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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).
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.
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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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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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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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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.
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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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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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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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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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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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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?
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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.
What is the purpose of dehydrating in ethanol and soaking in xylene before mounting the coverslips?
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ReplyPosted by: AnonymousOctober 1, 2008, 4:06 PM