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Two different detection systems are provided:

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1. detection via Strep-Tactin^® conjugates (for Strep-/Twin-Strep-tag^® proteins)
2. detection via monoclonal antibodies against Strep-/Twin-Strep-tag^®

Read which detection system is suitable for your applications:

For direct detection of Strep-tag^® fusion proteins in Western blots use:

• via chromogenic and/or chemiluminescence reaction (no secondary antibody needed!) use
  - Strep-Tactin^® HRP conjugate (HRP, horseradish peroxidase)
  - StrepMAB-Classic HRP conjugate

• via chromogenic reaction
  - Strep-Tactin^® AP conjugate (AP, alkaline phosphatase)

For protein detection in ELISA use:

For nearly irreversible binding of StrepMAB-Immo, the Strep-tag® must be N-terminally extended by a SerAla linker (recombinant protein - SA-WSHPQFEK or SA-WSHPQFEK - recombinant protein).

Monopoly live casino. Visualize your Strep-tag^® protein Strep-Tactin^®XT, StrepMAB-Classic, or StrepMAB-Immo fluorescent conjugates. They are available with:

For nearly irreversible binding of StrepMAB-Immo, the Strep-tag® must be N-terminally extended by a SerAla linker (recombinant protein - SA-WSHPQFEK or SA-WSHPQFEK - recombinant protein).

For staining (Twin-) Strep-tagged proteins in FACS we recommend to use:

Oregon lottery results. For nearly irreversible binding of StrepMAB-Immo, the Strep-tag® must be N-terminally extended by a SerAla linker (recombinant protein - SA-WSHPQFEK or SA-WSHPQFEK - recombinant protein).

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