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C3, HUMAN

Base Information
  • Chemical Name:C3, HUMAN
  • CAS No.:80295-41-6
  • Molecular Formula:
  • Molecular Weight:0
  • Hs Code.:
C3, HUMAN

Synonyms:COMPLEMENT 3, HUMAN;COMPLEMENT C3, HUMAN;COMPLEMENT C3;C3, HUMAN;COMPLEMENT C3 FROM HUMAN SERUMFROZEN SOL UTION;complement c3 from human serum

Suppliers and Price of C3, HUMAN
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Complement C3, Human
  • 10x96Tests
  • $ 1117.00
  • Sigma-Aldrich
  • Complement C3 from human serum ≥3000?C3H50 units/mg (using C3 deficient serum)
  • 0.1 mg
  • $ 688.00
  • Sigma-Aldrich
  • Complement C3 from human serum ≥3000 C3H50 units/mg (using C3 deficient serum)
  • .1mg
  • $ 663.00
  • Sigma-Aldrich
  • Complement C3, Human
  • 250ug
  • $ 283.00
  • Sigma-Aldrich
  • Complement C3, Human Complement C3, Human, CAS 80295-41-6, is a native C3 component. Glycoprotein composed of two non-identical disulfide-bonded subunits of 115 kDa (α) and 75 kDa (β).
  • 250 μg
  • $ 271.95
Total 2 raw suppliers
Chemical Property of C3, HUMAN
Chemical Property:
  • Storage Temp.:−70°C 
Purity/Quality:

98%,99%, *data from raw suppliers

Complement C3, Human *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
MSDS Files:
Useful:
  • Uses Complement C3 is important in complement activation through the classical and alternative pathways. Complement C3 has been used in studies of bacterial defense against the complement system. Research on streptococcus infection has shown that Streptococcal pyrogenic exotoxin B (SPE B), a cysteine protease, can prevent phagocytic activity via cleavage of the C3 and impairing the pathways of the compliment system. C3 deficiency can result in recurrent infections and immune complex disorders. Recent research has shown that inherited C3 deficiency can occur either through homozygous mutations or through compound heterozygous mutations,
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