Human Complement C5
Native, whole molecule
Produktdetails
Synonyms
C5
Description of Human Complement C5
Complement C5, a glycoprotein composed of α (115 kDa) and β (75 kDa) chains, serves as the linchpin of complement-mediated immunity. Cleaved by C5 convertases into C5a (potent anaphylatoxin) and C5b (initiator of membrane attack complex/MAC), it bridges inflammatory signaling and pathogen lysis. C5a drives chemotaxis, leukocyte activation, and vascular permeability via C5aR1/C5aR2 receptors, while C5b-9 (MAC) induces microbial cytolysis. C5 deficiency increases susceptibility to recurrent pyogenic infections (e.g., Neisseria) and Leiner’s disease. Elevated C5a correlates with rheumatoid arthritis, Guillain-Barré syndrome, and chemotherapy-induced neuropathy.
Source
Human plasma non-reactive for HBsAG, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA approved tests
Storage
For long term, store Human Complement C5 at ≤ -80°C.
Applications
Inflammation, Infection, Autoimmune Diseases, Myasthenia Gravis, Age Related Macular Degeneration.
Citations/Publications
NCBI: https://www.ncbi.nlm.nih.gov/protein/P01031/
Shipped with dry ice
Gel Scan of Human Complement C5
Fig. 1: SDS-PAGE Gel |
Usage: For research use only. Not for use in diagnostic or therapeutic procedures. Not for human use.
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Payment Methods
Paying by bank transfer
