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Other Reagents
tcnt3138
tcnt3138
Hematoxylin Stain, Mayer Modified
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AVAILABLE SIZES
500ml
$
0.00
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ORDERING INFORMATION
International
TAICLONE BIOTECH CORP.
order@taiclone.com
+886-2-2735-9682
+886-2-2735-9807
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Western blot (WB)
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Product Description
Hematoxylin Stain, Mayer Modified is a ready to use
progressive hematoxylin that does not require filtering and does not
contain chloral hydrate or alcohol. Due to the progressive staining nature
of Mayer hematoxylin, over-staining is less likely and an acid alcohol
differentiation step is not required in the staining process. Mayer
hematoxylin is an excellent choice as a counterstain in
immunohistochemistry (IHC), amyloid and copper staining procedures.
The routine hematoxylin and eosin (H&E) stain is used for screening
specimens in anatomic pathology, as well as for research, smears, touch
preps and other applications. Its two primary coloring agents stain all
cellular material including nuclei (blue), and cytoplasmic elements (pinkred). Popularity of this stain is due, in large measure, to its simplicity,
ability to clearly demonstrate a wide variety of different tissue
components, dependability, repeatability, and speed of use.
Information
Application
IHC, Blood Cells stain
Specifications
No Data Available
Misc Information
Notes
PROTOCOL: H&E STAINING PROCEDURE WITH MAYER MODIFIED:
1. Deparaffinize sections thoroughly in three changes of xylene, 3 minutes each. Hydrate through two changes each of 100% and 95% ethyl alcohols, 10 dips each. Wash well with distilled water.
2. Stain with Hematoxylin Stain, Mayer Modified, 10 to 20 minutes, depending on preference of nuclear stain intensity.
3. Wash well in tap water for 3 minutes.
4. Blue slides in Lithium Carbonate, Saturated Aqueous or Scott Tap Water Substitute for 10 dips.
5. Wash in three changes of tap water; rinse in distilled water.
6. Drain excess water from rack/slides; proceed to 70% alcohol for 10 dips.
7. Counterstain in Eosin Y Working Solution or prepared Eosin-Phloxine Working Solution for 30 seconds to 3 minutes, depending on preference of intensity.
8. Dehydrate in two changes of 95% ethyl alcohol for 1 minute each and two changes of 100% ethyl alcohol, 10 dips each. Clear in three changes of xylene, 10 dips each; coverslip with compatible mounting medium.
RESULTS:
Nuclei : Blue
Erythrocytes and eosinophilic granules : Bright pink to red
Cytoplasm and other tissue elements : Various shades of pink
Protocol
Fixation: Formalin 10%, Phosphate Buffered
Technique: Paraffin sections cut at 5 microns
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