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What is immunohistochemistry?

Immunohistochemistry (IHC) combines anatomical, immunological and biochemical techniques for the identification of specific tissue components by means of a specific antigen/antibody reaction tagged with a visible label. IHC makes it possible to visualize the distribution and localization of specific cellular components within a cell or tissue.
The term immunohistochemistry is often used interchangeably with immunocytochemistry and immunostaining.

Coons and his colleagues (Coons et al 1941,1955; Coons and Kapland 1950) bound a fluorescent marker to an antibody and used the complex to identify antigens in tissue sections. Despite their relative age, the fluorescent probes are still widespread in use and with the advent of confocal microscopy, are experiencing a renaissance.
The basic immunocytochemical philosophy described by Coons and his colleagues of an antibody linked to a microscopically dense marker, has not altered, but the microscopically dense marking system has been developed for applications to a wide range of histological and electron microscope techniques, improvements have been made in protein conjugation, tissue fixation methods, detection labels and microscopes, making immunohistochemistry a routine and essential tool in many laboratories.

Nakane and Pierce, and Avrameas and Uriel, (Nakane and Pierce 1966; Avrameas and Uriel 1966) covalently linked the enzyme peroxidase, with the second antibody for use in histology. The peroxidase can be visualized by development with one of several different substrates to produce a brown, blue, or yellow reaction product. An increased sensitivity of the immunoperoxidase technique was achieved with the unlabelled antibody peroxidase anti-peroxidase (PAP) technique. The marker is a peroxidase complex of three proxidase molecules associated with two anti-peroxidase molecules. This technique gives a high signal, since three peroxidase molecules are associated with each antigen. Alkaline phosphatase can be used in a similar manner, alkaline phosphatase anti-alkaline phosphatase (APAAP) technique.

Most of the immunochemical staining methods in use today are based on the high affinity that (strept)avidin (Streptomyces avidinii) and avidin (chicken egg) have for biotin. Both possess four binding sites for biotin, but due to the molecular orientation of the binding sites, fewer than four molecules of biotin will actually bind. Because avidin is a glycoprotein and has an isoelectric point (pI) of 10, it has a propensity to non-specifically bind to lectin-like and negatively charged tissue components at physiological pH. It has been largely replaced today by streptavidin.

The inherent amplification of sensitivity made the avidin and streptavidin-biotin methods more desirable than the previously described PAP and APAAP methods.The basic sequence of reagent application consists of primary antibody, biotinylated secondary antibody, followed either by the preformed (strept)avidin-biotin-enzyme complex of the avidin-biotin complex (ABC) technique or by the enzyme-labelled streptavidin. Both conclude with the substrate solution. Horseradish peroxidase and alkaline phosphatase are the most commonly used enzyme labels. While the authors of the ABC method reported this procedure to have a greater sensitivity than the PAP method, Giorno subsequently found the sensitivity of a labelled avidin-biotin (LAB)method to be approximately four- to eight-fold greater than the ABC method. In both methods, the avidin has now been largely replaced by the use of streptavidin leading to the labelled streptavidin-biotin (LSAB) method and a modified ABC procedure, respectively.

One of the important goals in immunohistochemistry is to achieve greater sensitivity with detection systems using the shortest possible incubation time. However, multi-step detection systems have several drawbacks, such as complex time-consuming protocols, difficulties in standardization, suboptimal detection of hard to detect antigens, endogenous biotin activity, etc. Recently, new detection systems have been introduced using natural or synthetic polymer carriers that are coupled to linker antibodies. This approach increases the number of available enzymes or ligands binding at the antigenic site, thus increasing their reactivity with the chromogen. Because these systems avoid the use of (strept)avidin and biotin, nonspecific staining as a result of endogenous biotin is eliminated.

Immunohistochemistry, in situ hybridization, antigen retrieval, immunofluorescence, epitope retrieval.


HPV In Situ Hybridization, Cytokeratin Immunohistochemistry


Immunohistochemistry is a technique for identifying cellular or tissue constituents (antigens) by means of antigen-antibody interactions,
the site of antibody binding being identified either by direct labelling of the antibody, or by use of a secondary labelling method.

In Situ Hybridization techniques allow the demonstration of specific nucleic acid sequences (genes) in their cellular environment.

Above: Human Papillomavirus DNA demonstrated by In Situ Hybridization (pink)
in epithelial cells identified by indirect immunofluorescence using antibody against cytokeratin (green)



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  • CD56 ERIC NCAM on FFPWs

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  • Dewaxing slides for immunostaining

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  • Labeled Streptavidin Biotin (LSAB) General Method

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  • M. Tuberculosis on FFPET

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  • Microtubule-associated Protein, Neurone-specific in FFPWs

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  • Mowiol Mountant Firm set Immunofluorescence

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  • Neurofilament Protein Immunohistochemistry Staining Protocol ES/NexES

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  • Neurotactin in fly embryo FFPWs

  • Oct-2 Immunohistochemistry Staining Protocol ES/NexES

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  • Proteinase K Digestion

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  • Serotonin

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  • StABC (Streptavidin Biotin Complex Method)

  • streptABC Peroxidase Dako kit/DAB method for FFPWs for all species of primary Antibody

