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Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

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Department of Physiology and Biophysics, University of California, Irvine (UCI)

 

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Cite this Article: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

Chi, V., Chandy, K. G. Immunohistochemistry: Paraffin Sections Using the Vectastain ABC Kit from Vector Labs. J. Vis. Exp. (8), e308, doi:10.3791/308 (2007).

Abstract: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

Immunohistochemistry (IHC)는 집중 / 특정 항체를 사용하여 마운트된 조직 섹션에서 단백질 표현을 시각화하기 위해 활용 가치 기법입니다. 직접 및 간접 방법 : 두 가지 방법이 있습니다. 본 실험에서는, 우리는 간접 IHC의 얼룩의 사용을 설명합니다. 간접 IHC의 얼룩은 매우 구체적인 기본 및 비오틴 - 복합 이차 항체를 활용합니다. 차 항체는 이차 항체가 아닌 구체적인 배경에 대한 얼룩 빼기 및 기본 항체에 단지를 형성하여 신호를 증폭하는 동안 몰래, 특정 에피토프에 바인딩하여 관심 단백질을 식별하는 이용하고 있습니다. 슬라이드는 어느 냉동 섹션에서 생성된, 또는 파라핀 임베디드 섹션은 유리 슬라이드에 장착할 수 있습니다. 이 프로토콜에서는, 우리는 내생 퍼옥시데이즈 활동이 아닌 특정 바인딩 사이트 알코올 기울기를 사용하여 dewaxing, 수화, 열 유도 항원 검색 및 차단하여 파라핀 - 임베디드 섹션의 준비에 대해 설명합니다. 일부 섹션은 다음 T 세포 마커 CD8 특정 항체 물들일하고 다른 사람은 티로신 hydroxylase에 대한 스테인드하는 동안. 슬라이드는 이후 비오틴에 복합 적절한 보조 항체로 처리되며, 다음과 같은 기판 Diaminiobenzidine (DAB)로 아비딘 - 복합 양고추냉이 퍼옥시데이즈 (HRP)를 활용하여 개발하였습니다. 개발 다음, 슬라이드가 대비를위한 counterstained 있으며, permount와 coverslips 이하 탑재. 충분한 건조 후 다음 슬라이드 다음 이미지에 대한 준비가되어 있습니다.

Protocol: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

파라핀 섹션의 염색법

  1. Dewax 각 5 분 배 크실렌 (피셔 X3 S -4)로 슬라이드 (사용에 따라 매월 변경 크실렌, 크실렌은 독성입니다.) 피셔 심판 08-812 - 1A 및 랙에서 20 슬라이드에 요리와 커버를 사용하여 이러한 요리를 맞게했다. 접시 당 200 ML 액체.
  2. (모든 이주 경사도를 변경) 다음과 같이 알코올 기울기를 통해 하이드 레이트 :
    • 2 분 각각에 대해 100 %의 에탄올 (피셔 # A406 - 20)의 2 배
    • 2 분 각 95 % 에탄올에 2 배
    • 2 분 70 %의 에탄올에 1X
    • 1X 2 분 50 % 에탄올에
    • 1X 2 분 30 %의 에탄올에
    • 2 분 1X ddH 2 O
  3. 5 분 DPBS의 소크 (DPBS = Dulbecco의 수정 인산이 칼슘 2 살린 버퍼 +와 MG 2 +).

항원 복구 :

  1. 전자렌지에 미리 열을 나 - 구연 산염 완충액 (10 MM, 산도 6.5).
  2. 전자 레인지에서 15 분 슬라이드를 요리. 슬라이드 이렇게 모든 분을 확인하고 필요한 경우 나이 - 구연 산염 추가 건조하지 않습니다.
  3. 실온에서 냉각하자.
  4. 1% 20 분 대한 DPBS에서 H 2 O 2 (30 % 주식의 1.5 ML 시그마 50 ML의 DPBS에서 H - 1009).과 내생 퍼옥시데이즈 활동 블럭
  5. DPBS 3 X 5 분에서 만끽해보세요.
  6. 4 ° DPBS에서 C + 5% 소 혈청 알부민 (BSA) + 0.1 % 나 Azide + 5% 혈청에서 하룻밤 잠복기가 아닌 특정 사이트를 차단합니다.

