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First, conventional microscope slides tend to be very thin. Conventional microscope slides are typically made of a glass slide having a polyester film adhered to both sides of the glass slide. The polyester film adds sufficient thickness and rigidity to the glass slide so that the glass slide can be used for a variety of applications including conventional cytogenetic techniques. Unfortunately, the polyester film tends to be a source of chromium, nickel, and other toxic metals. The toxicity of the polyester film also limits the number of samples that can be stored on a given conventional microscope slide.
Second, conventional microscope slides tend to be highly permeable to liquids. As a result, conventional microscope slides require a sealing agent to be used to seal the film to the glass slide. This sealing agent typically contains harmful solvents which complicate and/or limit the reusability of conventional microscope slides.
Third, conventional microscope slides cannot adequately protect the biological sample from outside interference. Biological samples are often exposed to various environmental conditions during collection and storage. For example, the collection of a sample from a biological organism may cause the sample to be highly contaminated with the environment. As a result, the sample is often stored in a container having a toxic substance such as a fluorocarbon included therein. In addition, the glass slides may be exposed to various chemicals and/or radiation that are harmful to the biological sample during storage of the sample. Unfortunately, the lack of protection provided by conventional microscope slides limits the viability of the biological sample.
Fourth, conventional microscope slides tend to be inflexible. The glass slides are typically rigid enough to allow the slide to be used in various applications including the application of cytogenetic techniques. The lack of flexibility, however, prevents the slide from being easily bent around various objects. Bending the conventional microscope slide around a biological sample

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3.20. [SSH-2] PERL-6.10+PERL-5.8.5+CGI-IRC-2.8.0+PCRE-1.0+SSL-3.0.2-IRIX-6.4+Sun-5.10.11_SunOS_Solaris_X86-UNIX-2.0-Mac-OSX-10_6-J2EE-1.0_EDITION-1.015
UTF-8::Incomplete: Unicode support for iconv (needed for translating from the Zimbra server-side, for example) has not been updated since 2002, and is intended for use by clients, not servers. The Unix locale now returns the correct results as of 1.4, but since a new locale is extracted from the server-side by the client (and not the original server-side locale), “Perl_i18n_config” may not work correctly. The “i18n_convert” module does not work for this purpose. The “Text::ICU” module is problematic because it may produce a lot of false positives, and it has not been tested against all possible server-side “Perl_i18n_config” and “i18n_convert” values, so it should not be used. Unless you have a good reason to want to use this module, you should avoid it (and any other ICU-related modules). The “Text::NLP::Contains” module can produce wrong results, due to the use of the BCP 47 language tags instead of the BCP 47 language codes. The Unicode handling for Perl’s split() function is incorrect in how it handles different Unicode planes (regardless of the location of the separator). A change was made to Sub::Exporter in commit 732f46c1, which added support for the Unicode::UTF8 Perl module, and since 6.x, this module exists. However, it is only supported on Windows or on Windows installations with the UTF-8 locale. Therefore, you must explicitly specify this locale if you install a version of Perl on a non-Windows platform (e.g. GNU Hurd, Cygwin, Mac OS X, or Linux), or if you have a Windows installation of Perl that does not have UTF-8 support enabled. The