  • Streptavidin-Nanogold-Silver-Staining

  • SV40 T-Ag (Ab-1) Immunohistochemistry Staining Protocol ES/NexES

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  • Synaptophysin Immunohistochemistry Staining Protocol ES/NexES

  • Terminal Deoxynucleotidyl Transferase (TdT) Immunohistochemistry Staining Protocol ES/NexES

  • Toxoplasma Gondii Immunohistochemistry Staining Protocol ES/NexES

  • Trypsin Digestion

  • Trypsin Treatment

  • TTF-1 Immunohistochemistry Staining Protocol Autostainer (Cytospins)

  • Tyramide amplification ABC- DAB - Px method

  • Tyrosine hydroxylase in HIER FFPWs mouse

  • Vimentin Immunohistochemistry Staining Protocol Autostainer (Cytospins)

  • Vimentin Immunohistochemistry Staining Protocol ES/NexES

  • Von Willebrand Factor (Factor VIII) Immunohistochemistry Staining Protocol ES/NexES


  • Immunohistochemistry - In Situ Hybridization News:

  • A Simple, Reliable, and Sensitive Method for Multiple Immunoenzyme Staining

  • A Universal Antigen Retrieval Method

  • Abbott and BioGenex Enter Agreement for Automated Molecular Diagnostics System

  • ALCAM/CD166 in in breast cancer

  • Anaplastic Lymphoma Kinase (ALK)

  • Apoptosis, Cell Death and Cell Proliferation

  • Application of microarray technology in pulmonary diseases

  • Autofluorescence Eliminator Reagent

  • BCL-2

  • Biotinyl-tyramide-based In Situ Hybridization

  • Breast Carcinoma vs. Pulmonary Adenocarcinoma

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  • Collecting duct carcinoma of the kidney (CDC)

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  • Cyclin A and cyclin D1

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  • Cytopathology - from an Immunohistochemist’s Perspective

  • Dako goes Rabbit

  • DAX-1 expression in human breast cancer

  • Desmoplastic small round cell tumor

  • Differential Diagnosis of Cytokeratin “Dots”

  • Double-label Fluorescent Immunohistochemistry

  • Dual Fluorescent In Situ Hybridization and Immunohistochemical Detection

  • Endocervical vs. Endometrial Adenocarcinoma

  • Endogenous Biotin Artifact

  • Enhanced diagnostic immunofluorescence using biopsies transported in saline

  • Enrichment methods to detect bone marrow micrometastases

  • Epidermal Growth Factor Receptor and Erbitux

  • Evaluation of Follicular or Nodular Lymphoid Lesions

  • Evaluation of Hydropic Placentas (Hydropic Degeneration vs. Partial Mole vs. Com

  • Expression of pS2 in prostate cancer

  • FISH Solution for Lymphoma

  • HER-2/neu and c-Kit (CD117) in malignant melanoma

  • High Molecular Weight Cytokeratin (34βE12)

  • Histologic Spring 2004

  • hMLH1 and hMSH2

  • Human CD57+ germinal center-T cells

  • Human Herpesvirus Type 8 (HHV8)

  • ImmPRESS™ - New Staining System from Vector Laboratories

  • Immunohistochemistry

  • Immunohistochemistry in Amyloidosis

  • Immunohistochemistry in Clear Cell Carcinomas

  • Immunohistochemistry in DFSP vs. DF-FH

  • Immunohistochemistry in Lymph Node Histiocytosis

  • Immunohistochemistry in the Differential Diagnosis of Schwannoma and Neurofibrom

  • Immunohistochemistry in the Evaluation of Atypical Epithelial Cells in Effusions

  • Immunohistochemistry in thyroid carcinoma

  • Immunohistochemistry in Urothelial Dysplasia

  • Immunohistochemistry Staining Protocols

  • Immunostaining of imprint smears with the 'MCW melanoma cocktail'

  • Immunostains for b-catenin in Diagnostic Pathology

  • In Situ Hybridization

  • In Situ Hybridization with Nanogold-Streptavidin

  • Interleukin-2 and its receptor complex (a, ß and γ chains)

  • KATP channel subunits

  • Ki-67 clone K-2: A useful marker of fat cells and lipoblasts

  • MCM2

  • Metallothionein expression in renal cell carcinoma

  • Microarray analysis in clinical oncology

  • MMP-13 and TIMP-1 in head and neck squamous cell carcinomas

  • Multicolor-FICTION

  • New Instrument for Cancer Diagnostics

  • New Web site!

  • Oct3/4 A New Marker of Embryonal Carcinoma and Seminoma

  • ONE-STEP RNA probe synthesis templates

  • Optimal Titering of Primary Antibodies

  • p14ARF expression in invasive breast cancers and ductal carcinoma in

  • p16INK4a

  • p21WAF1/CIP1 and HER-2/ neu

  • p27Kip1

  • P504S (a-Methylacyl-CoA-Racemase)

  • p63

  • p63/P504S Antibody Cocktail in Prostate Biopsies

  • Perivascular Epithelioid Cell Tumores

  • Polysomy of chromosome 17 and overexpression of ERBB2

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  • Protein p16

  • Recognition of Early Myocardial Infarction

  • S100A7 (psoriasin) and Jab1 in ductal carcinoma in situ of the breast

  • Simultaneous Detection of EGFP and Cell Surface Markers by Fluorescence

  • TFE3 Immunostains in the Diagnosis of Alveolar Soft Part Sarcoma and Other Tumor

