Number: MFCD00065668
Molecular Formula: C25H30N2O6
Molecular Weight: 454.52
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 134
Specific rotation [a]20/D: -9 deg (C=1, DMF)
Storage Temperature: 0-10°C

SDS


Product Image-77511-114

Human Gly (Glycine) ELISA Kit

Catalog Number: (77511-114)
Supplier: AFG Bioscience
Description: Human Gly (Glycine) ELISA Kit
Image Unavailable-B-3930.0005BA

Fmoc-Lys(Boc)-Thr(Psi(Me,Me)pro)-OH

Catalog Number: (B-3930.0005BA)
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.
Image Unavailable-B-4295.0005BA

Fmoc-Lys(Boc)-Ser(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4295.0005BA)
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.
Image Unavailable-B-4315.0005BA

Fmoc-Trp(Boc)-Ser(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4315.0005BA)
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.
Image Unavailable-B-4320.0005BA

Fmoc-Trp(Boc)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4320.0005BA)
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.
Image Unavailable-E-1965.0025BA

2,5-Piperazinedione

Catalog Number: (E-1965.0025BA)
Supplier: Bachem Americas
Description: Also known as Cyclo(-Gly-Gly), dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.
Image Unavailable-TCC2838-25G

N-Carbobenzoxyglycine methyl ester ≥95.0% (by GC)

Supplier: TCI America
Description: CAS Number: 1212-53-9
MDL Number: MFCD00043631
Molecular Formula: C11H13NO4
Molecular Weight: 223.23
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Boiling point (°C): 151
Specific Gravity (20/20): 1.19

SDS

Image Unavailable-MSPP-212305

Anti-G4S Linker Rabbit Monoclonal Antibody [clone: S13] (PE (Phycoerythrin))

Supplier: CYTOART, INC. MS
Description: This antibody reacts with cell membrane-expressed CARs of varying specificity containing a G4S linker within the scFv of the extracellular domain. The poly-Glycine-Serine (G4S) linker is a kind of synthetic peptide linker sequence that is flexible and unstructured. It is frequently used to link the variable heavy (VH) domain and the variable light (VL) domain of single-chain variable fragments (scFvs) and chimeric antigen receptors (CARs) that have an extracellular domain scFv for recognizing target antigens. The linker is made up of a core pentapeptide sequence, Gly-Gly-Gly-Gly-Ser.

New Product

Image Unavailable-MSPP-212302

Anti-G4S Linker Rabbit Monoclonal Antibody [clone: S13] (Alexa Fluor® 647)

Supplier: CYTOART, INC. MS
Description: This antibody reacts with cell membrane-expressed CARs of varying specificity containing a G4S linker within the scFv of the extracellular domain. The poly-Glycine-Serine (G4S) linker is a kind of synthetic peptide linker sequence that is flexible and unstructured. It is frequently used to link the variable heavy (VH) domain and the variable light (VL) domain of single-chain variable fragments (scFvs) and chimeric antigen receptors (CARs) that have an extracellular domain scFv for recognizing target antigens. The linker is made up of a core pentapeptide sequence, Gly-Gly-Gly-Gly-Ser.

New Product

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