LacZ staining of cells

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# add staining solution
# add staining solution
# incubate over night at 37°C
# incubate over night at 37°C
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== sample stains ==
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<gallery>
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Image:XGal_weak_ESC_200x.jpg|weak LacZ stain from modified mouse embryonic stem cells, 200x
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Image:XGal_strong_ESC_100x.jpg|strong LacZ stain from modified mouse embryonic stem cells, 100x
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</gallery>
== see also ==
== see also ==

Revision as of 11:43, 26 February 2007

Contents

material

  • X-Gal stock is 200 mg/ml in dimethylformamide (DMF)
  • K ferri-cyanide ( 50mM )=K3 is 0,33 g / 20 ml PBS ( Sigma Cat.# P-8131)
  • K ferro-cyanide ( 50mM )=K4 is 0,42 g / 20 ml PBS ( Sigma Cat.# P-9387)

staining solution

  • make fresh
  • heat mix to 50°C before adding X-Gal, in order to avoid precipitation
10 ml15 ml30 ml50 ml
X-gal ( 200 mg/ml)50 µl75 µl150 µl250 µl
MgCl2 (1M)20 µl30 µl60 µl100 µl
K ferri-cyanide ( 50mM )=K31 ml1,5 ml3 ml5 ml
K ferro-cyanide ( 50mM )=K41 ml1,5 ml3 ml5 ml
PBS ( up to...)7,9 ml8,5 ml23,5 ml39,6 ml

fixation solution

  • make fresh
10 ml15 ml30 ml50 ml
formaldehyde/methanal ( 37 %)541 µl811,5 µl1,62 ml2,7 ml
glutaraldehyde ( 25 %)40 µl60 µl120 µl200 µl
PBS (up to...)9,42 ml14,13 ml28,26 ml47,1 ml

common mistakes / tips

  • time of fixation is crucial; overfixing cells will reduce LacZ activity
  • some cell types are easy to detach by squirting liquid onto the dish; be careful;
  • X-Gal will precipitate if solution cools too much

steps

  1. carefully wash cells once with PBS (avoid detaching cells by strong pipetting)
(volume is around 5 ml for 10 cm-dish
                  3 ml for 6 cm-dish			
                 500µl for a 24 well)		
  1. add fixative solution
  2. incubate 2 min (Time is important !)
  3. carefully wash 3 times with PBS (1st wash must be quick to avoid overfixation in the last samples to be washed)
  4. add staining solution
  5. incubate over night at 37°C

sample stains

see also

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