  • The Antigen–Antibody Reaction in Immunohistochemistry

  • The utility of cytokeratins 7 and 20 (CK7/20) immunohistochemistry

  • Tissue Protection Immunohistochemistry

  • Traps in Sentinel Lymph Node Biopsies

  • True Positive vs. False Positive Staining

  • Ubiquitin Immunohistochemistry in Alzheimer’s Disease

  • Ultrarapid Ki-67 immunostaining in frozen section interpretation of gliomas

  • UroVysion FISH

  • Utility of Ki-67 (MIB-1) Immunostaining in Cervical Biopsies

  • Utility of p16 (INK4a) Immunostaining in Cervical Biopsies

  • Vascular endothelial growth factor (VEGF)-C

  • Villin Immunohistochemistry

  • Wilms Tumor Gene Protein (WT1)

  • XHM

  • Xmatrx(TM)

  • ZAP-70 in Chronic Lymphocytic Leukemia


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  • Immunohistochemistry - In Situ Hybridization Topics / Posts:

  • About the TSA system (Perkin)

  • Abs towards human HLA class I antigens

  • Alu probe

  • anti-VP16 antibody

  • antibodies against C5b-9 Complement Terminal Complex

  • Antigen retreavel

  • Autofluorescence in rat brain tissue after lesions

  • Background problems

  • background problems with isotope probes

  • Background staining.

  • Base mismatch

  • Basic theory of ISH

  • bibliography about probe design

  • biotin blocking kits

  • bone problems

  • Bouin fixation with ISH

  • BrdU double labelling

  • Brdu in vivo @ in vitro

  • c-Kit antibody

  • CD3

  • CD38 Formalin Fixed Tissue

  • CD45 antigen not just in leukocytes??

  • Cells appear brown in BF microscopy in abscence of DAB

  • Citraconic Anhydride

  • Citraconic anhydride recipe

  • Colormetric detection and quantification

  • Combination ISH/Immunofluorescence

  • Compatibility of non-perfused tissue and Immuno...

  • Cross-Hybridization

  • Crystalline silica induced inflammation

  • Cyclin D2 detection

  • DAB Away Recipe

  • Debris after development

  • decalcification

  • Decalcification

  • decalcification

  • Disposal of used DAB solution

  • double immunofluorescence protocol about bone

  • Double Immunofluorescence with two mouse mAb

  • Draq5

  • Endogenous Alkaline Phosphatase

  • Factor XIIIa

  • Feulgen kit?

  • General in situ protocol

  • general info on ISH

  • Gold medal for Ole.........

  • Happy, belated, birthday Hogne!

  • help! anyone has experience of caveolin immunostaining

  • Hi Ventana users

  • how to design RNA probe

  • hyaluronic acid detection

  • hybridization buffer

  • Hybridization buffer recipes...

  • hydrolysis of probe

  • I just ordered some new Abs...need user comments, please

  • Immuno in frozen sections

  • immunofluorescence

  • Immunohistochem apoptotic markers

  • immunostaining H&E

  • In situ hybridization on culture cells

  • Interleukin 6

  • interleukins staining IHC

  • ISH for IFNgamma mRNA

  • ISH for new a gene

  • ISH in Bone

  • ISH on embryo cryosection

  • Ki-67 Quantitation in Mouse Bronchioles

  • Low signal with Isotopic In situ hybridization

  • MCM2

  • Melanin pigment removal

  • MLH-1

  • Most appropriate protein blocking solution ?

  • mouse probe

  • multi probes

  • Need some antibodies

  • new guy

  • New to IHC - startup equipment?

  • newbie Q: negative control is stained

  • Ole's New HRP kit

  • oligo dT hybridization to mRNA in stress granules

  • Organ Culture & BrdU

  • P53 immunistainning

  • per1 in hamster brains

  • perfusion of liver tissue

  • Phosphoantibodies

  • pink background with DIG staining

  • Poly d(T) probe

  • Positive sense probe

  • Problem with erys

  • problem:precipitate/debris with any chromogen

  • Problems with Staining

  • Problems with the background...IHC in chick embryos

  • protocol ER beta

  • protocols

  • radioactive in-situ

  • radioactive in-situ hybridization

  • Resources to locate those proficient in immunohistochemistry

  • Sensitive TSA ISH combined with IHC

  • Signal amplification

  • slide-coating protocol

  • Some problem in signal....

  • storage

  • Storing fixed cells

  • TMA artifact

  • transcription factor in mouse lymphoid tissue sections

  • Trilogy Ag retrieval soln

  • trouble with ISH

  • Urovysion-SpectrumGold Problems

  • Very Basic Question

  • what label?

  • Which is more specific?

  • Whole mout in situ hybridization using 60mer oligos

  • WT1 and PTEN


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  • EBER In Situ Hybridization and CD20 Immunohistochemistry - PowerPoint presentation of Epstein Barr Virus (EBER) In Situ Hybridization combined with CD20 Immunohistochemistry

  • EBER In Situ Hybridization and CK Immunohistochemistry - PowerPoint presentation of Epstein Barr Virus (EBER) In Situ Hybridization in combination with Cytokeratin Immunohistochemistry.

