| Background |
The polyhistidine (His) tag is an amino acid motif that consist of six histidine residues which are added at the C-terminus or N-terminus of recombinant protein for affinity purification.
High-quality monoclonal anti-His antibodies are offered by Miltenyi Biotec either coupled to µMACS™ MicroBeads for specific isolation of His-tagged proteins on an analytical scale or conjugated to biotin, FITC, or horseradish peroxidase (HRP) for analysis of recombinant His-tagged protein. |
| Isolation and detection of His-tagged proteins |
Isolation of His-tagged proteins
The µMACS™ Anti-His Isolation Kit takes advantage of the well-established MACS® Technology; thus, allows fast and specific isolation of pure His-tagged proteins. The advantages of MACS Technology for protein isolation are:
Specificity – high-quality monoclonal antibodies coupled to MACS MicroBeads assure specific isolation of His-tagged proteins with low background.
Sensitivity – fast reaction kinetics of tiny (50 nm), non-sedimenting MACS MicroBeads allow sensitive isolation even when working with rare proteins.
Speed – less than 2 hours to high-purity His-tagged proteins!
For medium- to large-scale purification of His-tagged proteins the ProCatch His Resin is recommended (fig. 1).
Detection of His-tagged proteins
The monoclonal Anti-His antibody is available with various conjugates. The fluorochrome-conjugated (FITC or PE) Anti-His antibodies enable an immunofluorescence analysis e.g. by fluorescence microscopy or FACS (fig. 2). Various detection methods are applicable using the biotinylated Anti-His antibody in combination with appropriate streptavidin conjugates.
For specific and sensitive detection of His-tagged proteins by Western blot or ELISA analysis the Anti-His-HRP and the Anti-His-HRP (C-term.) are available. Directly coupled to horseradish peroxidase (HRP), both antibodies simplifiy these immunological assays as incubation with secondary antibodies is not necessary. The Anti-His-HRP (C-term.) shows even higher sensitivity and specificity for C-terminal His-tagged proteins than the Anti-His-HRP. The latter detects both N- and C-terminal His-tagged proteins.
Antibody specificatins
Target: His epitope (HHHHHH)
Isotype Anti-His antibody: mouse IgG2b
Isotype Anti-His antibody (C-terminal): mouse IgG1 |
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| Figure 1 |
| Purification of a 30 kDa histidine-tagged protein from prokaryotic cell lysate with ProCatch His Resin. Marker (lane 1), lysate from bacterial extract (2), the flow-through (3), and the eluate (4) were separated by SDS-PAGE and Coomassie stained. |
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| Figure 2 |
| Intracellular labeling and FACS analysis of mPD1-His expressing CHO cells. CHO cells were transiently transfected with a mPD1-His encoding vector and analysed by flow cytometry. CHO cells were fixed, permeabilized and labeled with Anti-His-FITC (B) or Mouse IgG1-FITC isotype control (A), respectively. |
| A |
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| B |
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