    참고 : 혈청 중 선택이 얼룩에 사용되는 항체가 만들어진하는 종류에 따라 달라집니다. 보조 AB가 (비오틴에 복합)되었다있는 수종의 혈청과 차단합니다. 이 사용할 수없는 경우, 기본 AB가되었다하는 것과 다른 종 혈청 사용합니다.

  7. 아비딘 / 비오틴 차단 키트 (벡터 실험실 카탈로그 # SP - 2001)와 비오틴 사이트를 차단 :
    • 15 분 아비딘 D와 부화. DPBS로 간단히 씻어.
    • 15 분 대한 비오틴 솔루션과 부화.
  8. DPBS에 상온에서 2 시간, + 2% BSA + 0.1 % NaAzide + 혈청 2% (단계를 차단과 같은)에 대한 기본 AB에 품어.
  9. PBS 3 X 5 분에서 만끽해보세요.
  10. DPBS에서 실온 + 2% BSA + 0.1 % 나 Azide + 혈청 2퍼센트 (차단 단계에 사용되는 동일). 1 시간 동안 비오틴과 복합 보조 AB와 부화
  11. 이것을 사용하기 전에 최소한 30 분 개발할 수 있기 때문에 동시에 ABC 시약을 준비! (자료 참조)
  12. 50 ML 원뿔 관에 준비합니다. 15 ML의 DPBS에서 (없음 묘약, 아니 azide) 시약 3 방울을 추가, 믹스 및 시약의 B와 믹스 3 방울을 추가합니다. 병 쥐어 않도록, 오히려 자신의 양식에 방울 기다립니다. 벡터 실험실에서 ABC 키트 Vectastain PK - 6100.
  13. DPBS 3 X 5 분에서 만끽해보세요.
  14. 실온에서 30-45 분 ABC 시약과 부화.
  15. DPBS 3 X 5 분에서 만끽해보세요.
  16. (자료 참조) 사용하기 전에 즉시 유리관 5 ML ddH 2 O에서 (벡터 실험실 #은 SK - 4100) DAB 퍼옥시데이즈 기판 준비
    • 버퍼 주식 솔루션 2 방울, 혼합
    • DAB 4 방울, 혼합 (약간 갈색이 될해야합니다)
    • 2 방울 H 2 O 2, 믹스
  17. 슬라이드 위에 DAB 기판을 드롭과 갈색 얼룩 살펴보십시오.
  18. 얼음 파고 슬라이드 + 반응을 중지 수돗물.
  19. 5 분 차가운 수돗물에 따라 헹굼.
  20. Hematoxylin (20 초, 피셔 CS401 - D)와 Counterstain과 물이 빠져나가 올때까지 수돗물에 씻어.
  21. 알코올 기울기는 100 % 에탄올 (2 분 각)으로 30 % 에탄올로 최대 시작을 통해 탈수.
  22. 크실렌 3 X 5 분에서 만끽해보세요.
  23. Permount와 마운트 (피셔 # SP15 - 100) : 슬라이드에있는 섹션 위의 일부를 넣고 기포없이 coverslip으로 섹션에 천천히 누르십시오. ~ 24 시간이 소요되는, 완전히 건조까지 coverslip를 이동하지 마십시오.

Disclosures: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

Materials: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

Name Company Catalog Number Comments
Xylene Fisher Scientific X3S-4 Change xylene every month depending on use. Xylene is TOXIC.
100% ethanol Fisher Scientific A406-20 Use to make EtOH gradient.
DPBS Dulbecco’s modified Phosphate Buffered Saline WITH Ca2+ and Mg2+
Na-Citrate buffer 10 mM, pH 6.5
H2O2 Sigma-Aldrich H-1009 30% stock => Dilute to 1% in DPBS
Blocking solution DPBS + 5% bovine serum albumin (BSA) + 0.1% Na Azide + 5% serum.
BSA
Sodium Azide NaAzide
avidin/biotin blocking kit Vector Laboratories SP-2001
Ab buffer DPBS + 2% BSA + 0.1% Na Azide + 2% serum (same as used for the blocking step)
ABC kit Vectastain PK-6100 Vector Laboratories
DAB peroxidase substrate Vector Laboratories SK-4100
ddH2O
Hematoxylin Fisher Scientific CS401-D counterstain
Permount Fisher Scientific SP15-100
Slides and cover-slips glass

Ask the Author: Immunohistochemistry : 벡터 연구소에서 Vectastain ABC 키트를 사용하여 파라핀 섹션

15 Comments

What is the purpose of dehydrating in ethanol and soaking in xylene before mounting the coverslips?