  • EBER In Situ Hybridization and Kappa/Lambda Double Immunofluorescence - PowrPoint presentation of Epstein Barr Virus (EBER) In Situ Hybridization combined with Kappa and Lambda Light Chain Double Immunofluorescence

  • HPV In Situ Hybridization and CK Immunohistochemistry - PowerPoint presentation of Human Papilloma Virus (HPV) In Situ Hybridization combined with Cytokeratin Immunofluorescence

  • Immuno Gold Silver Technique - PowerPoint presentation of Immuno Gold Silver (IGS) Technique.

  • Immunohistochemistry vade mecum - An excellent piece of work by Dr. Paul W. Bishop You can search for tumours to find out their pattern of immunoreactivity or look for individual antibodies to check their specification. There are links to all the references through PubMed. This amazing programme is small, easy to install and runs on any PC.
    To download the latest version, go to author's Home Page

  • LSAB Technique - PowerPoint presentation of Labelled Streptavidin Biotin (LSAB) Technique.

  • Non Biotin Amplification - PowerPoint presentation of Non Biotin Amplification using Fluorecein-labelled antibody.

  • PAP Technique - PowerPoint presentation of Peroxidase Anti-Peroxidase (PAP) Technique

  • Polymer Detection - PowerPoint presentation of Polymer Detection.

  • Technical Immunohistochemistry - TECHNICAL IMMUNOHISTOCHEMISTRY: Achieving Reliability and Reproducibility of Immunostains.
    By Rodney T. Miller, M.D. Director of Immunohistochemistry ProPath Laboratory, Inc.


  • Immunohistochemistry - In Situ Hybridization Web Links:

  • 2J2 Mouse/Human Paraffin - Detection of2J2 in formalin-fixed, paraffin-embedded mous and human tissues

  • 2J5 in Formalin-Fixed, Paraffin-Embedded, Mouse Tissue - Detection of 2J5 in Formalin-Fixed, Paraffin-Embedded, Mouse Tissue

  • 35S-labeled probe - In Situ Hybridization using 35S-labeled probe, Detection by emulsion or film autoradiography. Frozen Sections.

  • A New Blocking Method for Application of Murine Monoclonal Antibody to Mouse Tissue Sections - A New Blocking Method for Application of Murine Monoclonal Antibody to Mouse Tissue Sections

  • A New Rapid Immunohistochemical Staining Technique Using the EnVision Antibody Complex - A New Rapid Immunohistochemical Staining Technique Using the EnVision Antibody Complex

  • A Novel Quality Control Slide for Quantitative Immunohistochemistry Testing - We introduce a novel quality control technology that may improve intra- and interlaboratory immunohistochemistry (IHC) standardization. The technology involves the creation of standardized antibody targets that are attached to the same slides as the patient sample. After IHC staining, the targets turn the same color as the stained cells or tissue elements. Unlike current clinical practice, our proposed targets are neither cells nor tissue sections.

  • Abcam - Mission:"...to build the largest catalog of the best antibodies in the world"

  • Abgent - Abgent develops innovative reagents and technologies to profile post-translational modifications of the proteome.

  • Accurate Chemical & Scientific - Accurate has specialized in products for basic and R&D research as well as routine laboratory work. Polyclonal and monoclonal antibodies

  • Acris - Where ever your research interests may be and what ever animal model you work with you will have a good chance to find what you need.

  • Advanced ImmunoChemical Inc. - Immunological Reagents worldwide for diagnostics sector & research needs.

  • Advances in Cytochemical Methods for Detection of Apoptosis - Key Words: apoptosis, cytochemistry, TUNEL, ISNT, annexin V, caspases, ricin

  • Affinity BioReagents - ABR—Affinity BioReagents, a privately held corporation, offers over 1,800 industry leading research reagents and custom antibody production services to the worldwide research community. The ABR product portfolio includes primary and secondary antibodies, proteins, peptides and viral expression kits supporting 30 distinct research areas. Cutting-edge antibody production services allow researchers the flexibility to create a custom antibody to meet their specific research needs.

  • Alexa Dyes, a Series of New Fluorescent Dyes that Yield Exceptionally Bright, Photostable Conjugates - We report here the superior, largely unparalleled fluorescence emission and photostability of conjugates of a new series of sulfonated compounds named Alexa 350, Alexa 430, Alexa 488, Alexa 532, Alexa 546, Alexa 568, and Alexa 594 dyes. The number in each of their names refers to the approximate excitation maxima of the dyes, which nearly match the principal wavelength of several commonly used excitation sources. All of the Alexa dyes exhibit pH-insensitivity over a very broad range, and those that absorb at wavelengths greater than 480 nm have the high molar extinction coefficient typical of fluoresceins or rhodamines.

  • Alexis - Apoptosis, Cell Cycle & DNA Transactions, Combinatorial Chemistry Reagents, Cytoskeletal Research, Growth Factors, Cytokines & Chemokines, Immunology & Cancer Research, Neurochemicals, Nitric Oxide & Oxidative Stress, Signal Transduction.

  • Alpha Diagnostic International - Alpha Diagnostic Intl., Inc., (ADI) located in San Antonio, Texas, USA, is one of the major providers of custom services such as peptides synthesis, and polyclonal antibodies. ADI maintains an USDA inspected and approved, animal facility. We have NIH/OPRR Assurance on file. Other antibody related services (affinity purification, conjugation to enzymes, dyes, fluorochromes, etc, ELISA, Western blots) are also provided.

