CoA 488

 

  • This product was discontinued on 09/14/2017

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S9348
  • Discontinued
    Discontinued
  • Product Information
    CoA 488 is a photostable fluorescent substrate used to label ACP-tag and MCP-tag fusion proteins exposed on the surface of living cells. This cell-impermeable CoA substrate is based on the ATTO-TEC dye ATTO 488, and is suitable for standard fluorescein filter sets. It has an excitation maximum at 506 nm and an emission maximum at 526 nm. This package contains 50 nmol of CoA 488 substrate, sufficient to make 10 ml of a 5 μM ACP-tag or MCP-tag fusion protein labeling solution.

    The ACP-tag and MCP-tag are small protein tags (8 kDa) based on the acyl carrier protein. MCP-tag contains two mutations (D36T and D39G). Both allow the specific, covalent attachment of virtually any molecule to a protein of interest. Substrates are derivatives of coenzyme A (CoA). In the labeling reaction, the substituted phosphopantetheine group of CoA is covalently attached to a conserved serine residue of the ACP-tag or the MCP-tag by a phosphopantetheinyl transferase (SFP Synthase or ACP Synthase).

    While ACP Synthase (NEB #P9301) will preferentially label the ACP-tag, SFP Synthase (NEB #P9302) will modify both ACP-tag and MCP-tag.

    Having no cysteines, the ACP-tag and the MCP-tag are particularly suited for specifically labeling cell-surface proteins, and should be useful for labeling secreted proteins with disulfide bridges such as antibodies.

    There are two steps to using this system: subcloning and expression of the protein of interest as an ACP-tag or MCP-tag fusion, and labeling of the fusion protein using the appropriate synthase with the CoA substrate of choice. Expression of ACP- and MCP-tagged proteins is described in the documentation supplied with the pACP-tag and pMCP-tag plasmids, respectively. The labeling of the fusion proteins with the CoA substrate is described below.

    Figure 1:  Live CHO-K1 cells transiently transfected with pACP-GPI
    Figure 1:  Live CHO-K1 cells transiently transfected with pACP-GPI
     Cells were labeled with CoA 488 (green) in the presence of SFP Synthase for 60 minutes.
    Figure 2:Excitation (dotted line) and emission spectra of CoA 488 coupled to ACP-tag in buffer at pH 7.4
    Figure 2:Excitation (dotted line) and emission spectra of CoA 488 coupled to ACP-tag in buffer at pH 7.4


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