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1 hat is compatible with a standard laboratory incubator.
2 image cell cultures directly from within an incubator.
3 revalent in vivo as they appear to be in the incubator.
4 track cell culture growth directly within an incubator.
5 hemical exposures was via a modified culture incubator.
6 on was 1.7%, 3-fold less than other reported incubators.
7 ted fluorescence imaging of cell cultures in incubators.
8 of a custom-built, demountable, microfluidic-incubator and a FTIR microscope coupled to a focal plane
12 birth, Sprague-Dawley rats were placed into incubators and exposed to an atmosphere alternating betw
13 grants, friends and family, angel investors, incubators and industry partners from the perspective of
18 pective detection instruments and a standard incubator at 37 degrees C, with TTD and CFU being monito
19 ) were heat-stressed in a prewarmed neonatal incubator at 44-47 degrees C until systolic blood pressu
22 1.5 T system with the use of a Nomag IC 1.5 incubator by Lammers Medical Technology Co., equipped wi
24 wn at various densities in standard in vitro incubator conditions do not have different pericellular
25 OWLS cuvette to be operated as a 1.5 ml mini-incubator, controlling both temperature and CO2 levels.
27 t limited to brain scans, with the use of an incubator equipped not only with head coil, but also wit
32 investigated in a temperature gradient block incubator for temperatures ranging from -1 to 40 degrees
34 were constructed and allowed to mature in an incubator in a facility approved for human-tissue manufa
35 microg/mL) and transferred to a pressurized incubator in which 30 mm Hg of pressure was applied for
38 )Luer to allow for a convenient, sterile and incubator-independent time-lapse microscopic observation
39 hocytes are almost always conducted in CO(2) incubators maintained at atmospheric oxygen levels (atmo
43 nation of warm, humid conditions in neonatal incubators, particularly in association with occlusive d
44 Dedicated neonatal coils integrated with the incubator permit more accurate diagnosis than the previo
46 In an approach to this problem, we provided incubator-reared bees with opportunities to fly and see
47 rmia (CN) by placement in a servo-controlled incubator set to maintain rectal temperature at 37.4 deg
51 nature, and the setup was kept in a standard incubator under controlled conditions during the measure
52 ty of images obtained with the MR-compatible incubator was superior to that of images obtained with t
53 development: does the gut serve as a passive incubator where the first organisms randomly encountered
54 tal manipulation outside of the microfluidic-incubator, where assembly can be done just before the st
55 uclear cells (PBMCs) cultured in typical CO2 incubators, which are equilibrated with air (21% O2).
56 tic resonance (MR) imaging, an MR-compatible incubator with air, temperature, and humidity regulators
58 es, control of osmolarity and pH outside the incubator with Hibernate and density gradient separation
59 ons cultured for 7-10 days were placed in an incubator with levels set at 0.1%, 1%, and 3% O2 and wer
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