  • Amplification Methods to Increase the Sensitivity of In Situ Hybridization - Here we outline the principles of tyramide signal amplification using the catalyzed reporter deposition (CARD) technique, present practical suggestions to efficiently enhance the sensitivity of ISH with CARD, and discuss some applications and possible future directions of in situ nucleic acid detection using such an amplification strategy.

  • An Optimized Method for ISH with Signal Amplification That Allows the Detection of Rare mRNAs - Using biotinyl–tyramide and streptavidin conjugated to alkaline phosphatase (AP) to introduce an additional round of amplification, we have now achieved a considerable enhancement of signal intensity relative to standard chromogenic ISH detection systems. We term this protocol TSA-AP (tyramide signal amplification using AP). In addition, we have optimized critical parameters to improve hybridization with digoxigenin (DIG)-labeled probes and to reduce nonspecific binding of probes, both strategies being essential for successful detection of rare mRNAs.

  • Anderson Lab In Situ Hybridization Protocols - In Situ Hybridization of Frozen Sections, Whole Mount In Situ Hybridization, In Situ Hybridization on Cultured Cells and Additional Techniques

  • Anti-Human CD Antibodies - Anti-Human CD Clustered Antibodies

  • Anti-Mouse CD Antibodies - Anti-Mouse CD Clustered and other Antibodies

  • Anti-Rat CD Antibodies - Anti-Rat CD Clustered and other antibodies

  • Antibodies - Structure and Sequence - This page attempts to summarise useful information on antibody structure and sequence. It provides a query interface to the Kabat antibody sequence data, general information on antibodies and crystal structures and links to other antibody-related information.

  • Antibody Directory - We are striving to include as many companies or products as possible, but we do not make a claim to being comprehensive.

  • Antibody Purification Handbook - The purpose of this handbook is to present the most effective and most frequently used strategies for sample preparation and purification of the many different forms of antibodies and antibody fragments used in the laboratory.

  • Antibody Staining of Drosophila Adult Retina - The following protocol has been adapted from Larry Zipursky's lab. It detects antigen in retinas that have been sectioned in plastic.

  • Antibody Structure - Antibody Structure - nicely illustrated

  • Antigen Retrieval by Heating En Bloc for Pre-fixed Frozen Material - This article describes a simple alternative method for AR that can be used for aldehyde-fixed frozen sections.

  • Antigen Retrieval Immunohistochemistry - Antigen Retrieval Immunohistochemistry: Past, Present, and Future

  • Antigen Retrieval in Prion Protein Immunohistochemistry - Many different protocols for the detection of prions in brain tissue have been used. Thus far, picric and/or formic acid, steam autoclaving at 121C of sections, microwave treatment, and 4 M guanidine thiocyanate treatment have been suggested. The objective of our experiment was to obtain the standard pretreatment(s) resulting in optimal immunostaining. In the experiment, successive tissue slides of brain specimens of several Creutzfeldt–Jakob disease and control patients were stained using different combinations of pretreatments.

  • Antigen Retrieval of Basement Membrane Proteins from Archival Eye Tissues - Antigen retrieval (AR) methods can unmask tissue antigens that have been altered by fixation, processing, storage, or resin interactions. This is particularly important in the study of archival tissues, because primary fixatives and storage times may vary among specimens.

  • Antigen Retrieval Techniques - Antigen Retrieval Techniques: Current Perspectives

  • Antigen Retrieval Trial for Post-embedding Immunoelectron Microscopy by Heating - Antigen Retrieval Trial for Post-embedding Immunoelectron Microscopy by Heating with Several Unmasking Solutions

  • APC Formalin-Fixed Paraffin-Embedded MouseTissue - Identification of Adenomatous Polyposis Coli in Formalin-Fixed Paraffin-Embedded MouseTissue

  • Application of Microwave Technology - Application of Microwave Technology to the Processing and Immunolabeling of Plastic-embedded and Cryosections

  • Applied Immunohistochemistry & Molecular Morphology - Applied Immunohistochemistry & Molecular Morphology provides complete coverage of the diagnostic and prognostic applications of immunohistochemistry (IHC), its contributions to the understanding of the biology of tumors and other lesions, and the technical aspects of setting up a laboratory and interpreting results.

  • ASMA(1A4) - ASMA (1A4) Optimax Immunostainer

  • ASMA(1A4) - ASMA (1A4) Immunohistochemistry Staining Protocol Techmate. NordiQC

  • ASMA(1A4) - ASMA(1A4) Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • Assay Designs - Antibodies for research and diagnostic purposes (Immunoassays and Kits)

  • Assessment of Methods for Tissue-Based Detection of the HER-2/neu Alteration in Human Breast Cancer - Assessment of Methods for Tissue-Based Detection of the HER-2/neu Alteration in Human Breast Cancer: A Direct Comparison of Fluorescence In Situ Hybridization and Immunohistochemistry

  • Aurion - AURION is a research oriented company dedicated to and specializing in the development and production of Ultra Small ImmunoGold Reagents, Silver Enhancement Reagents, Blocking Reagents, Incubation Solutions and Conventional ImmunoGold Reagents

