Product Description
Size: 30mL
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.
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
Once section have been incubated with peroxidase, wash with wash buffer.
Wipe slides removing excess buffer. Add enough drops of Mono AEC/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 H
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 H
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
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Collaboration
Tony Tang
Email: Tony.Tang@iright.com
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