Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic...

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Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides http://bioquant-com.bioquantusers.org/ products.php? page=ls&content=gallery&sub=feulgen

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Page 1: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.

Staining Techniques

Histochemical Stains: involve chemical reactions

Feulgen reaction -DNA

Periodic Acid Shiff (PAS)

-neutral and acidic

polysaccharides

- glycogen, mucous, basal

laminae

http://bioquant-com.bioquantusers.org/products.php?page=ls&content=gallery&sub=feulgen

Page 2: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.

Goblet cells PAS stainIntestinal Villus

Page 3: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.

Carbohydrate-rich Basal Laminae stain with PAS stain

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Staining Techniques

Localization (staining) of an enzyme

AB + T AT + BENZYME

generate visible product

provide substrate

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Staining Techniques

AB + T AT + B

Acetylcholinesterase- neuromuscular junction

ACETYLCHOLINESTERASE

Other stains for ATPases, alkaline phosphatases, and others

Page 6: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.

A technique to localize specific molecules in an organ, tissue or cell.

IMMUNOCYTOCHEMISTRY

Page 7: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.

An organism creates antibodies to foreign molecules, ANTIGENS.

An antigen may have different regions, EPITOPES, that are recognized as foreign

by an organism.

First, a bit of immunology……….

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Page 9: Staining Techniques Histochemical Stains: involve chemical reactions Feulgen reaction -DNA Periodic Acid Shiff (PAS) -neutral and acidic polysaccharides.
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Polyclonal antibodies

-A collection of distinct types of antibody molecules that recognize the same antigen (antibodies A + B + C)

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Monoclonal antibodies-A single type of antibody molecule that recognizes only

one epitope on an antigen (antibody A OR B OR C)

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• Polyclonal antibodies•ADVANTAGES: recognize more epitopes in

tissue•DISADVANTAGES: less specificity

• Monoclonal antibodies•ADVANTAGES: more specific•DISADVANTAGES: reduced signal possible

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EXPERIMENT:

- Homogenize a sample of human muscle containing a variety of cells (muscle cells, neurons, capillaries, connective tissue cells).

- Inject homogenate into a mouse.

WHAT HAPPENS IN THE MOUSE?

-Take of sample of mouse blood, extract the serum, stain a section of human muscle.

WHAT WILL BE STAINED IN THE HUMAN MUSCLE?

HOW DO WE GET STAINING OF ONLY MUSCLE MYOSIN?

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Representative myosin heavy chain (MHC) immunocytochemistry images of an emphysematous diaphragm after co-incubation with anti-laminin antibody and an antibody against one of the adult MHC isoforms.

Antibody against lamininAntibodies against different epitopes of myosin heavy chain

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IMMUNOCYTOCHEMISTRY Use of antibodies to detect specific

molecules (antigens) in a tissue

Antibody binds to an antigen in the tissue.

ANTIGEN

ANTIBODY

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IMMUNOCYTOCHEMISTRYDirect Immunocytochemistry: a visible marker is

directly attached to antibody binding the antigen

The antibody is conjugated to visible marker.

•Fluorochrome

•Enzyme (HRP)•Electron dense molecule (ferritin, gold)

Procedure: Fix the tissueRinse with saline solutionIncubate with conjugated antibodyRinseMount on slide, view with microscope

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DIRECT IMMUNOCYTOCHEMISTRY

ADVANTAGESSpecificityLess background staining

DISADVANTAGESLow sensitivity if the antigen is present in the

tissue in low concentrations.

Need to directly conjugate marker to antibody.

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INDIRECT IMMUNOCYTOCHEMISTRY– Primary antibody binds to the antigen.

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INDIRECT IMMUNOCYTOCHEMISTRY– Primary antibody binds to the antigen.– Secondary antibody binds to the primary antibody.– Secondary antibody is conjugated to a visible

marker.

Procedure: Fix the tissueRinseIncubate unlabeled primary antibodyRinseIncubate labeled secondary antibodyRinseMount on slide, view with microscope

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INDIRECT IMMUNOCYTOCHEMISTRY

ADVANTAGESAmplification of the signalCan use labeled secondary with different

primary antibodies

DISADVANTAGESThe nonspecific background may increaseTakes longer to doNeeds more reagents

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LIMITATIONS OF IMMUNOCYTOCHEMISTRY

Cross-reactivitySensitivityAntigenicity

-Frozen sections

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Antibodies (immunoglobulins) of specific species are used as antigens to generate secondary antibodies.

ANTIGEN--> mouse antibody

Rabbit anti-mouse IgG

Goat anti-mouse IgG

Donkey anti-rabbit IgM

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QUESTION: Dr. Reist is studying the distribution of two proteins, FasII and spectrin in neurons. She would like to label both molecules in the same sample using double-labeling immunocytochemistry. She has these antibodies:

Primary antibodies: Secondary antibodies:

rabbit anti-FasII mouse anti-rabbit-FITC(fluorescein)

mouse anti-FasII donkey anti-rabbit-FITC

goat anti-FasII rat anti-mouse-Rh (rhodamine)

rat anti-spectrin goat anti-mouse-Rh

rabbit anti-spectrin rabbit anti-Goat-Rh

donkey anti-spectrin

What primary and secondary antibodies will successfully distinguish the distribution of FasII and spectrin in the same preparation?

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AUTORADIOGRAPHY

• Tissue with radiolabeled

molecule

• Cover with photo emulsion

• Radiation activates silver ->

silver grains

• Develop and view

http://course1.winona.edu

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In situ hybridization

Labeled DNA or RNA probe

Why?

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In situ hybridization

Labeled DNA or RNA probeRadioactive tag

Digoxigenin

Incubation with tissueAutoradiography or Immunocytochemistry

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www-bioc.rice.edu/bios576/immuno/immuno.html

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Whole mount in situ hybridization views on E10.5 mouse embryos with Phox2a (A), En1 (B), Uncx4.1 (C) and Lmx1b (D) RNA-probes.Juha PartanenInstitute of Biotechnology, P.O.Box 56, FI-00014 Univ. of Helsinki

Fluorescence in situ hybridization of the all-human telomere probe, (T2AG3)n, to chromosome ends of the Pacific oyster (Crassostrea gigas).www.hsrl.rutgers.edu/mapping.html