  • Autoradiography for mRNA detection in mouse embryo tissue sections - Protocols from Oxford Practical Approach Series

  • B-Catenin - Identification of B-Catenin in Formalin-Fixed, Paraffin Embedded Rodent Tissue

  • Bcl-2 - Bcl-2 clone 124 staining Immunohistochemistry Staining Protocol Ventana Nexes. NordiQC

  • Bcl-2 - Bcl-2 clone bcl-2/100/D5 Staining Immunohistochemistry Staining Protocol Autostainer, DakoCytomation. NordiQC

  • Bcl-2 - Bcl-2 clone 100 Staining Immunohistochemistry Staining Protocol I6000, BioGenex. NordiQC

  • Bcl-2 - Bcl-2 clone 8C8 Staining Immunohistochemistry Staining Protocol LabVision Immunostainer. NordiQC

  • BCL2 - BCL2 Immunohistochemistry Staining Protocol Autostainer

  • BCL2 - BCL2 Immunohistochemistry Staining Protocol Techmate. NordiQC

  • BCL6 - BCL6 Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • Beecher Instruments - Beecher develops microarray technologies that facilitate high-throughput genomic and proteomic research. Offers automated and manual tissue microarray instruments and accessory tissue arrayer products.

  • Beta Polymerase - Identification of Beta Polymerase by an 8K Domain Antibody in Paraffin Embedded Rodent Tissue

  • Biocare Medical - BIOCARE is a unique manufacturer and supplier of immunostaining systems, histopathology products, monoclonal and polyclonal antibodies and automated staining equipment.

  • Biogenesis - Operating from the South Coast of England and New Hampshire in the US we are able to offer a wide range of Custom Services, in addition to our comprehensive catalogue of over 6,000 products.

  • BioGenex - BioGenex offers a broad range of reagents, detection kits, antibodies, probes, special stains, tissue microarrays, automated staining and imaging systems to streamline and standardize cellular and molecular analysis.

  • Biognostik - Supplier of custom-designed, high-quality ANTISENSE sequences and HybriProbes™ for in situ hybridization.

  • BioLegend - We offer products covering the areas of cell immunophenotyping, cytokines and chemokines, adhesion, phosphorylation, cancer research, cell-cycle analysis, and apoptosis. Our aggressive product development program, through technology licensing, collaborations, and internal hybridoma development, produces strategic reagents for use in a variety of applications including flow cytometry, ELISA, immunoprecipitation, Western blotting, immunofluorescence microscopy, immunohistochemistry, and in vitro / in vivo functional assays.

  • BioMed Central - BioMed Central. Over 100 Open Access journals covering all areas of Biology and Medicine

  • Biomeda - Full range of detection kits, a diversified line of monoclonal and polyclonal antibodies,

  • BIOMOL International - BIOMOL offers a range of biochemicals with applications in signal transduction, immunohistochemistry, gene regulation, apoptosis, neuroscience and drug discovery. In addition to purified enzymes, antibodies, and assay kits, BIOMOL’s innovative products include Nupherin-neuron transfection reagent, Fluor de Lys HDAC assay kit, and Screen-Well compound libraries. www.biomol.com 800-942-0430

  • Biosource - Biosource International, Inc. is a broad based life sciences company focused on providing solutions in the areas of functional proteomics and advanced drug discovery through the development, manufacturing, marketing, and distribution of unique biologically active reagent systems which facilitate, enable, and accelerate pharmaceutical development as well as biomedical research.

  • Biotin and Digoxigenin as Labels for Light and Electron Microscopy in Situ Hybridization Probes - Biotin and Digoxigenin as Labels for Light and Electron Microscopy in Situ Hybridization Probes: Where Do We Stand?

  • Biotinylation of Antibodies - Biotin is used in two-step detection systems in concert with conjugated avidin. Biotin is typically conjugated to proteins via primary amines (i.e., lysines). Usually, between 3 and 6 biotin molecules are conjugated to each antibody.

  • Biotrend - BIOTREND is specialised in Immunology, Neuroscience, Pharmacology and Radiochemistry, supplying biomedical and pharmaceutical research with a large range of antibodies, radiolabelled products, custom synthesis and antibody production services.

  • BRDU Mouse - Detection of BRDU in formalin-fixed, paraffin-embedded mouse tissue

  • BRDU Rat - Detection of BRDU in formalin-fixed, paraffin-embedded rat tissue

  • Calbindin-D-28K in Formalin-Fixed Paraffin-embedded Mouse Tissue - Detection of Calbindin-D-28K in Formalin-Fixed Paraffin-embedded Mouse Tissue

  • Calcium-induced Modification of Protein Conformation Demonstrated by Immunohistochemistry - Calcium-induced Modification of Protein Conformation Demonstrated by Immunohistochemistry: What Is the Signal?