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Posted by: AnonymousOctober 1, 2008, 4:06 PM

By dehydrating and soaking in xylene, the tissue is properly dehydrated prior to application of permamount. Without this step, the permamount would take longer to dry, and the coverslip would most likely slide during visualization. I've also noticed that visualization of the slides prior to curing of the permamount increases the amount of air bubbles formed when the slide is over the lamp.

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Posted by: AnonymousOctober 20, 2008, 5:29 PM

purpose of citrate wash

 

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Posted by: arun r gMarch 18, 2009, 4:53 AM

Boiling the sample in the sodium citrate solution allows for heat induced antigen retrival. However, this step is not always necessary, and is highly dependent upon the antigen or epitope you are attempting to stain for.

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Posted by: AnonymousMay 19, 2009, 6:01 PM

I have a problem with ABC kit, because it is expired, how many time can i use the kit after it expired.

If i put the unmasking in hot bath and it is in boiling point, the results change? what is the chemistry principle of unmasking use.

And i habe trouble with GFAP because it has nonespecific marking with neurons and don´t mark astrocites i think that is the time of incubation of primary antibody. but what can I do?

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Posted by: Karolina OchoaMay 19, 2009, 3:29 PM

Hi Karolina,

I am from Vector Labs, manufacturer of the ABC kit described in the video. My name is Craig Pow and I head the technical service department. We were invited to respond to your inquiries by the management at JoVE to perhaps offer you some insightful information as we are very familiar with the product of course.

You have written essentially three inquiries. From our perspective, none of them are particularly in reference to the video and two of them do not pertain to the Vectastain ABC detection reagents. Regardless, we hope the following information is helpful.

The Vectastain ABC kits are given a guaranteed workable shelf-life of 12 months from the time of receipt. We know the kits will work well without any loss of sensitivity or performance during this time period when stored appropriately at 4 degrees Celcius. It has been our experience, and that of many investigators, that this one year timeframe is by no means a "drop dead" date. In other words, the ABC kits can be used well beyond this one year date, in some cases two to three years, again without any loss of performance. The reagents in the kits are very stable under the refrigerated conditions and this is true for the numerous Vectastain ABC kits we offer that consist of concentrated and Ready-To-Use formats with different enzyme systems. You do not state which Vectastain ABC kit you have or how long the product has been expired, so I do not think we can provide you with further specifics.

The following recently published references should provide you with details and current opinions regarding antigen unmasking in immunohistochemistry:

1) Shi, S.R. et al (2007) J. Histochem. Cytochem. 55(2):105-109

2) Leong, T. Y-M. and Leong, A. S-Y. (2007) Adv. Anat. Pathol. 14(2):129-131

3) D'Amico, F. et al (2009) J. Immunol. Methods 341(1-2):1-18

Your third inquiry appears to be more of a question concerning specificity of the primary antibody rather than a background staining issue. Indeed primary antibodies directed against GFAP (glial fibrillary acidic protein) should bind to astrocytes. From your stated observations the primary antibody is not recognizing the correct cell type in your tissue. I am unclear if you are applying antigen unmasking techniques in this application. Certainly inappropriate antigen unmasking parameters (such as the salt used, pH, temperature, time) may alter tissue properties to generate inaccurate staining. This is where positive and negative controls would be vitally important to validate the staining results on the test sections. Primary antibody incubation times for standard sections cut at < 10 micrometers usually run around 30 to 60 min at room temperature. In some cases overnight incubation at 4 degrees Celcius is required where poor affinity or avidity for the target antigen occurs. We do offer a Troubleshooting Guide in pdf format on our website that describes controls to use in the absence of staining or if background staining is a problem. We hope you find this Guide and the information presented here helpful.

Regards,

Craig Pow

 

 

 

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Posted by: Craig PowMay 21, 2009, 4:20 PM

I wish to know what is the concentration of haematoylin you prepared? Is it Myer's or Gill's?

