“…The methodology employed to obtain recombinant PAP2 is critical for this protein. Indeed, comparison with other commercially available forms of PAP2, where protein was subjected to ammonium chloride (NH 4 Cl) precipitation as part of the purification protocol, demonstrated that NH 4 Cl methodology completely abolished protein function in our macrophage stimulation assays [21]. It is clear that this protein family (Reg, PAP) requires particular handling and delicate purification methods to maintain optimal biological function.…”
These data demonstrate that both methods maintain functional immunomodulatory integrity for PAP2 and provide the ability to generate sufficient quantities to further study structure and function.
“…The methodology employed to obtain recombinant PAP2 is critical for this protein. Indeed, comparison with other commercially available forms of PAP2, where protein was subjected to ammonium chloride (NH 4 Cl) precipitation as part of the purification protocol, demonstrated that NH 4 Cl methodology completely abolished protein function in our macrophage stimulation assays [21]. It is clear that this protein family (Reg, PAP) requires particular handling and delicate purification methods to maintain optimal biological function.…”
These data demonstrate that both methods maintain functional immunomodulatory integrity for PAP2 and provide the ability to generate sufficient quantities to further study structure and function.
In older animals, there is depressed PAP expression related to a blunted inflammatory response in AP which is associated with worsened bacterial infiltration and higher C-reactive protein level; this may explain the more aggressive clinical course.
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