  • Calgranulin in Formalin-Fixed, Paraffin Embedded Rat Tissue - Identification of Calgranulin in Formalin-Fixed, Paraffin Embedded Rat Tissue

  • Calretinin - Calretinin Immunohistochemistry Staining Protocol DakoCytomation Horizon. NordiQC

  • Calretinin clone 5A5 - Calretinin clone 5A5 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • Calretinin in Formalin-Fixed, Paraffin Embedded Rodent Tissue - Identification of Calretinin in Formalin-Fixed, Paraffin Embedded Rodent Tissue

  • Cambio - STAR*FISH Chromosome Painting

  • Capralogics - Capralogics produces high quality polyclonal antibodies. Chemokine Receptors, Interleukins, Nuclear Components, Apoptosis, Cell Membrane, Protein Kinases, Signaling Intermediates, Lymphocyte Signaling

  • Carcinoembryonic antigen (CEA) - Carcinoembryonic antigen (CEA) Immunohistochemistry Staining Protocol DakoCytomation Autostainer

  • Catalase in Formalin-Fixed, Paraffin Embedded Rat Tissue - Detection of Catalase in Formalin-Fixed, Paraffin Embedded Rat Tissue

  • Cayman Chemical - Cayman Chemical Company is helping make research possible by supplying scientists worldwide with biochemical tools in research disciplines such as cancer, nitric oxide, neuroscience, apoptosis, oxidative injury, endocrinology, and much more. We specialize in assay kits for the measurement of eicosanoids, free radical biomarkers, cyclic nucleotides, cytokines, hormones and nitric oxide. In addition, Cayman offers a broad range of quality biochemicals including eicosanoids, nitric oxide reagents, and a variety of related lipids, fatty acids, enzymes, and antibodies.

  • CC10 using LSAB Kit in Formalin-Fixed, Paraffin Embedded Rodent Tissue - Identification of CC10 using LSAB Kit in Formalin-Fixed, Paraffin Embedded Rodent Tissue

  • CD10 - CD10 clone 56C6 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD10 - CD10 clone 56C6 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD10 is expressed in a subset of chromophobe renal cell carcinomas - CD10 has been considered a useful marker in the diagnosis of renal carcinomas, because of its expression in clear cell and papillary renal cell carcinomas and its absence in chromophobe renal cell carcinomas.

  • CD117 (c-kit) - CD117 (c-kit) Polyclonal, Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD117 (c-kit) - CD117 (c-kit) Polyclonal, Immunohistochemistry Staining Protocol DakoCytomation TechMate

  • CD117 (c-kit) - CD117 (c-kit) Polyclonal, Immunohistochemistry Staining Protocol Ventana BenchMark. NordiQC

  • CD117 (c-kit) - CD117 (c-kit) Polyclonal, Immunohistochemistry Staining Protocol DakoCytomation TechMate. NordiQC

  • CD14 - CD14 clone 7 Protocol

  • CD14 - CD14 clone 7 Immunohistochemistry Staining Protocol TechMate

  • CD15 - CD15 clone MMA Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD15 - CD15 clone Tu9 Immunohistochemistry Staining Protocol GenoMx i6000, BioGenex. NordiQC

  • CD15(C3D-1) - CD15(C3D-1) Immunohistochemistry Staining Protocol Autostainer LabVision

  • CD20 - CD20 clone L26 Immunohistochemistry Staining Protocol DakoCytomation Horizon. NordiQC

  • CD20 Expression in Hodgkin and Reed-Sternberg Cells of Classical Hodgkin’s Disease - CD20 can be expressed in Hodgkin and Reed-Sternberg (HRS) cells of classical Hodgkin’s disease (HD), but its clinical significance remains controversial. Therefore, we correlated CD20 expression with presenting features and clinical outcome of untreated patients with classical HD.

  • CD23 - CD23 clone 1B12 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD23 - CD23 clone 1B12 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD23 - CD23 clone 1B12 Immunohistochemistry Staining Protocol Ventana NexES. NordiQC

  • CD23 - CD23 clone MHM6 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD3 - CD3 clone PS1 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD3 Polyclonal - CD3 Polyclonal Immunohistochemistry Staining Protocol Dako TechMate

  • CD30 - CD30 clone Ber-H2 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD30 - CD30 clone Ber-H2 Immunohistochemistry Staining Protocol DakoCytomation TechMate. NordiQC

  • CD30 - CD30 clone Ber-H2 Immunohistochemistry Staining Protocol Ventana NexES. NordiQC

  • CD30 - CD30 clone Ber-H2 Immunohistochemistry Staining Protocol DakoCytomation TechMate

  • CD30 - CD30 clone Ber-H2 Immunohistochemistry Staining Protocol Ventana BenchMark. NordiQC

  • CD31 - CD31 clone JC/70A Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD31 - CD31 clone JC/70A Immunohistochemistry Staining Protocol DakoCytomation TechMate. NordiQC

  • CD31 - CD31 clone JC/70A for Autostainer. NordiQC

  • CD31 - CD31 clone JC/70A Immunohistochemistry Staining Protocol Ventana BenchMark. NordiQC

  • CD34 - CD34 clone QBEnd 10 Immunohistochemistry Staining Protocol Labvision Autostainer. NordiQC

  • CD34 - CD34 clone My10 Immunohistochemistry Staining Protocol DakoCytomation TechMate

  • CD34 - CD34 clone QBEnd 10 manual protocol. NordiQC

  • CD34 - CD34 clone QBEnd 10 for DakoCytomation Autostainer. NordiQC

  • CD40 in Formalin Fixed Paraffin Embedded Mouse Tissue - Detection of CD-40 in Formalin Fixed Paraffin Embedded Mouse Tissue

