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They are not regulated under FDA drug manufacturing standards

Every time a needle punctures the rubber stopper, there's a minuscule risk of introducing contaminants

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Support team responded to a pre-order question within 2 hours. The TFA residue data on the COA was the deciding factor for us our cell assay protocols are sensitive to TFA contamination

However, in certain viral infections, antibodies intended to protect the host can instead drive pathogenic processes through mechanisms like ADE and the induction of autoimmunity [7,8,9,33,34,35]