MBL Pathway of Complement Analysis Protocol

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The activation of the complement-activated mannan-binding lectin (MBL) pathway is similar to the classical pathway (CP). MBL recognizes and interacts with the mannose residues on the pathogenic microorganisms and undergoes conformational changes, then activates downstream serine proteases with similar biological activities and functions to C1s, MASP-1 and MASP-2. MASP-2 hydrolyzes C4 and C2 molecules, while MASP-1 directly cut C3, and then forms C3 convertase. The MBL pathway exerts complement functions by activating the same membrane attack unit as the CP. The lectin pathway provides another antibody-independent way to stimulate the complement system. Here, we briefly describe the experimental procedures for detecting the complement function of the MBL pathway in samples to provide technical references for your experimental project.

MBL Pathway of Complement Analysis Protocol

The novel method to verify the function of the MBL pathway is carried out by ELISA theory.

Workflow of MBL pathway of complement analysis protocol. (Creative Biolabs Original) Fig 1. Workflow of MBL pathway of complement analysis protocol.

Time-Resolved Immunofluorescence Assay For Mbl Function Test Protocol.

Time-resolved immunofluorescence assays were also used to determine the ability of serum or plasma samples to mediate activation of complement factor C4 via the MBL pathway of complement.

Workflow of time-resolved immunofluorescence assay protocol. (Creative Biolabs Original) Fig 2. Workflow of time-resolved immunofluorescence assay protocol. (Creative Biolabs)

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