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1 olymerized with excellent control in the DNA synthesizer.
2 erence of a conventional microwave frequency synthesizer.
3 ng phosphoramidite chemistry involving a DNA synthesizer.
4 ion of a photonic-based, microwave frequency synthesizer.
5 osition of ligands and fluorophores on a DNA synthesizer.
6 ich has already been adapted to a commercial synthesizer.
7 it into the synthesis column of a commercial synthesizer.
8 orated into oligomers using an automated DNA synthesizer.
9 e readily incorporated into DNA by automated synthesizer.
10 amidite approach in an automated solid-phase synthesizer.
11 nucleotides, using a modified maskless array synthesizer.
12 ciently to the 5'-end of DNA on an automatic synthesizer.
13 CAT)(2) on a modified Millipore Expedite DNA synthesizer.
14 e assembled into oligofluor strings on a DNA synthesizer.
15 of several oligosaccharides on a solid-phase synthesizer.
16 low cell reaction chamber connected to a DNA synthesizer.
17 a continuously streaming naturalistic speech synthesizer.
18 aptation of regular PMOs in a commercial DNA synthesizer.
19 tides using trityl-chemistry by an automated synthesizer.
20  compared to the radar's existing electronic synthesizer.
21 a fully automated flow-based oligonucleotide synthesizer.
22  acting as intracellular nanoscale molecular synthesizers.
23 portable optical atomic clocks and frequency synthesizers.
24 owever, in optical systems such as microwave synthesizers(6), optical gyroscopes(7) and atomic clocks
25 rs in an automated multiplex oligonucleotide synthesizer (AMOS).
26  oligo synthesis using this proof-of-concept synthesizer, an oligo with six nucleotide units is succe
27    Our approach requires just a conventional synthesizer and a computer-controllable optical module,
28 between DNA made on a commercially available synthesizer and this unit show that it produces DNA of s
29 chtop without the need of highly specialized synthesizers and at much lower volumes than is currently
30               Recent tools include automated synthesizers and flow reactors.
31 ened up new fields, ripe for attack by young synthesizers and theoreticians.
32 ia nanofiltration in a reactor-separator, or synthesizer apparatus where no phase or material transfe
33  we grew wild-type and a transgenic mannitol synthesizer Arabidopsis thaliana hydroponically with fre
34                      Using this custom-built synthesizer, as many as 15 reaction cycles can be perfor
35 ng oil, which were carried out on a parallel synthesizer at 160 degrees C in triplicate in a single d
36            Here, we demonstrate a heterodyne synthesizer based on ultralow-noise self-injection-locke
37 NA oligonucleotides while they remain on the synthesizer column.
38 e is a potent, mismatch-sensitive, automated synthesizer-compatible antisense S-ON modification that
39 levance in antisense therapeutics, a DNA/RNA synthesizer-compatible modular synthesis protocol of PMO
40 followed by thorough cleaning or disposal of synthesizer components.
41 igomer was synthesized in a conventional DNA synthesizer, containing neutral nucleotides with a methy
42                                    A new AGA synthesizer enables rapid temperature adjustment from -4
43  was synthesized using a solid-phase peptide synthesizer followed by rhenium cyclization.
44 rimates.(19-23) Here, we demonstrate a vocal synthesizer for birdsong, realized by mapping neural pop
45 e inherent flexibility of the maskless array synthesizer for in situ synthesis of thousands of photol
46 lity for PMO synthesis in commercial peptide synthesizers for future development.
47 irectly estimates the parameters of a speech synthesizer from all neural frequencies achieves the hig
48 ational modifications that regulate its main synthesizer, HAS2.
49   Both syntheses were performed by a peptide synthesizer in a semiautomated manner.
50 forms are generated with a two-channel field synthesizer in the infrared-visible range, with a full-w
51 ultaneous operation of two molecular peptide synthesizers in the same reaction vessel; (2) selective
52 peptide synthesis by a reconstructed peptide synthesizer is described.
53                   The generative spike-train synthesizer is trained on data from one recording sessio
54     However, CSP with commercially available synthesizers is typically limited to producing polypepti
55            Here we describe a maskless array synthesizer (MAS) that replaces the chrome masks with vi
56          This instrument, the Maskless Array Synthesizer (MAS), uses a digital light processor (DLP)
57 lly available Glyconeer 2.1 automated glycan synthesizer, monosaccharide building blocks, and a linke
58 h as a standard laboratory shaker, microwave synthesizer, or common ultrasonic bath.
59                                          The synthesizer performance is comparable to mid-range comme
60 ould harness these effects towards frequency synthesizers, phase-sensitive amplification and nonlinea
61  synthesis was carried out with an automated synthesizer platform based on a disposable Teflon-silico
62  to a DNA oligonucleotide using a custom DNA synthesizer, pooled for liquid storage, and read using a
63 been developed, including molecular muscles, synthesizers, pumps, walkers, transporters and light-dri
64 t to implement into a commercially available synthesizer, restricting access to this radiopharmaceuti
65 esign of the ELIXYS FLEX/CHEM cassette-based synthesizer supports higher temperatures and pressures t
66 crocomb-based spectroscopy, ranging, optical synthesizer, telecommunications and astronomical calibra
67 sis process is accomplished on a regular DNA synthesizer that is coupled with a UV-VIS projection dis
68 ere, we developed a touchscreen-based speech synthesizer to examine learning of speech production ind
69 ccessfully transferred into an automated DNA synthesizer to make several sequences of PMOs, demonstra
70 th tetrazole were used with an automated DNA synthesizer to prepare phosphonoacetic acid modified int
71 ctivities (CobP in aerobic adenosylcobalamin synthesizers) to convert adenosylcobinamide (AdoCbi) to
72 he reactions carried out in an automated DNA synthesizer using standard phosphoramidite chemistry.
73 d PMO-DNA chimeras have been prepared on DNA synthesizers using phosphoramidite chemistry.
74 ity and compatibility with automated DNA/RNA synthesizers utilizing controlled pore glass (CPG) as th
75                                        A DNA synthesizer was successfully employed for preparation of
76                                        A DNA synthesizer was used to construct several short ODFs car
77 ted to a standard MerMade 12 oligonucleotide synthesizer with coupling yields of 95% and has enabled
78 n developed for use in a monomodal microwave synthesizer with direct temperature control using the in
79 FETrp was synthesized on a PETCHEM automatic synthesizer with good chemical and radiochemical puritie
80  rise to ultralow-noise lasers and microwave synthesizers without the need for optical isolators, owi