  • CD40 in Frozen Mouse Tissue - Detection of CD-40 in Frozen Mouse Tissue

  • CD5 (4C7) - CD5 (4C7) Immunohistochemistry Staining Protocol Autostainer Lab Vision. NordiQC

  • CD5 (4C7) - CD5 (4C7) Immunohistochemistry Staining Protocol Ventana NexES. NordiQC

  • CD5 (CD5/54/F6) - CD5 (CD5/54/F6) Immunohistochemistry Staining Protocol DakoCytomation Autostainer

  • CD68 - CD68 clone KP1 for DakoCytomation Autostainer. NordiQC

  • CD68 - CD68 clone KP1 Immunohistochemistry Staining Protocol Ventana NexES. NordiQC

  • CD68 - CD68 clone PG-M1 for Ventana NexES. NordiQC

  • CD68 - CD68 clone PG-M1 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • CD79a - CD79a clone JCB117 Immunohistochemistry Staining Protocol LabVision Autostainer. NordiQC

  • CD79a - CD79a clone JCB117 for Ventana NexES. NordiQC

  • CD99 - CD99 (12E7) NordiQC

  • CD99 (12E7) - CD99 (12E7) Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • CEA - CEA (ll-7) Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • CEA - CEA (ll-7) Immunohistochemistry Staining Protocol Ventana Benchmark. NordiQC

  • CEA - CEA (Col-1) Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • Cedarlane Laboratories - Complement, Lympholyte cell separation media, cell purification Immunocolumns and a wide range of Antibodies. Custom Antibody Services.

  • Cell Marque - Antibodies, Bio Reagents, Detection Systems and Declere/Trilogy

  • Cell Pellet Protocol - Special Techniques Cell Pellet Protocol

  • Cell Signaling Technologies - Signal Transduction Research

  • Cemines - Antibodies to different transcription factors

  • Chemicon - Broad range of antibodies.

  • Chick, mouse, and Xenopus two colour whole mount ISH - Protocols from Oxford Practical Approach Series. Chick, mouse, and Xenopus two colour whole mount in situ hybridization staining with Fast Red and TrueBlue

  • Chromogranin A - Chromogranin polyclonal, Immunohistochemistry Staining Protocol DakoCytomation Autostainer

  • Chromogranin A - Chromogranin clone LK2H10 Immunohistochemistry Staining Protocol DakoCytomation Autostainer. NordiQC

  • Chromogranin A - Chromogranin Polyclonal. Immunohistochemistry Staining Protocol LabVision Autostainer. NordiQC

  • Chromogranin A - Chromogranin clone LK2H10+PHE5 Immunohistochemistry Staining Protocol LabVision Immunostainer. NordiQC

  • Chromogranin A - Chromogranin clone LK2H10 + PHE5 Staining Immunohistochemistry Staining Protocol LabVision Immunostainer. NordiQC

  • Chromogranin A - Chromogranin A clone LK2H10 Staining Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • Chromogranin A - Chromogranin A (polyclonal) Staining Immunohistochemistry Staining Protocol Autostainer. NordiQC

  • Chromogranin A in Formalin-Fixed, Paraffin-Embedded Mouse Tissue - Identification of Chromogranin A in Formalin-Fixed, Paraffin-Embedded Mouse Tissue

  • Chromosome In Situ Hybridization using biotin labeled probes - Chromosome In Situ Hybridization using biotin labeled probes. Preparation of Chromosome Squashes

  • Chromosome preparation for ISH - Chromosome preparation for in situ hybridization (ISH)

  • Co-labeling Using In Situ PCR - Co-labeling Using In Situ PCR: A Review

  • Co-Localization of Multiple Antigens and Specific DNA - Co-localization of proteins and nucleic acid sequences by in situ hybridization and immunohistochemistry is frequently difficult as the process necessary to detect the target structure of one technique may negatively affect the target of the other. Morphological impairment may also limit the application of the two techniques on sensitive tissue. To overcome these problems we developed a method to perform in situ hybridization and immunohistochemistry on semithin sections of methyl methacrylate-embedded tissue.

  • Complete Chromogen Separation and Analysis in Double Immunohistochemical Stains Using Photoshop - Complete Chromogen Separation and Analysis in Double Immunohistochemical Stains Using Photoshop-based Image Analysis

  • Conjugation of monoclonal antibodies - In this series of web pages, protocols, notes, and various illustrations are given to aid in the conjugation of proteins--principally monoclonal antibodies--to fluorescent dyes. These conjugation procedures are commonly performed in our laboratory--we have conjugated several hundred different monoclonals using almost all of the various dyes listed. The procedures are relatively straightforward and require only minimal familiarity with standard laboratory techniques (gel filtration and spectrophotometry are the most difficult!).

  • Control of Autofluorescence of Archival Formaldehyde-fixed, Paraffin-embedded Tissue - Confocal laser scanning microscopy (CLSM) offers the advantage of quasi-theoretical resolution due to absence of interference with out-of-focus light. Prerequisites include minimal tissue autofluorescence, either intrinsic or induced by fixation and tissue processing, and minimal background fluorescence due to nonspecific binding of the fluorescent label. To eliminate or reduce autofluorescence, three different reagents, ammonia–ethanol, sodium borohydride, and Sudan Black B were tested on para