Routine Transmission Electron Microscopy (TEM) Staining Protocol for Cultured Cells

 

 

 

Fixation:

  1. Fix cell suspension or free cells in 4% formaldehyde and 1% glutaraldehyde in 0.1 M PB (pH 7.4) by mixing equal volume of fixative and cell suspension.

  2. Transfer cells to centrifuge tube and spin for 10 minutes. A nice, tight pellet will be formed (Re-spin if necessary during processing). Carefully pipette off fixative. Add fresh fixative for at least 2 hours or overnight.
  3. Pipette off fixative. Replace with 8% (0.2M) sucrose in 0.1 M PB 3x15 minutes or overnight at 4 C (Samples can be kept in sucrose for a long time).
  4. Post-fix with 1% OsO4 in 0.1 M PB for 1 hour.
  5. Pipette off OsO4, Rinse in 0.1 M PB 3x10 minutes.

Dehydration:

  1. 50% ethanol  15min

  2. 70% Ethanol  15min

  3. 95% Ethanol  15min

  4. 100% Ethanol  2x15min
  5. 100% Propylene oxide  2x15min
  6. 1:1 EMBed 812 and Propylene Oxide for1-2 hour.
  7. 2:1 EMBed 812:Propylene Oxide overnight in dessicator with top off.

Embedding:

Embed in Beam capsules, and bake in 60 ºC oven for 48 hours.

 

Sectioning:

Semithin (thick section, 0.5-1 um) and toluidine blue staining. Observe the thick section, and trim EM block further if needed. Then ultrathin sectioning, and collected on grids.

 

Staining:

 

Staining grids with uranyl acetate (see reagent below) for 15 minutes, rinse with distilled water and then staining with lead citrate (see reagent below) for 3-5 minutes, rinse with distilled water.

 

Solutions and Reagents:

 

0.2M PB, pH 7.4:

Na2HPO4 ------------------------ 21.8 g

NaH2PO4 ------------------------ 6.4 g

Distilled water ----------------- 1000 ml

 

4F1G Fixative (4% Formaldehyde & 1% Glutaraldehyde in 0.1 M PB, pH 7.4):

0.1M PB, pH 7.4 --------------- 88 ml

37-40% Formaldehyde ----- 10 ml

50% Glutaraldehyde --------- 2 ml  

 

8% (0.2M) Sucrose in 0.1M PB:

Sucrose ------------------------- 8 g

0.1 M PB ------------------------ 100 ml

 

1% Osmium in 0.1M PB:

2% Osmium -------------------- 5 ml

0.2M PB, pH7.4 --------------- 5 ml

 

5% Uranyl Acetate Solution:

To prepare 50 ml, add 2.5 g of uranyl acetate to 50 ml of distilled water. Cover with foil and stir overnight. Add 10 drops of glacial acetic acid. Store solution in 4 ºC.

 

Reynold’s Lead Citrate Solution:

To prepare 50 ml, add chemicals in distilled water in following order

Lead nitrate ------------------------------ 1.33 g

Sodium citrate, dihydrate -------------- 1.76 g (solution becomes cloudy when sodium citrate is added)

1N NaOH ----------------------------------- 5 ml  (solution becomes clear when NaOH is added)

Distilled water ----------------------------- 30 ml

Stir for 10 minutes to dissolve and add additional 15 ml of distilled water. Store solution for 3-6 months at 4 ºC. Note: the mount of NaOH is very important. Too much will make solution cloudy.

 

EMBed 812:

 

Final Volume

EMBed-812

DDSA

NMA

DMP-30 (2%)

20.91 ml

10 ml

4.5 ml

6 ml

0.41 ml

31.37 ml

15 ml

6.75 ml

9 ml

0.62 ml

41.82 ml

20 ml

9 ml

12 ml

0.82 ml

52.28 ml

25 ml

11.25 ml

15 ml

1.03 ml

        Mix all four components in plastic beaker and stir with wood stick.