Microscopic slides

Illustrated Instructions For Using CultureWell TM MultiSlip Coverslip Inserts

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Illustrated Instructions For Using CultureWell MultiWell Cell Culture System

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109093 AFB-Fluor - Staining kit for fluorescence-microscopic detection of acid-fast bacteria

the analysis of stained slides with a microscopic magnification >40x. Staining of histological samples Staining in the staining cell Deparaffinize histological slides in the conventional manner

Crystal Mount Aqueous Mounting Medium (C0612)

to 60 to 70 °C for 20 minutes. 4. Remove the slides from the oven and allow them to reach room temperature. The slides are now ready for microscopic visualization. Notes: • Do not

Millicell-24 Cell Culture Plate: Fixation and Immunostaining Guidelines

Visualizing Membranes on Microscope Slides (for higher magnification or with objectives with short working distances) The membrane can be removed from each well for microscopic evaluation. This allows

124653 4',6-Diamidino-2-phenylindole dihydrochloride (DAPI) for microscopy

15 min allow to run off thoroughly, dabbing the slide dry if necessary mount the slides with e.g. Aquatex® and cover glass microscope under UV excitation Microscopy 4’,6-Diamidino-2-phenylindole

FAQ: Millicell μ-MigrationAssay Kit (MMA205)

pre-stained before loading into the slide. 3. Can I use a normal digital camera connected to a microscope to take images manually at different time points (e.g. if the microscope doesn’t have video equipment

100361 ISOSLIDE® Reticulin Control Slides with reference tissue for the detection of reticular fibres in histology

is applied onto the slide next to the white printed labelling field. One slide is already stained with the reference method and is used for comparison. The 24 unstained slides are stained according

CLARION MOUNTING MEDIUM

to 80 °C for 15 to 30 min. Remove the slides from the oven and allow them to cool to room temperature. The slides are now ready for microscopic visualization. Notes: • Some tissue

User Guide

recover in the dark for 2 hours. Store slides in 4 °C. 6b. Microscope Observation Observe under microscope. If the cells on slide appear too dense/far apart, repeat the steps with higher/lower dilution

115930 Toluidine blue O (C.I.52040) for microscopy Certistain®

of stained slides with a microscopic magnification >40x. Result Nuclei dark blue Tissue blue Procedure - Metachromasia Staining in the staining cell Deparaffinize histological slides in the conventional

1.09204. Giemsa IFU

can then be stored. The use of immersion oil is recommended for the analysis of stained slides with a microscopic magnification >40x. Result Buffer solution Buffer solution Buffer solution pH 6.4

101287 Löffler's methylene blue solution - for microscopy

for the analysis of stained slides with a microscopic magnification >40x. Staining of histological samples Staining in the staining cell Deparaffinize histological slides in the conventional manner

Product Information Sheet -MBD0059

recover in the dark for 2 hours. Store slides in 4 °C. 6b. Microscope Observation Observe under microscope. If the cells on slide appear too dense/far apart, repeat the steps with higher/lower dilution

100380 ISOSLIDE® Iron Control Slides with reference tissue for the detection of free iron in histological tissue

analysis of stained slides with a microscopic magnification >40x. Result Free iron (Fe3+) intensive blue granules Nuclei pale red Cytoplasm tender pink Technical notes The microscope used should meet

MOUSE ANTI-HUMAN GOLGI ZONE MONOCLONAL ANTIBODY

concentration of 5 x 10 cells/mL in PBS are pipetted dropwise on PTFE- coated printed microscope slides containing ten 5 mM wells/slide. After the cells are allowed to settle to the surface of the glass (10-15

Data Sheet - CYTO4

clean, glass microscope slides and allow to dry at room temperature (25 °C) for 5-16 hours. 6. Immerse the slides in the pre-cooled acetone (−20 °C) for 20 minutes. 7. Allow slides to dry briefly

102472 ISOSLIDE® Warthin-Starry Control Slides with reference tissue for the detection of Helicobacter pylori and Spirochetes in histological tissue

tissue is applied onto the slide next to the white printed labelling field. One slide is already stained with the reference method and is used for comparison.The 24 unstained slides are stained according

Data Sheet - CYTO1

clean, glass microscope slides and allow to dry at room temperature (25 °C) for 5-16 hours. 6. Immerse the slides in the pre-cooled acetone (−20 °C) for 20 minutes. 7. Allow slides to dry briefly

MOUSE ANTI-HUMAN NUCLEOLI MONOCLONAL ANTIBODY

concentration of 5 x 106 cells/mL in PBS are pipetted dropwise on PTFE- coated printed microscope slides containing ten 5 mm wells/slide. After the cells are allowed to settle to the surface of the glass (10-15 minutes

101979 DPX - water-free mounting medium for microscopy

in a fume hood. The slides are mounted by dropping approx. 0.2 ml of the listed mounting me- dium onto the horizontal slide using a glass rod, which will fi ll the space between slide and cover glass. As

108635 Kaiser's glycerol gelatine, phenol-free - for micorscopy

analysis of stained slides with a microscopic magnification >40x. Result The use of these aqueous, ready-to-use mounting media results in com- pletely airtight specimen slides, the structure and stain

115948 Safranine O (C.I. 50240) for microscopy Certistain®

just a few hours. The use of immersion oil is recommended for the analysis of stained slides with a microscopic magnification >40x. Result Gram-positive microorganisms blue-violet Gram-negative

FETAL HEMOGLOBIN

labeled microscope slides, make thin blood smears. Pre pare CONTROL slides using positive HbF blood (cord-blood) and normal adult blood. Air dry approximately 10 minutes. 3. Fix slides by immersing

Data Sheet - 77730

remove the excess water. Alternatively, the slide may shaken to remove most of the water and air-dried. 9. Examine the finished slide under a microscope (oil immersion objective). Attention: Wash

MOUSE ANTI-HUMAN NUCLEAR SPLICEOSOMES MONOCLONAL ANTIBODY - Data Sheet

concentration of 5 x 106 cells/mL in PBS are pipetted dropwise on PTFE- coated printed microscope slides containing ten 5 mm wells/slide. After the cells are allowed to settle to the surface of the glass (10-15

115933 Certistain® Carmine (C.I. 75470) (calcium-aluminium lacquer of carminic acid) for microscopy Certistain®

for the analysis of stained slides with a microscopic magnification >40x. Result Glycogen red Mucous, fibrin, amyloid pink to red Technical notes The microscope used should meet the requirements

115937 Fuchsin (C.I. 42510) for microscopy Certistain®

for just a few hours. The use of immersion oil is recommended for the analysis of stained slides with a microscopic magnification >40x. Result Acid-fast bacteria (AFB) red Background light blue

104095 Glycerol for fluorescence microscopy

analysis of stained slides with a microscopic magnification >40x. Result The use of these aqueous, ready-to-use mounting media results in com- pletely airtight specimen slides, the structure and stain