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The Principles of Clinical Cytogenetics - Extra Materials - Springer

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Automation in the <strong>Cytogenetics</strong> Laboratory 117<br />

Fig. 4. Floor model drying chamber. (Courtesy <strong>of</strong> <strong>The</strong>rmotron Industries.)<br />

as heating), this chamber has been modified to control humidity as well, and fans have been installed<br />

to allow for control <strong>of</strong> airflow over the cover slips. <strong>The</strong> advantages to this type <strong>of</strong> hardware are its<br />

ability to maintain conditions, quick recovery time after opening the chamber to insert or remove<br />

dishes, and potential for external venting if necessary. <strong>The</strong> disadvantage is the necessity to remove<br />

the fixative prior to placing the dishes in the chamber, creating the potential for drying to begin under<br />

noncontrolled conditions if there is any delay in getting the dishes into the chamber.<br />

A variation on this theme is shown in Fig. 4. Here, the entire drying process, including aspiration<br />

<strong>of</strong> fixative, can take place inside the chamber. <strong>The</strong> technologist sits at the unit and manipulates the<br />

processing with a glove-box approach. <strong>The</strong> drawback to this concept is the large size <strong>of</strong> the unit, and<br />

a somewhat more cumbersome and limiting setup; removing one or more cultures for examination<br />

(an absolute requirement) can be more intrusive to the workflow.<br />

<strong>The</strong>se condition-controlled chambers are gaining in popularity in cytogenetics laboratories, and<br />

some use them not only for in situ processing but also for routine slide making because <strong>of</strong> the consistency<br />

they provide.<br />

INSTRUMENTATION FOR FISH<br />

Although FISH (see Chapter 17) represents one <strong>of</strong> the most exciting and clinically significant<br />

developments <strong>of</strong> the last decade, most <strong>of</strong> the steps involved in preparing samples for analysis are<br />

unremarkable and <strong>of</strong>ten repetitive and, therefore, lend themselves to automation. When one considers<br />

the enormous increase in FISH sample volume most cytogenetics laboratories are experiencing,<br />

any device that can reduce the labor component <strong>of</strong> the process becomes indispensable.

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