Fluorenes
Chem-Impex International, Inc. Fmoc-L-azetidine-2-carboxylic acid | 136552-06-2 | MFCD01320843 | 1G
Fmoc-L-azetidine-2-carboxylic acid, 136552-06-2, MFCD01320843, 1G
Chem-Impex International, Inc. Fmoc-isothiocyanate | 199915-38-3 | MFCD01861169 | 5G
Fmoc-isothiocyanate, 199915-38-3, MFCD01861169, 5G
Chem-Impex International, Inc. Fmoc-L-norvaline | 135112-28-6 | MFCD00155631 | 5G
Fmoc-L-norvaline, 135112-28-6, MFCD00155631, 5G
Sigma Aldrich Fine Chemicals Biosciences Monoclonal Anti-Digoxin-Biotin antibody produced in mouse clone DI-22, purified immunoglobulin, buffered aqueous solution | 0.5ML
Monoclonal Anti-Digoxin-Biotin antibody produced in mouse clone DI-22, purified immunoglobulin, buffered aqueous solution | 0.5ML
Sigma Aldrich Fine Chemicals Biosciences Monoclonal Anti-Digoxin-Biotin antibody produced in mouse clone DI-22, purified immunoglobulin, buffered aqueous solution | 0.2ML
Monoclonal Anti-Digoxin-Biotin antibody produced in mouse clone DI-22, purified immunoglobulin, buffered aqueous solution | 0.2ML
MilliporeSigma FMOC-PHG-OH
Fmoc-Phg-OH; > /=98% by TLC and HPLC; Solid; EMD; Novabiochem; 5g; N-alpha-Fmoc-L-phenylglycine; F.W. 373.4; C23H19NO4; CAS: 102410-65-1
Chem-Impex International, Inc. Fmoc-L-citrulline | 133174-15-9 | MFCD00151943 | 5G
Fmoc-L-citrulline, 133174-15-9, MFCD00151943, 5G
Chem-Impex International, Inc. Fmoc-Dab(N3)-OH | MFCD11052920 | 100MG
Fmoc-Dab(N3)-OH, MFCD11052920, 100MG
MilliporeSigma FMOC-SAR-OH
Fmoc-Sar-OH; > /=98% by TLC and HPLC; Solid; EMD; Novabiochem; 5g; N-alpha-Fmoc-sarcosine; F.W. 311.3; C18H17NO4; CAS: 77128-70-2
AnaSpec FMOC-(2S, 4R)-(-)-4-T-BUTOXYPY
Fmoc-(2S,4R)-(-)-4-t-butoxypyrrolidine-2-carboxylic acid[Fmoc-trans-4-t-butoxy-L-proline] ; MW 409.5; M.F. C24H27NO5 (5 g)
AnaSpec FMOC-LYS(N3)-OH 250MG
Fmoc-Lys(N3)-OH[Fmoc-azidolysine; Fmoc-lys(azide); Fmoc-lysine azide] ; MW 394.42; M.F. C21H22N4O4 (250 mg) An unusual amino acid used in Solid Phase Peptide Synthesis (SPPS) for the synthesis of side-chain modified peptides and proteins.1 The side-chain azido (N3) group is stable in trifluoroacetic acid (TFA) or piperidine (Pip), two reagents commonly used in SPPS. The azido group can be readily converted to an amine on the solid phase or in solution via the Staudinger reduction.2