Microbial or cell evacuation is the science of evacuating microbes and other cells. There are mainly two common protocols for evacuating bacterial cells or microbial cells. The bacteriophage E lysis gene-based protocol and the Sponge-Like-Protocol. From their names the first protocol uses the bacteriophage E lysis gene to produce the E lysis protein inside the Gram-negative bacteria causing pore in the cell. The second protocol uses subcritical concentrations of some selected active chemical compounds to evacuate any kind of cells turning them to empty cells. It is able to evacuate prokaryotic, eukaryotic and Archie cells. Viruses are also evacuated and, in some applications, deactivated using the H2O2 bio-critical concentration. The evacuation process is able to remove the cytoplasm of the evacuated cells. In case of virus evacuation, it can degrade their genetic material keep it unable to infect cells or replicate inside it. Also, it keeps the cells, or the virus envelop 3D structure in correct forms. It keeps the surface antigens safe and able to activate the immune system. The absence of the cytoplasm and its contents is important for many applications. They include microbial cell ghost preparation, RNA and DNA removal or isolation, drug delivery, disinfectants, and the like. There is a misunderstanding for the concept of the Sponge-Like-Protocol. There is a mix between the minimum inhibition concentration and the minimum growth concentration. This review will revise some of the tactics used for cell evocation. It will describe the Sponge-Like Protocol in more detail. Additionally, it concerns with summarizing the main concept of the Sponge-Like Protocol aiming to a successful cell/microbe/virus ghost's preparation with correct surface antigens.