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Total coliform and E. coli analyses were performed using a chromogenic medium.
Total coliform and E. coli analyses were performed using a chromogenic medium (Colilert-IDEXX®; IDEXX Laboratories, Inc., ME, USA).
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Each lot of LPS was standardized for biologic activity using a chromogenic Limulus amebocyte lysate assay (GenScript, Piscataway, NJ, USA) to adjust for any variation between lots.
Endotoxin levels were measured during all purification steps (Supplementary Fig. 11b) using a chromogenic limulus amebocyte lysate (LAL) endotoxin assay kit (GenScript).
Xase and prothrombinase activity were assayed using a chromogenic substrate.
The bands were visualized using a chromogenic substrate for alkaline phosphatase.
Using a chromogenic assay, we assessed activity of PL in psoriasis.
Osteopontin (OPN) was detected by using a chromogenic substrate for the secondary antibody according to the kit manufacturer's instructions.
Elastase activity was thereafter measured using a chromogenic assay.
Anti-Xa levels were measured photometrically using a chromogenic technique (ACL top, Instrumentation Laboratory).
Antifactor Xa activity was determined using a chromogenic substrate (COACUTE®, Chromogenix AB, Mölndal, Sweden).
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