This is largely tissue and target-dependent. This also depends on how your tissue has been prepared - paraffin embedded, snap frozen, etc.
In principle however, there are five main steps:
Fixation of the tissue if not already previously done during preparation
Permeabilisation using aldehydes or alcohols
Blocking
Primary and secondary staining
Visualisation (microscopy)
Between these you have some wash steps to complete and other various optimisations to perform. In some cases, you may also have to perform antibody retrieval (usually with paraffin embedded sections).
If you provide more details, I'm sure we can find an optimal protocol for you to use.
Hi, like Jack mentioned, it really depends on what type of tissue you have.
Is it formalin-fixed paraffin-embedded (FFPE) tissue, or is it frozen tissue (Fr) in OCT?
If it is FFPE-tissue, you need to de-paffinize it in order to start the staining.
If it is Fr-tissue, you just need to wash off OCT with TBST.
Then, your tissue is ready to start regular IHC, starting from blocking step. But there are different detection methods apply: FFPE-tissue with Chromogenic-IHC using DAB; and also can be done with Fluorescent 2dary detection. Fr-tissue, you can detect with Fluorescent 2dary too. Once you find out which tissue is yours (how it's prepared), then rest of the protocol perhaps you could find it online by searching either for FFPE- or Fr-tissues.