catalog number :
MBS9125401
products short name :
[C9]
products name syn :
[ARMD15, C9D]
other names :
[Complement component C9; Complement component C9; complement component C9; complement component 9]
products gene name :
[C9]
other gene names :
[C9; C9; C9D; ARMD15]
uniprot entry name :
CO9_HUMAN
reactivity :
Human, Mouse
purity :
Affinity purification
storage stability :
Store at -20°C. Avoid freeze/thaw cycles.
tested application :
Western Blot (WB)
app notes :
1:500- 1:2000
image1 heading :
Western Blot (WB)
other info1 :
Source: Rabbit. Immunogen: Recombinant funsion protein containing a sequence corresponding to amino acids 22-265 of human C9 (NP_001728.1). Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH 7.3. Calculated MW: 63 kDa. Observed MW: 70 kDa
products categories :
Polyclonal
products description :
This gene encodes the final component of the complement system. It participates in the formation of the Membrane Attack Complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in this gene cause component C9 deficiency.
ncbi pathways :
Amoebiasis Pathway (167324); Amoebiasis Pathway (167191); Complement Activation, Classical Pathway (198823); Complement And Coagulation Cascades Pathway (198880); Complement And Coagulation Cascades Pathway (83073); Complement And Coagulation Cascades Pathway (484); Complement Cascade Pathway (106405); Immune System Pathway (106386); Innate Immune System Pathway (106387); Prion Diseases Pathway (101144)
ncbi summary :
This gene encodes the final component of the complement system. It participates in the formation of the Membrane Attack Complex (MAC). The MAC assembles on bacterial membranes to form a pore, permitting disruption of bacterial membrane organization. Mutations in this gene cause component C9 deficiency. [provided by RefSeq, Feb 2009]
uniprot summary :
C9: Constituent of the membrane attack complex (MAC) that plays a key role in the innate and adaptive immune response by forming pores in the plasma membrane of target cells. C9 is the pore-forming subunit of the MAC. Defects in C9 are a cause of complement component 9 deficiency (C9D). A rare defect of the complement classical pathway associated with susceptibility to severe recurrent infections, predominantly by Neisseria gonorrhoeae or Neisseria meningitidis. Belongs to the complement C6/C7/C8/C9 family. Protein type: Extracellular matrix; Membrane protein, multi-pass; Membrane protein, integral; Apoptosis. Chromosomal Location of Human Ortholog: 5p14-p12. Cellular Component: membrane attack complex; integral to plasma membrane; cytoplasm; plasma membrane; extracellular region. Biological Process: complement activation, alternative pathway; regulation of complement activation; innate immune response; hemolysis by symbiont of host red blood cells; complement activation, classical pathway. Disease: Macular Degeneration, Age-related, 15; Complement Component 9 Deficiency