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CFH / Complement Factor H Antibody (clone OX-24)

Mouse Monoclonal Antibody

     
  • IHC - CFH / Complement Factor H Antibody (clone OX-24) ALS12526
    Anti-Factor H antibody IHC of human liver.
    detail
  • SPECIFICATION
  • CITATIONS
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  • BACKGROUND
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB, IHC-P, E, IP, FC
Primary Accession P08603
Reactivity Human
Host Mouse
Clonality Monoclonal
Clone Names OX-24
Calculated MW 139kDa
Dilution IHC-P (20 µg/ml)
Additional Information
Gene ID 3075
Other Names Complement factor H, H factor 1, CFH, HF, HF1, HF2
Target/Specificity Purified anti-human factor H (beta 1H) (139 kD) monoclonal antibody clone OX-24 inhibits the binding of factor H to surface bound C3. This antibody recognizes the human serum complement protein factor H and a 43-49kD truncated form of factor H present at.
Reconstitution & Storage Store at 4°C for short term applications. For long term storage, aliquot and store at -20°C.
PrecautionsCFH / Complement Factor H Antibody (clone OX-24) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name CFH
Synonyms HF, HF1, HF2
Function Glycoprotein that plays an essential role in maintaining a well-balanced immune response by modulating complement activation. Acts as a soluble inhibitor of complement, where its binding to self markers such as glycan structures prevents complement activation and amplification on cell surfaces (PubMed:21285368, PubMed:25402769). Accelerates the decay of the complement alternative pathway (AP) C3 convertase C3bBb, thus preventing local formation of more C3b, the central player of the complement amplification loop (PubMed:19503104, PubMed:26700768). As a cofactor of the serine protease factor I, CFH also regulates proteolytic degradation of already-deposited C3b (PubMed:23332154, PubMed:18252712, PubMed:28671664). In addition, mediates several cellular responses through interaction with specific receptors. For example, interacts with CR3/ITGAM receptor and thereby mediates the adhesion of human neutrophils to different pathogens. In turn, these pathogens are phagocytosed and destroyed (PubMed:9558116, PubMed:20008295).
Cellular Location Secreted.
Tissue Location Expressed in the retinal pigment epithelium (at protein level) (PubMed:25136834). CFH is one of the most abundant complement components in blood where the liver is the major source of CFH protein in vivo. in addition, CFH is secreted by additional cell types including monocytes, fibroblasts, or endothelial cells (PubMed:6444659, PubMed:2968404, PubMed:2139673, PubMed:25136834)
Research Areas
Citations (0)
citation

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Background

Factor H functions as a cofactor in the inactivation of C3b by factor I and also increases the rate of dissociation of the C3bBb complex (C3 convertase) and the (C3b)NBB complex (C5 convertase) in the alternative complement pathway.

References

Ripoche J.,et al.Biochem. J. 249:593-602(1988).
Gregory S.G.,et al.Nature 441:315-321(2006).
Schulz T.F.,et al.Eur. J. Immunol. 16:1351-1355(1986).
Kristensen T.,et al.J. Immunol. 136:3407-3411(1986).
Estaller C.,et al.J. Immunol. 146:3190-3196(1991).

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$ 467.50
Cat# ALS12526
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