Griffin:Immunohistochemistry Paraffin

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'''Immunohistochemistry Protocol'''
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==Immunohistochemistry Protocol 1==
John M. Sanders B.S. Cardiovascular Research Center, University of Virginia Charlottesville, VA.
John M. Sanders B.S. Cardiovascular Research Center, University of Virginia Charlottesville, VA.
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'''15.''' Coverslip
'''15.''' Coverslip
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==Immunohistochemistry Protocol 2==
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'''1.''' Deparaffinize and rehydrate
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5 min tray
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2 x xylene
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2 x absolute ETOH
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2 x 95 % ETOH
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2 x 70 % ETOH
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2 x milliQ H2O
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'''2.''' [http://openwetware.org/wiki/Griffin:Antigen_Retrieval_Technique Antigen Retirieval]
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'''3.''' Rinse sections in 2 changes of PBS washing buffer in separate beakers, 2 minutes each.
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'''4.''' Serum Blocking: incubate sections with 10% normal serum blocking solution for 30 minutes to block non-specific binding of immunoglobulin.
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'''5.''' Primary Antibody: incubate sections with Primary antisera diluted 1:50 in 3% serum PBS, for 1 hour at room temperature to overnight 4C.
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'''6.''' Rinse in PBS washing buffer for 2 x 2 min.
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'''7.''' Secondary Antibody: incubate sections with conjugated secondary antibody 1:100-500  in 3% serum PBS, for 1 hour at room temperature.
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'''8.''' Rinse in PBS washing buffer for 3 x 2 min.
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'''9.''' Counter-stain in Gill´s formulation #2 hematoxylin for 5–10 seconds. Immediately wash with several changes of deionized H2O.
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'''10.''' Dehydrate: Soak in 95% ethanol 2x10 seconds, then 100% ethanol 2x10 seconds, then xylenes 3x10 seconds. Pipet 1–2 (5ul) drops of permanent mounting medium, cover with a glass coverslip and observe by light microscopy.
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==Controls==
==Controls==

Revision as of 15:25, 25 September 2008

Contents

Immunohistochemistry Protocol 1

John M. Sanders B.S. Cardiovascular Research Center, University of Virginia Charlottesville, VA.

The procedure below has been proven to be effective for labeling of PECAM-1, ICAM and VCAM using validated antibodies.

1. Deparaffinize and rehydrate 5 min tray

2 x xylene

2 x absolute ETOH

2 x 95 % ETOH

2 x 70 % ETOH

2 x milliQ H2O

1. Quench endogenous peroxidase activity

200 ml methanol + 3 ml (30% H2O2) in slide tub

  • make just before use, Incubate 30 minutes, RT

2a. wash H2O 5 min room temp.

1. Make up antigen unmasking solution (Vector Labs; 4oC) OR other antigen retrieval techniques

  • Shake well before measuring
  • 320 milliQ H2O + 3 ml unmasking solution
  • Mix by inversion

1. Rinse in milliQ H2O in tub

2. In slide tub with “fill” mark, fill all 24 slots in slide holder with “blank slides” if necessary, add unmasking solution to fill line, COVER and microwave for 20 minutes Replenish with dH20 at:

  • 15 minutes remaining
  • 11
  • 7
  • 3
  • 1

1. Cool slides in tub, covered, at room temp for 1 hour

2. During 1 hour, make up 0.5% FSGO (fish skin gelatin oil) in PBS (1 500 ml bottle PBS + 2.5 ml FSGO; allow 15 min for FSGO to come out of pipet)

3. Transfer to tub with plain room temperature PBS, 5 min

4. Make up avidin blocking solution:

For 1 ml:

  • 1 ml PBS/FSGO
  • 100 ul normal serum of same species as secondary antibody

4 drops avidin blocking solution (Vector Labs)

  • Invert tube to mix

5. Circle vessels with ‘pap pen’ ALWAYS KEEP SLIDES MOIST

6. Add blocking solution within circles; 1 hour in humidified chamber at room temperature

7. Aspirate off blocking solution

8. Add primary antibody to vessels on slides.

For 4 slides: antibody

  • PBS/FSGO 1 ml
  • normal serum 100 ul
  • biotin blocking solution (Vector Labs) 4 drops

