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Merck
CN

21627-M

IHC Select Proteinase K

别名:

Antigen/ Epitope Retrieval Reagent

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关于此项目

eCl@ss:
42029053
UNSPSC Code:
41116010
NACRES:
NA.51
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packaging

pkg of 15 mL

manufacturer/tradename

Chemicon®, IHC Select

technique(s)

immunohistochemistry: suitable (paraffin)

Quality Level

Application

For use as a Pretreatment Reagent in Immunohistochemical staining procedures. Use Proteinase K to retrieve Epitopes in formalin-fixed, paraffin-embedded tissue sections mounted on glass microscope slides. This procedure is performed after deparaffinization and prior to IHC.



Warm to room temperature before use. Digestion time and dilution should be determined by user as concentration is dependent on the type of antibody, antigen, and fixation method used. Recommended starting dilution range: Neat to 1:30.



For best results use this reagent in conjunction with other IHC Select detection reagents. A complete list of reagents is available at www.chemicon.com.

Physical form

Liquid Proteinase K containing 15mM sodium azide as a preservative. Discard if it becomes cloudy or contaminated.

Preparation Note

When stored at 2-8°C, the Proteinase K is stable up to the expiration date printed on the label. Do not freeze or expose to elevated temperatures.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

存储类别

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Aisan Farhadi et al.
The European journal of neuroscience, 56(1), 3755-3778 (2022-05-06)
Diabetes mellitus may cause tau protein hyperphosphorylation and neurodegeneration, but the exact mechanism by which diabetic conditions induce tau pathology remains unclear. Tau protein hyperphosphorylation is considered a major pathological hallmark of neurodegeneration and can be triggered by diabetes. Various

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