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Home > Services > TMA-IHC(researchers supply TMA slides and primary antibody)

TMA-IHC(researchers supply TMA slides and primary antibody)

Cat No.GDP1002

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  • slide
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Introduction 

Tissue microarrays (TMA) is to make different individual tissues arrange regularly on a slide. The customer provides us single tissue or paraffin blocks and we provide the production service of TMA according to the requirement of different diameters of blots, different numbers and different arrangement. IHC is a research based on the principle of antigen and antibody specific binding,making the chromogenic reagent (enzyme) color of the labeled antibody by chemical reaction,in order to determine the intracellular antigen (polypeptide and protein),and make the positioning, qualitative and quantitative analysis.


TMA-IHC combines two technologies, gathered the advantages of both.

 

Protocol

1.1 TMA deparaffinize and rehydrate: incubate sections in 3 cylinders of xylene, 15 min each. Dehydrate in 2 cylinders of pure ethanol for 5 min, followed by dehydration in gradient ethanol of 85% and 75% ethanol, respectively 5 min each. Wash in distilled water.

 

1.2 Antigen retrieval: immerse the slides in Sodium citrate antigen retrieval solution (pH 6.0) and maintain at a sub-boiling temperature for 8 min, standing for 8 min and then followed by another sub-boiling temperature for 7 min. Be sure to prevent buffer solution evaporate. Let air cooling. Washing three times with PBS (pH 7.4) in a Rocker device, 5 min each.

 

1.3 Block endogenous peroxidase: Washing three times with PBS (pH 7.4) in a Rocker device, 5 min each. Immerse in 3% H2O2 and incubate at room temperature for 15 min, keeping in dark place. Then washing again three times with PBS (pH 7.4) in a Rocker device, 5 min each.

 

1.4 Block with serum: Eliminating obvious liquid, marking the objective tissue with liquid blocker pen. Cover objective tissues with 10% normal rabbit serum (for the case of primary antibody originated from goat) or 3% BSA (for the case of primary antibody originated from others) at room temperature for 30 min.

 

1.5 Primary antibody: Throwing away the blocking solution slightly. Incubating slides with primary antibody (diluted with PBS appropriately) overnight at 4 ℃, placing in a wet box containing a little water.

 

1.6 Secondary antibody: Washing slides three times with PBS (pH 7.4) in a Rocker device, 5 min each. Then throwing away liquid slightly. Cover objective tissue with secondary antibody (appropriately respond to primary antibody in species) labelled with HRP, incubating at room temperature for 50 min.

 

1.7 DAB developing: dry sections slightly, add fresh prepared DAB chromogenic reagent to marked tissue. Manage reaction time by observing in microscopy until nucleus shows brown-yellow. Then stop developing reaction by washing in running tap water.


1.8 Counterstain in nucleus with Hematoxylin staining solution for 3 min and wash in tap water. Treat with the differentiate solution for a few seconds, wash in running tap water. Back to blue by bluing solution, wash in running tap water.

 

1.9 Dehydrate successively in gradient ethanol of 75%, 85%, and 2 cylinders of pure ethanol, respectively 6 min each. Clearing in xylene for 5 min and mount with resin mounting medium.

 

Results  

Nucleus stained with hematoxylin are blue. The positive cells developed by DAB reagent have brown-yellow nucleus.


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