Hematoxylin and Eosin (H&E) Staining Kit,Aqueous

Hematoxylin and Eosin (H&E) Staining Kit,Aqueous

Cat: RA20141

Size1:2x100mL     Price1:$50
Size2:2x500mL     Price2:$150

Category: Pathology Staining Kits Tags: ,

Product Introduction

Hematoxylin and eosin (H&E) staining is the most fundamental staining method in routine histopathology, widely used in pathology, teaching, and scientific research. Hematoxylin is a natural alkaline dye extracted from logwood (Haematoxylon campechianum), appearing as light yellow-brown crystals. After oxidation, it forms hematein, which, together with a mordant (commonly trivalent aluminum or iron salts), stains cell nuclei. H&E staining is used to observe the morphological structure of normal and pathological tissues, and to identify abnormal substances or specific components in cells and tissues. Special staining, enzyme histochemistry, and immunohistochemistry are all performed based on the observation of H&E-stained sections. In H&E-stained sections, nuclei appear blue and cytoplasm appears red, providing a clear contrast for easy observation and analysis.

EnkiLife Hematoxylin and Eosin Staining Solution uses high-purity imported hematoxylin and oxidizing agents, free of harmful substances such as mercuric oxide and methanol. It provides excellent nuclear staining with minimal precipitation and metal film formation. It is widely applicable to human, animal, veterinary, and aquatic samples, and can be used for paraffin-embedded sections, frozen sections, and cytological smears. Both hematoxylin and eosin solutions can be reused. 


Basic Information

Product   name

Hematoxylin and Eosin (H&E) Staining Kit, Aqueous

Sizes

2x 100 mL, 2x 500 mL

Storage

RT

Shipping

RT

Validity

12 months


Product Components

Components

2x 100mL

2x 500mL

Reagent (A): Hematoxylin Staining   Solution

100 mL

500 mL

Reagent (B): Eosin   Staining Solution (Aqueous)

100 mL

500 mL


Notes

1. Dewax sections thoroughly; if temperature is low, incubate at 60–70 °C in an oven.

2. Replace graded ethanol solutions regularly.

3. Differentiation time with hydrochloric acid ethanol should be adjusted according to section thickness, tissue type and age; ensure adequate washing with tap water after differentiation to remove all acid.

4. Ether-ethanol mixed fixative is prepared by mixing equal volumes of ether and 95% ethanol, adding a small amount of acetic acid, and storing in a sealed container.

5. Keep staining times as short as possible for frozen sections.

6. Common bluing solutions include 0.2–1% ammonia water, Scott’s tap water substitute, or 0.1–1% lithium carbonate solution.

7. For your safety and health, wear a lab coat and disposable gloves during operation.


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