3. Tissue array using Quick-Ray™
IMPORTANT NOTES
• Explanation of Symbols used
WARNING: WARNING indicates an injury hazard not immediately accessible
as you read this symbol. It calls attention to an operating procedure, practice,
or like that, if no correctly performed or adhered to, could result in personal
injury or death. Do not proceed beyond a WARNING notice until the
indicated conditions are fully understood and met.
BIOHAZARD WARNING: BIOHAZARD WARNING indicates an injury hazard
not immediately accessible as you read this symbol.
Biohazard(Infectious agent): A type of micro-organism, bacteria, mold parasite
or virus which normally causes, or significantly contributes to the cause of,
increased morbidity or mortality of human beings.
• SAFETY NOTES
Read the following safety notes to avoid injury and prevent damage to this
product or any products connected to it.
To avoid personal injury
• Be careful not to pinch your fingers when closing the wooden case.
• Keep the Quick-RayTM and accessories out of the reach of small children.
• Be careful for your fingers or hand not to be scratched by the needle of tip
when assembling or disassembling the tip or the probe, or when cleaning the
tip.
Use the Quick-RayTM and accessories according to the instructions in this manual
• Use the Quick-RayTM and accessories according to the instructions in this
manual. No authorization for the analysis or modification of the Quick-RayTM is
provided.
• Do not use accessories that are not supplied or recommended by UNITMA.
• Contact UNITMA for repairing or service or buying accessories.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
4. Tissue array using Quick-Ray™
Do not use the donor block or a sample with a biological hazard or a chemical hazard.
• Do not use the donor block or a sample with a biological hazard or a chemical
hazard that can impact human health.
Handle biohazards.
• Working with infectious material requires the following precautions.
a. Limit access to areas where experiments with infectionus specimens are in
progress.
b. Clearly label areas where biohazards are in use and designate specific
areas where biohazards are routinely used, using this symbol (black on red
background):
c. Wear lab coat, gloves and safety glasses to prevent contamination from the
infectious specimen, and remove them when leaving the work area.
d. Decontaminate work surfaces once per day and after any spill of viable
specimen.
e. Eating, drinking and applying cosmetics are not permitted in the work area.
f. Wash hands after handling viable specimens before leaving the lab.
g. Transport contaminated materials in a red biohazard bag which has been
placed in a labeled, leak-proof container.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
5. Tissue array using Quick-Ray™
Biohazard Determination.
• Lab Biosafety Level Criteria.
The following guidelines can be used by all laboratory personel.
a. Biosafety Level 1 is appropriate for undergraduate and secondary
educational training and teaching laboratories and/or other facilities in which
work is done with defined and characterized strains of viable microorganisms
not known to cause disease in healthy adult humans.
b. Biosafety Level 2 is applicable to clinical, diagnostic, teaching and other
facilities in which work is done with the broad spectrum of indigenous
moderate-risk agents present in the community and associated with human
disease of varying severity.
c. Biosafety Level 3 is applicable to clinical, diagnostic, teaching, research, or
production facilities in which work is done with indigenous or exotic agents
where the potential for infection by aerosols is real and the disease may have
serious or lethal consequences.
d. Biosafety Level 4 is applicable to work with dangerous and exotic agents
which pose a high individual risk of life-threatening disease.
• Practices and Techniques, Safety Equipment
Biosafety Practices and
Safety Equipment Facilites
Level Techniques
None: primary containment
Standard provided by adherence to
1 microbilogical standard laboratory Basic
practices practices during open bench
operations.
Level 1 practices plus: Partial containment
Laboratory coats; equipment (i.e., Class I or II
decontamination of all Biological Safety Cabinets)
infectious wastes; used to conduct mechanical
2 limited access; manipulative procedures Basic
protective gloves and that have high aerosol
biohazard warning potential that may increase
signs the risk of exposure to
as indicated. personnel.
Level 2 practices plus: Partial containment
special laboratory equipment used for all
3 Containment
clothing; controlled manipulations of infectious
access. material.
No facilities available Maximum
Maximum containment
4 on this campus at this Containment
equipment.
time.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
6. Tissue array using Quick-Ray™
Tissue Microarray ?
"Tissue Microarray (TMA)" is the technology to attach the individual tissue cores in one slide.
The TMA consists of cylindrical paraffin embedded tissues (cores) that are acquired from donor
blocks. "The donor block" is a standard tissue block from surgical pathology, autopsy or research
material. Donor blocks are marked on both slides and tissue blocks to identify morphologically
representative areas of interest. The tissue cores are extracted from the donor block and
inserted into a recipient block. Tissues can be inserted with up to 1000 tissue cores in a recipient
block by using a precise instrument or tool. Thin cross-sections cut from the recipient block (TMA
block) with a microtome are placed onto standard slides for in situ analysis. One TMA block can
generate between 100 and 500 sections.