9. Incubate 4 oC overnight in humidified chamber.

Day 2:

1. Aspirate primary antibody solution and wash in FSGO/PBS in tub for 5 min at room temperature; agitate 2. Make up secondary antibody:

per ml:

  • 5 ul secondary antibody
  • 100 ul normal serum
  • 1 ml FSGO/PBS

3. Blot slides with kimwipe and apply secondary antibody; incubate in humidified chamber 1 hour, room temperature

4. During incubation, make up ABC solution from kit: per ml:

  • 1 ml plain PBS
  • 20 ul A solution
  • 20 ul B solution

Allow to rock at room temperature for at least 30 min in order to form complex

5. Aspirate secondary antibody solution and wash in FSGO/PBS in tub for 5 min at room temperature; agitate

6. Blot slides and apply ABC; incubate 30 min at room temperature

7. Make up DAB solution: Approximately 30 min before using; add H2 O2 just before use

  • 10 ml plain PBS
  • 1 DAB tablet
  • 7.5 ul H2 O2 (30%)

Test DAB and ABC by adding small amount of DAB to a small amount of left over ABC, should turn dark brown immediately.

8. Wash with agitation in plain PBS, 5 min room temperature

9. Blot slides and apply DAB solution, incubate 5 min room temperature

10. Wash in dH20, 5 min room temperature

11. Counterstain in filtered (#1 Whatman) Hematoxylin I (not Mayer’s); 4-5 min

12. Rinse in running tap water until clear, 4-5 min. Return hematoxylin to bottle for reuse

13. Blueing if needed for 1 min; wash in tap water

14. Dehydrate, 5 minutes each:

  • 3 x absolute ETOH
  • 2 x xylene

15. Coverslip

Immunohistochemistry Protocol 2

1. Deparaffinize and rehydrate 5 min tray

2 x xylene

2 x absolute ETOH

2 x 95 % ETOH

2 x 70 % ETOH

2 x milliQ H2O

2. Antigen Retirieval

3. Rinse sections in 2 changes of PBS washing buffer in separate beakers, 2 minutes each.

4. Serum Blocking: incubate sections with 10% normal serum blocking solution for 30 minutes to block non-specific binding of immunoglobulin.

5. Primary Antibody: incubate sections with Primary antisera diluted 1:50 in 3% serum PBS, for 1 hour at room temperature to overnight 4C.

6. Rinse in PBS washing buffer for 2 x 2 min.

7. Secondary Antibody: incubate sections with conjugated secondary antibody 1:100-500 in 3% serum PBS, for 1 hour at room temperature.

8. Rinse in PBS washing buffer for 3 x 2 min.

9. Counter-stain in Gill´s formulation #2 hematoxylin for 5–10 seconds. Immediately wash with several changes of deionized H2O.

10. Dehydrate: Soak in 95% ethanol 2x10 seconds, then 100% ethanol 2x10 seconds, then xylenes 3x10 seconds. Pipet 1–2 (5ul) drops of permanent mounting medium, cover with a glass coverslip and observe by light microscopy.


Controls

  • chromogen only; no primary or secondary antibody
  • conjugate and chromogen control; no primary
  • biotinylated antibody, conjugate, chromogen control
  • Isotype control ( for monoclonal antibodies only)
  • Species control (ie. incubation with normal goat IgG)
  • Absorption control

References

  1. Barringhaus KG, Phillips JW, Thatte JS, Sanders JM, Czarnik AC, Bennett DK, Ley KF, and Sarembock IJ. . pmid:15153775. PubMed HubMed [Paper1]
  2. Manka D, Forlow SB, Sanders JM, Hurwitz D, Bennett DK, Green SA, Ley K, and Sarembock IJ. . pmid:15072990. PubMed HubMed [Paper2]
All Medline abstracts: PubMed HubMed
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