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1  to a sigma phase was observed by increasing annealing temperature.
2 structure can be easily controlled by tuning annealing temperature.
3 erials, which was more prominent at elevated annealing temperature.
4  continuously decreased with the increase of annealing temperature.
5 the magnetic interaction is dependent on the annealing temperature.
6 istors, has strong performance dependence on annealing temperature.
7 decreasing the amount of Ag and lowering the annealing temperature.
8 s its melting temperature below the reaction annealing temperature.
9 and selects the primer pairs with comparable annealing temperature.
10 11) substrate, and facet sizes increase with annealing temperature.
11 e in length, base composition, location, and annealing temperature.
12 y reducing the sample input and lowering the annealing temperature.
13 rimer, the low T m flanking primer and a low annealing temperature.
14 he Kondo effect is more pronounced at higher annealing temperature.
15 e than the samples quenched at 600 degrees C annealing temperature.
16 fects were largely overcome through elevated annealing temperature.
17 ant for cryoprotection, as a function of the annealing temperature.
18 nt on the solution reaching denaturation and annealing temperatures.
19 ent, deriving CODEHOPs and calculating their annealing temperatures.
20 harmacogenetics for templates with different annealing temperatures.
21 ers in a DNA cycle sequencing system at high annealing temperatures.
22 fication, most likely due to unavoidable low annealing temperatures.
23 res but remains relatively constant at lower annealing temperatures.
24 ies of substitutions quenched from different annealing temperatures.
25  accelerated annealing time (8 h) and higher annealing temperature (155-175 degrees C).
26                               The changes in annealing temperature (~450 degrees C, ~850 degrees C an
27                            The effect of the annealing temperature (700, 800, or 900 degrees C) on th
28 ll nanoliter qPCR (nL-qPCR) chip at a single annealing temperature and buffer condition.
29 ent a robust fundamental correlation between annealing temperature and catalytic activity, where a ap
30  heterojunctions, or alloys depending on the annealing temperature and composition.
31 an be improved 4- to 10-fold by lowering the annealing temperature and implementing a reverse transcr
32  rate of 1.5 degrees C s(-1) for reaching an annealing temperature and is run for 48 cycles.
33 ike micelles, and finally spherulites as the annealing temperature and supersaturation degree are inc
34 ed nanoparticle superlattices is dictated by annealing temperature and the flexibility of the interpa
35  found that, the growth rate scales with the annealing temperature and the graphene height is proport
36  associated hyperspace, spanning processing (annealing temperature and time), material (composition a
37  skutterudite superlattices as a function of annealing temperature and time.
38         The cation ordering is controlled by annealing temperature and when present it also polarises
39  combinations of magnesium concentration and annealing temperature, and after screening over 750 mark
40  a function of the ratio of organic content, annealing temperature, and substrate surface characteris
41 4H-SiC (0001) by the systematic variation of annealing temperature (AT) with several deposition amoun
42 uction only for samples quenched from higher annealing temperatures but remains relatively constant a
43 We introduce quantitative correlations among annealing temperature, CSRO, and nano-hardness and elect
44  and probes, a thermal gradient with varying annealing temperatures, different primers/probe concentr
45                    The program estimates the annealing temperature for each primer and selects the pr
46 primer combinations, used with the optimized annealing temperature for each set of primers, produced
47 hole-transport layers, caused by the limited annealing temperature for f-PSMs, severely disrupt the f
48                       We predict the optimal annealing temperatures for the formation of VVs at high
49 ssence of the method is to use two different annealing temperatures in consecutive PCR cycles to effe
50 ly due to high primer concentrations and low annealing temperatures in this protocol.
51 mensional hierarchical morphologies when the annealing temperature increased to 900 degrees C.
52 and the substrate due to the high growth and annealing temperatures involved in the LPE technique.
53 his quantitatively shows that an increase in annealing temperature leads to a reduction in copper vac
54 ees C, much lower than the standard FAPbI(3) annealing temperature of 150 degrees C.
55 articular, the MnRuO(x)-300 catalyst from an annealing temperature of 300 degrees C contains an optim
56 p product was amplified differentially at an annealing temperature of 56 degrees C but not with the t
57 ow temperature to 1.5 eV at the experimental annealing temperature of 573 K.
58            The first PCR was performed at an annealing temperature of 68 degrees C, which did not all
59 e processing (printing) and post-processing (annealing) temperature of the metal patterns must be low
60 s were tested for HIV-1 DNA by using a lower annealing temperature or a different primer pair for the
61 quency was unaffected by a change in primer, annealing temperature or amount of DNA input.
62  HIV-1 DNA sequences by using a 50 degrees C annealing temperature or the pol primer pair were 71 and
63 n abrupt mobility change, so that at typical annealing temperatures, polycrystals will contain both s
64 -ray reflectivity collected as a function of annealing temperature provided information on lateral an
65  the resulting GNRs can be controlled by the annealing temperature, providing GNR films with optical
66 sults show that small changes in the thermal annealing temperature result in significant changes to t
67 examines the effect of fragmentation length, annealing temperature, sequence identity and number of s
68 3+)]/[In(3+) + Sn(4+)] molar ratio (0.7) and annealing temperature (T(a) = 250 degrees C) afford TFTs
69 e polymerase enzymes (n = 2); (3) the primer annealing temperature (T(a)) specified for the used poly
70  have been developed, but these require high annealing temperatures (T(anneal)>400 degrees C), which
71     More interestingly, with the increase of annealing temperature, the crystallinity of the Ni shell
72                                  At a higher annealing temperature, the quasi-1D chain structure tran
73                             Despite the high annealing temperatures, the average grain size was maint
74 lations and merge the modal by adjusting the annealing temperature to locate the promising basins.
75 onducting transition strongly depends on the annealing temperature used.
76 amplify the expected size product at a lower annealing temperature using the OCP2 3'-UTR PCR primers
77 P multiplexing and dissecting the effects of annealing temperature, VTM interference, and inoculum vo
78                                     When the annealing temperature was increased to 800 K, electron d
79 centage of primers/probes bound at the assay annealing temperature was performed to assess the potent
80 ercentage of bound primer/probe at the assay annealing temperature was performed to assess the potent
81 he qPCR conditions, primer concentration and annealing temperature, were optimized.
82 n limited agglomeration at comparatively low annealing temperature, which is also accompanied with th
83 gaprimer product of the first PCR and a high annealing temperature, which prevents priming by the low
84                        The optimized thermal annealing temperature window and preferred temperature d
85 erage length of the cylinders increases with annealing temperature, with a narrow length distribution