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Oil Red O Staining Protocol

This document provides instructions for performing an Oil Red O staining assay to detect mature adipocytes in cultured cells undergoing adipogenesis. Key steps include: 1) Fixing the cell cultures in 10% formalin for 30-60 minutes. 2) Preparing an Oil Red O working solution by mixing Oil Red O stock solution with water and filtering. 3) Staining the fixed cell cultures with Oil Red O working solution for 5 minutes to stain lipids red, then hematoxylin to stain nuclei blue. 4) Rinsing the stained cultures with water and viewing under a microscope, where mature adipocytes will appear red due to lipid accumulation.

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948 views2 pages

Oil Red O Staining Protocol

This document provides instructions for performing an Oil Red O staining assay to detect mature adipocytes in cultured cells undergoing adipogenesis. Key steps include: 1) Fixing the cell cultures in 10% formalin for 30-60 minutes. 2) Preparing an Oil Red O working solution by mixing Oil Red O stock solution with water and filtering. 3) Staining the fixed cell cultures with Oil Red O working solution for 5 minutes to stain lipids red, then hematoxylin to stain nuclei blue. 4) Rinsing the stained cultures with water and viewing under a microscope, where mature adipocytes will appear red due to lipid accumulation.

Uploaded by

Anonymous GpgioaDAb
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Lampiran 8

Oil Red O Staining of Cultures Being Tested for Adipogenesis

Background
Oil Red O staining is an assay performed to stain induced adipogenic cultures to detect mature
adipocytes.

Required Materials
Cells being tested for adipogenesis
PBS (without Ca++ or Mg++)
10% Formalin solution, neutral buffered (Fisher SF98) available in each fume hood to be
used
Oil Red O (Fisher M312512)
99% Isopropyl Alcohol
DI water
60% Isopropyl Alcohol
Hematoxylin (Fisher SH30-500D)
Whatman conical filter paper (Fisher 09-845); 4 funnels; 4 50 ml tubes, each in its own rack
set out near the instructors lecture bench
Tap water
Formalin waste container in each fume hood to be used
Coplin jars for rinsing 10, all filled with tap water
P1000 micropipettor and tips (barrier tips are not necessary)

General Considerations
All procedures involving formalin must be done in a fume hood. Take care not to leave the cells dry
for more than 30 seconds throughout this assay. Gently add and remove all reagents indirectly to
the monolayer to avoid cell detachment. For example, drip the reagent down the side of the culture
well.

Fixing Adipogenic Cultures


1 Remove cultures from incubator and place in a fume hood. Remember, the fume hood
exhausts noxious fumes. The biosafety cabinets do NOT exhaust fumes.
2 Using your micropipettor, gently remove media from the wells, always from the controls first.
3 Gently rinse each well twice with 1.0 ml PBS.
4 Remove all the PBS and add 1.0 ml 10% formalin. Incubate 30-60 minutes at room
temperature (RT).

Preparing Oil Red O Stain


1 Prepare a stock solution by weighing out 300mg of Oil Red O powder and adding this to
100 ml of 99% isopropanol. This stock solution is stable one year from the date it was
made. (This step will be performed by our Instructional Support Technician.)
2 During the last 15 minutes of your formalin fixation, In the fume hood, mix 15 mls Oil Red O
stock solution with10 mls DI water in a 50 ml tube.
3 Incubate 10 minutes at room temperature. This working solution is stable for only 2 hours.
4 Place a piece of Whatman filter paper in a funnel above a second 50 ml tube. Filter the Oil
Red O working solution completely through the filter funnel into the second 50 ml tube.
Move as soon as possible to the next section of the protocol.

Staining Adipogenic Cultures this procedure must be done as quickly as possible to


avoid thickening of the Oil Red O
1 Remove the formalin from each well and discard it according to your chemical waste
disposal procedure.
2 Gently rinse each well twice with 1.0 ml DI water. Remove and discard as formalin waste.
3 Add 1.5 ml 60% isopropanol to each well and let sit for 5 minutes.
4 Remove isopropanol and add 1.5 ml Oil Red O working solution to each well, be sure to
cover the entire monolayer. Incubate 5 minutes at room temperature.
5 Remove Oil Red O and rinse cultures with changes of 1.5 ml RT tap water until the water
rinses off clear.
6 Add 1.5 ml hematoxylin stain into each well, be sure to cover the monolayer. Incubate 1 min
at RT.
7. Remove the hematoxylin and remove the chamber [Link] rinse the cultures with room
temp tap water in successive coplin jars until the water rinses off clear.
8. Place a coverslip over the cells with water. View on a phase contrast microscope. Lipids
appear red and nuclei appear blue.

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