油紅O溶液 | Oil Red O Solution中性脂質染色劑 Servicebio貨號G1015-100ML  (6:4 以ddH2O混合 60-70 ℃ 加熱後使用)

產品介紹:

油紅O又稱蘇丹紅5B(Sudan red 5B),是一種脂溶性偶氮染料(fat soluble azo dye)。這種染料可以特異性地染色細胞(cells)或組織(tissues)中的甘油三酯等中性脂質(neutral lipids),但對磷脂(phospholipids)和類固醇(steroids)的染色較弱。基本原理是油紅O(oil red O)溶於脂類(lipids),使脂類(lipids)呈紅色至橙紅色(orange red)。

本品飽和油紅O染料溶液(saturated oil red O dye solution)為油紅O飽和溶液(oil red O),臨用前用蒸餾水稀釋後用於組織切片(tissue sections)或細胞染色。染色後,組織中的脂肪滴(fat drops)呈紅色(red)至橙紅色。 可搭配脂肪專用固定溶劑使用 脂肪專用固定液試劑盒 | Special Fixative Solution for Fat Servicebio貨號G1119-250ML

 

Oil red O, also known as Sudan red 5B, is a fat soluble azo dye. This dye can specifically stain neutral lipids such as triglycerides in cells or tissues, but it is weak for phospholipids and steroids. The basic principle is that oil red O dissolves in lipids to make lipids red to orange red.

The saturated oil red O dye solution of this product is the saturated solution of oil red O. It can be used to dye tissue sections or cells after being diluted with distilled water before use. After dyeing, the fat drops in the tissues are red to orange red.

Assay Protocol 

l Preparation of working solution: before use, (6:4) six portions of saturated oil red O dye solution and four portions of distilled water shall be fully mixed, placed in a 60-70 ℃ water bath for 30 minutes, and then filtered with qualitative filter paper after natural cooling to obtain oil red O working solution. It needs to be prepared and used now. In addition, 60% isopropanol is required.

l Sample preparation

  1. For cells: aspirate the cell culture medium, slowly add PBS (G4202 is recommended) to the edge of the orifice plate to simply clean the cells. Add 4% paraformaldehyde fixative (G1101 is recommended) and fix it at room temperature for 8-10 min, and rinse it twice with PBS.
  2. For frozen sections: take out the sections from - 20 ℃ and let them stand at room temperature for 5-10 min to recover to normal temperature.

l Dyeing steps

  1. For cells

(1) Add a small amount of 60% isopropyl alcohol into the pore plate to cover the cells for 15-20 seconds, and then suck out 60% isopropyl alcohol and dry the water slightly.

(2) Add oil red O working solution to the orifice plate to cover the cells, and dye them at room temperature in dark for 30 min to remove the dye.

(3) Add 60% isopropanol for rapid differentiation for 3-5 seconds, wash with pure water for 3 times, and each time for 5 minutes.

(4) (Optional) Add hematoxylin dye solution (G1004 is recommended) to dye the nucleus, wash with water, turn blue and then wash with water.

(5) PBS was added to cover the cells and observed under microscope. In case of cell climbing, glycerol gelatin film sealant (G1402 is recommended) can be used for slide mounting.

  1. For frozen sections

(1) Frozen sections recovered to room temperature were gently immersed in oil Red O working solution and stained for 8-10 min (covered to avoid light).

(2) The sections were taken out, stayed for 3 s, and then immersed in two cylinders of 60% isopropanol for differentiation for 3-5 s.

(3) Sections were immersed in two cylinders of pure water for 10 s each time.

(4) (Optional) The sections were immersed in hematoxylin dye solution to stain the nuclei, washed with water, then returned to blue and washed again. After slightly drying, glycerin gelatin was added to mount the slide.

Note:

  1. If it is a frozen section of fresh tissue, the section should be fixed before staining.
  2. Oil Red O working fluid must be prepared and used at present. The heating process must be sealed to prevent solvent volatilization.
  3. During the whole operation, pay attention to the gentle action to avoid fat loss or displacement.
  4. Samples stained with oil Red O cannot be stored for a long time, and should be observed and photographed as soon as possible.
  5. When using glycerin gelatin to mountslides, attention should be paid to avoid bubbles as far as possible. If bubbles are not allowed to press the glass slide or forcibly tear the cover glass after mounting the slides, it will cause fat displacement. The slide can be immersed in warm water at 50-60 °C to allow the cover slide to fall off and then re-mount the slide.
  6. For your safety and health, please wear a lab coat and disposable gloves during operation.

Servicebio台灣品牌介紹-BRAND/AGENCY/品牌介紹- Servicebio

【Servicebio品牌】

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