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AB103742

AEC Single/Plus (30ml)

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(1 Publication)

AEC Single/Plus (ab103742) is a single, highly stable AEC chromogen/substrate working solution used in peroxidase-based detection systems in IHC.

- Ready-to-use solution.
- Less toxic nature as compared to DAB.
- Reduces waste: Unused solution does not need to be immediately discarded.
2 Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - AEC Single/Plus (30ml) (AB103742)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - AEC Single/Plus (30ml) (AB103742)

AEC Single/Plus staining Cytokeratin 5 & 14 in tonsil tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - AEC Single/Plus (30ml) (AB103742)
  • IHC-P

Unknown

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - AEC Single/Plus (30ml) (AB103742)

Formalin fixed paraffin embedded Human tonsil stained with HMW Cytokeratin antibody (ab850) labeled with AEC Single/Plus (30ml) (ab103742) produces a robust red color.

Key facts

Product details

Mono AEC/Plus is a single, highly stable AEC chromogen/substrate working solution. When used in conjugation with immunoperoxidase detection systems, AEC produces a red colored and product at positive sites, yeilding strong contrast when combined with a blue hematoxylin counterstain. Specimens stained using Mono AEC/Plus cannot be dehydrated in ethanol and musy be mounted in an aqueous-based mounting medium.

ab103742 is a single, stable ready for use solution. The solution is light sensitive and must be protected from exposure to light and stored in an opaque bottle or dark environment.

Protocol

  1. Once section have been incubated with peroxidase, wash with wash buffer.

  2. Wipe slides removing excess buffer. Add enough drops of Mono AEC/Plus to cover tissue sections.

  3. Incubate for 5-15 minutes at room temperature. For optimal results, observe reaction under the microscope for signal developmant. Once the desired signal to noise ratio is acheived, stop the reaction by washing the slides in DI H2O.

AEC Single/Plus is a single, highly stable AEC chromogen/substrate working solution. When used in conjugation with immunoperoxidase detection systems, AEC produces a red colored and product at positive sites, yeilding strong contrast when combined with a blue hematoxylin counterstain. Specimens stained using AEC Single/Plus cannot be dehydrated in ethanol and must be mounted in an aqueous-based mounting medium.

AEC Single/Plus (ab103742) is a single, stable ready for use solution. The solution is light sensitive and must be protected from exposure to light and stored in an opaque bottle or dark environment.

Protocol

  • Once section have been incubated with peroxidase, wash with wash buffer.
  • Wipe slides removing excess buffer. Add enough drops of AEC Single/Plus to cover tissue sections.
  • Incubate for 5-15 minutes at room temperature. For optimal results, observe reaction under the microscope for signal developmant. Once the desired signal to noise ratio is acheived, stop the reaction by washing the slides in DI H2O.

Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
Please refer to protocols

Product protocols

Target data

Publications (1)

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European journal of nuclear medicine and molecular 46:2178-2189 PubMed31264169

2019

Discovery and preclinical characterization of [F]PI-2620, a next-generation tau PET tracer for the assessment of tau pathology in Alzheimer's disease and other tauopathies.

Applications

Unspecified application

Species

Unspecified reactive species

Heiko Kroth,Felix Oden,Jerome Molette,Hanno Schieferstein,Francesca Capotosti,Andre Mueller,Mathias Berndt,Heribert Schmitt-Willich,Vincent Darmency,Emanuele Gabellieri,Cédric Boudou,Tanja Juergens,Yvan Varisco,Efthymia Vokali,David T Hickman,Gilles Tamagnan,Andrea Pfeifer,Ludger Dinkelborg,Andreas Muhs,Andrew Stephens
View all publications

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