Q(Trt)-N(Trt)-T(tBu)-L-K(Boc)-A-T(tBu)-NH
O
O
Fmoc-NH
O
Fmoc-SPPS
Sieber resin
04-64-0059
O
P-K(Boc)-Y(tBu)-V-K(Boc)-Q(Trt)-N(Trt)-T(tBu)-L-K(Boc)-A-T(tBu)-NH
O
O
O
NovaPEG FMPB resin
01-64-0472 NovaPEG amino resin hydrochloride 1 g
5 g
25 g
01-64-0474 NovaPEG Wang resin 1 g
5 g
25 g
01-64-0473 NovaPEG Rink Amide resin 1 g
5 g
25 g
01-64-0477 NovaPEG FMPB
01-64-0470 Rink Amide AM resin LL (100 - 200 mesh) 1 g
NEW 5 g
25 g
01-64-0471 Wang resin LL (100 - 200 mesh) 5 g
NEW 25 g
100 g
04-12-2074 Fmoc-Ala-Wang resin LL 1 g
NEW
polystyrene 8 loaded with
Pd(0) (Method 1) was chosen as the catalyst for this study,
since in comparative tests (Method 2) with supported
triphenylphosphine polystyrene 9 (01-64-0308),
diphenylphosphinomethyl
ProbeLibrary probes using the LightCycler® 2.0
Instrument.
6,0E+04
5,0E+04
4,0E+04
3,0E+04
2,0E+04
1,0E+04
0,0E+04
A
cc
ur
ac
y
Transcriptor
High Fidelity
Reverse
Transcriptase
, and Yanagita, M., J. Biochem.,
62(6), 633-641 (1967).
13. Narahashi, Y. et al., J. Biochem., 64(4), 427-437
(1967).
14. Narahashi, Y., and Yoda, K., J. Biochem., 73(4),
831-841 (1973).
with sensitive detection.
• Serum, plasma, and urine samples require a 64-
fold dilution in 50 mM phosphate. A suggested 64-
fold dilution is 5 µL of sample + 315 µL of Sample
Diluent.
Reagent
method for identifying bacterial enzymes. J. Clin.
Pathol., 28(8), 686-687 (1975).
MES/CRF 1/04
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