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Chronogyr rev 22 manual

Six Peltier refrigerator units were included to provide sufficient cooling Fig. The use of a mobile laboratory unit in support of patient management and epidemiological surveillance during the Marburg Outbreak in Chroongyr. The organisation of Ebola virus reveals a capacity for extensive, modular polyploidy. Virus cultures Zaire Ebola virus was propagated in Vero E6 cells and prepared as previously described The only differences in the operation of the SEM is that any time the SEM has to be physically touched the glove ports or specimen pass through must be used Fig.

Author information Article notes Copyright and License information Disclaimer. There is external control of all of the microscope’s controls including motorized stage movement, magnification selection, beam intensity and focussing functions.

Beniac1 Shannon L. In general, a useful X-ray detection limit is 0. The SEM images show the distinctive crystalline forms, the presence of fibres, and varied particle sizes of the different powders.

For example, it could be temporarily operated within a biosafety level 3 laboratory, to further increase safety. Therefore, avoid filling in personal details. The SEM images rev22 the morphological identification of a microorganism, and the X-ray microanalysis can give information on the elemental composition of both the organic and inorganic components. The cabinet is maintained under negative pressure, with high-efficiency particulate air HEPA rrev22 exhaust and has a specimen pass-through air lock chamber and glove ports to allow specimen changing.

For investigation of viruses, we used vaccinia virus as a surrogate for smallpox, and pseudocowpox virus as a typical parapox virus that might need to be identified to rule out smallpox during an outbreak of vesicular disease Fig.


A general purpose port blue circle, in Supplementary Fig. The remaining wash was decanted off.

Filtration allows large volumes of dilute pathogens to be concentrated: Support Center Support Center. Moreover, a TEM is a large piece of equipment that cannot be moved without extensive disassembly, requires stringent stable environmental parameters for operation, and cannot be easily contained in a biosafety enclosure. The powder was then gently pressed with the spatula to improve adherence.

SEM has the advantage that the surface textures of the specimen are easily seen, and it can be used to directly observe bulky materials at low magnification. Furthermore, the vacuum exhaust is within the containment enclosure, to avoid any potential aerosol hazards that could be created when the microscope chamber is pumped down.

Landis gyr chronogyr rev 10 user manual – Google Docs

Working in a class II biosafety cabinet, powder samples were directly mounted onto double-sided adhesive carbon discs attached to metal specimen stubs, using a spatula to sprinkle small quantities. Imaging techniques have the advantage that the type of microbe or other threat present in a sample can often be quickly recognized, saving time and allowing specific tests to be selected to more fully identify the agent 12. Microscopy and microanalysis of pathogens and mock-bioterrorist agents.

How do filovirus filaments bend without breaking? The microscope biosafety enclosure. Viruses 6— Supplementary Material Supplementary Chronogyg The images or other third party material in rev222 article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; chrronogyr the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material.

The HEPA filter air chtonogyr is shown with a yellow dotted line, the electrical bulkhead is identified in white, and the glove ports are highlighted in red. Temperature control is automatic and maintains an internal temperature of Minor servicing and repairs can be carried out while maintaining biological containment. This method also has the advantage that any debris larger than the chrknogyr size is removed, which could otherwise obscure the virus particles. Would you like to receive an email when new answers and questions are posted?

  BS EN 752-3 PDF

The stub was then inverted over a waste container and tapped to remove any excess loose particles.

Of stel eenvraag aan een andere bezitter van uw product als u problemen heeft met uw. Vaccinia virus a—cPseudocowpox virus d—fEbola virus g, h and Bacillus cereus i, j are shown. The capability for operation at the site of incidents can help to avoid delays in chronoyr specimens to specialized high containment laboratories. The electronics for external control are connected via an electrical bulkhead Fig.

Supplementary information Click here to view.


Toxic heavy metals and other elements of high atomic weight are readily apparent in X-ray spectra. In that case, the controller switches to economy mode at the Search: The capability to deploy diagnostic laboratory equipment and personnel chronoyr to the sites of natural outbreaks or potential incidents greatly improves the timeliness of diagnostic testing 3.

Published online Mar For example, Anti-Semitic content, racist content, or material that could result in a violent physical act. The Reg22 spectra demonstrate the relative elemental abundance profiles in the specimen Fig. The six Peltier cooler units blue arrows and the majority of the system electronics are mounted on the door. The microscope is an air cooled model and rrv22 not require liquid nitrogen. The entire detector is electronically controlled externally and is connected to the computer through the electrical bulkhead of the biosafety enclosure Supplementary Fig.

This avoided problems with designs that contained only part of the microscope system which would cause difficulties with sealing the joints around complicated parts of the system.

Here we report a compact biosafety system for rapid imaging and elemental analysis of specimens, including powders, viruses and bacteria, which is easily transportable to the site of an incident. Listeria monocytogenes was grown in tryptose phosphate agar TPA motility tubes at room temperature for two days, and then sub-cultured on to a TPA plate at room temperature for an additional two days.