Factor I antibody [3R/8]
GTX41627
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
Product group Antibodies
ReactivityHuman
TargetCFI
Overview
- SupplierGeneTex
- Product NameFactor I antibody [3R/8]
- Delivery Days Customer9
- Antibody SpecificityThis antibody recognizes complement factor I. Clone 3R/8 blocks function of complement factor I.
- Application Supplier NoteELISA: 1/500-1/4,000. Neutralizing/Inhibition: . *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID3R/8
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID3426
- Target nameCFI
- Target descriptioncomplement factor I
- Target synonymsAHUS3; ARMD13; C3B/C4B inactivator; C3BINA; C3b-INA; C3b-inactivator; complement component I; complement control protein factor I; complement factor I; complement factor I heavy chain; FI; IF; KAF; Konglutinogen-activating factor; light chain of factor I
- HostMouse
- IsotypeIgG1
- Protein IDP05156
- Protein NameComplement factor I
- Scientific DescriptionThis gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene. [provided by RefSeq, Dec 2015]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203