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Posted by: AnonymousMay 21, 2010, 12:04 PM

The hematoxylin solution is Gill's #2, diluted 1:1 with dd water. The catalog number from Fisher is: CS401-1D

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Posted by: AnonymousAugust 4, 2010, 1:42 PM

I also wish to know what is the most proper antibody dilution to use initially to try

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Posted by: AnonymousMay 21, 2010, 12:08 PM

The concentration depends on the antibody you are using. Check the packing information. Appropriate concentrations can range from 1:100 to 1:100,000. I would initially try 1:100, then work with more dilute solutions.

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Posted by: AnonymousAugust 4, 2010, 1:30 PM

Tissue in parrafin block has been kept in fridge for 8 months. Can I still use for immunohistochemistry staining of p53?

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Posted by: Arifah A.May 27, 2010, 4:36 AM

Was the sample formalin treated prior to paraffin embedding? If so, the sample should be fairly stable, but the only way to confirm would be to use controls while staining your experimental sections.

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Posted by: AnonymousAugust 4, 2010, 1:35 PM

My Vectastain elite ABC kit and DAB substrate had expired in August 2009. Can I still use them as I only need small quantity for my samples?
Regards
Yassir

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Posted by: yassirAugust 4, 2010, 12:06 AM

I would contact Vector labs regarding the stability of their product post their printed expiration date.

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Posted by: AnonymousAugust 4, 2010, 1:37 PM

The timing shown here in this video differs from the timing of protocols given in Vector Lab protocols.
Please advise

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Posted by: MilanOctober 7, 2010, 9:31 PM

I would follow the Vector labs timing, then adjust as needed if the results are not clear.

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Posted by: VictorApril 24, 2011, 12:54 PM

queria v~e em português não entendo inglês

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Posted by: cely granja de oliveira April 11, 2011, 11:49 AM

Olá Cely Granja de Oliveira,

No momento nós não temos traduções disponíveis em Português. Sinto muito. Você pode utilizar os serviços de Tradução de Google para traduzir o texto.

Obrigado,
-Chris

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Posted by: Chris Macdonald J.April 11, 2011, 12:30 PM

give me information about acute lymphoblastic leukemia(ALL)?by RT(Reverse transcriptase PCR) or role of RT PCR in acute lymphoblastic leukemia(ALL)?

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Posted by: Dr.Sadia NeelamApril 24, 2011, 9:54 AM

Can any one send me the drawing of the taste sensors in tong with, example: salt, sweet, sour, bitter & umami?

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Posted by: Jayatissa LiyanageApril 30, 2011, 10:35 PM

How much secondary biotynilated antibody should I use if I use 1:100 dilution of the primary? I cannot figure it out with the drops...

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Posted by: JelenaJuly 26, 2011, 12:40 PM

Many commercially available secondary antibodies have information indicating the effective concentration for different applications. For example, Western Blotting may require a 1:10,000 dilution, while an ELISA may require a 1:1000 dilution. You can test different concentrations on your samples to assure that you're not at the plateau for signal response. Use enough volume to cover the sample. Use of more volume will not change the secondary antibody concentration.

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Posted by: AnonymousJuly 26, 2011, 1:26 PM

Although I have done IHC in a variety of forms in the past, this excellent video was ideal as a refresher. Victor--thank you so much for your clear, patient and very thorough description of the technique. I will be using a PAP pen for the first time soon and it was extremely helpful to watch you demonstrate how to use it.

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Posted by: helenAugust 16, 2011, 11:52 AM

Hi,
I have questions: first is the antigen retrival, I'm using proteinase K from DAKO icubation time (3 min) instaed of heating process, however, it seems that the tissue morphology somehow changed my question is is that because the incubation time? or because of the concentration?

my second question: In the dehydration step before mounting the coverslips, if the tissue happened to dry-out completely before mounting the coverslips would that affect the tissue or not?

Thank you

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Posted by: Redha October 4, 2011, 5:00 PM

Proteinase K usage for antigen retrieval is sensitive to time and concentration due to over digestion. Changes is tissue morphology could be attributed to either.
Allowing the tissue to dry out completely prior to mounting may affect the morphology of the tissues dependent on the tissue being analyzed.

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Posted by: AnonymousNovember 7, 2012, 8:11 PM

Is the coplin jar polypropylene or can glass??

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Posted by: Marcia L.July 18, 2012, 2:26 PM

Not sure if our jars were polypropylene or polyethylene, but we have used them and glass coplin jars without any significant difference.

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Posted by: AnonymousNovember 7, 2012, 8:00 PM

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