These TMA technology can attach tissues of several patients or animals on only one slide, and
compare analysis on several genes and protein expression of same tissue, and execute analysis
under same condition. So, it reduces reagent and time, and expenses to 1/60, and increases
research effectiveness. TMA is used widely in recent pathological research analyses, and it is
applicable to most methods used as tissues like Immunohistochemistry, in situ hybridization,
FISH, in situ PCR and so on Tissue.
But the manufacturing of TMA is a critical step in the success of the technology. This creates
tremendous obstacles and impediments for the pathologists to fully utilize the power of TMAs.
Quick-Ray™, the Patented Technologies of UNITMA, overcame these road blocks and
decreased the current time to create Block and Slide in innovative way by providing solutions to
empower the pathologist to easily set up their TMAs with ready-to-go and pre-formed recipient
blocks.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
7. Tissue array using Quick-Ray™
Quick-Ray™ SYSTEM
• Minimized size arrayer comparing with the conventional products
• Portable, easy to carry and to make the array block anytime and anywhere
• Easy to handle. Inexperienced pathologist can handle easily in the lab.
• Simple developing procedure
• Easy to create the various sized block with using disposable bases
• Steel array block and cassette array block are available
• Low cost to purchase
TISSUE MICROARRAY SET
Quick-RayTM • Quick-Ray™
Weight : 140g
Length : 15.5Cm
• Tip & Recipient block
Tip core size
∅ 1mm
∅ 2mm
∅ 3mm
Base Mold ∅ 5mm
Recipient block
• Guide for 1mm recipient block
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
8. Tissue array using Quick-Ray™
CONSUMABLES
• Disposable-base (Recipient block) • Cassette & Base mold
∅ 5mm x 20 well
∅ 3mm x 30 well
∅ 2mm x 60 well
∅ 1mm x 120well
APPLICATION
• Special stain
• Immunohistochemistry
• in situ hybridization
• FISH
• in situ PCR etc.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
9. Tissue array using Quick-Ray™
PROCEDURE
• How to build
1. Place the reference slide and the donor block on
microscope stage for position marking with an oil pen.
2. Extract the marked tissue from the donor block by using the Quick-Ray™ needle.
1) Place the donor block on a horizontal and flat table.
2) Hold the Quick-Ray™ in your hand and tighten your grip.
3) Hold the Quick-Ray™needle perpendicular to the marked
position of the donor block.
4) Insert the Quick-Ray™ needle into the donor block at the
proper depth of 5mm slowly.
(Don’t insert it quickly and too deep to prevent to damage
the donor block and the Quick-Ray™ needle.)
* Quick- Ray™ needle’s depth: 5mm
* Incubate the easily breaking donor block in a heating oven or a chamber at 37~40℃ for 15
~ 20 minutes.
3. Deliver the extracted tissue into the corresponding holes of the recipient block that were pre-
made by UNITMA, with Quick-Ray™ needle.
1) Place the recipient block on a horizontal and flat table.
2) Hold the Quick-Ray™ needle with the extracted tissue
perpendicular to the corresponding holes of the recipient
block.
3) Inject the extracted tissue (core) into the corresponding
holes of the recipient block at the proper depth of 4mm by
pushing the Quick-Ray™ plunger slowly.
4) Adjust the height of all the core with a same settings by
pressing the top of all the core with a flat side of a thing.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
10. Tissue array using Quick-Ray™
4. Put the recipient block into embedding mold with
cutting section faced down and incubate it in oven
at about 70℃ for 30~60 minutes.
(The top side of the recipient block in ‘Step 3’ will
be cutting section.)
5. Take out the recipient block when completely transparent. ⇒ Embedding
Step 1 for Embedding Step 2 for Embedding Step3 for Embedding
6. Solidify the block in cold plate.
7. Cutting (about 4㎛)
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
11. Tissue array using Quick-Ray™
• How to use the guide
1. Put the recipient block into the prop hole at bottom side.
2. Fit the 1mm guide on the prop.
3. Extract the marked tissue from the donor block by using Quick-Ray™ needle.
4. With fixing the prop by hand, insert the Quick-Ray™ needle into the guide hole, and put the
extracted tissue into the recipient block hole by pushing the knob down.
5. Remove the guide and recipient block from the prop.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
12. Tissue array using Quick-Ray™
6. Put the recipient block into embedding mold with cutting section faced down and incubate it in oven
at 60˚C for 30 minutes
7. Take out the recipient block when completely transparent
⇒ Embedding
8. Solidify the block in cold plate
9. Cutting
* In case of using 2, 3 and 5mm recipient block, insert the extracted tissue directly into the recipient
block without the guide by pushing the Quick-Ray™ knob down.
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
13. Tissue array using Quick-Ray™
BLOCK & SLIDE
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com
14. Tissue array using Quick-Ray™
ORDER
Unitma Co., Ltd., 3F Chungmyeong B/D, 224-8, Jamsil-Dong, Songpa-Ku, Seoul, 138-220, Korea
TEL 82-2-420-0070. FAX 82-2-420-9797
E-mail unitma@unitma.com http://www.unitma.com