catalog number :
MBS245037
products full name :
Mouse Monoclonal [clone OX-21] (IgG1) to Human CFI / Complement Factor I
products short name :
CFI / Complement Factor I
products name syn :
Anti-CFI / Complement Factor I Antibody (clone OX-21) IHC-plus; CFI; AHUS3; C3BINA; C3b-inactivator; C3B/C4B inactivator; Complement component I; Complement component factor i; Factor I; FI; KAF; I factor; I factor (complement); C3b-INA; Complement factor I; Light chain of factor I; Human CFI; Complement Factor I
other names :
complement factor I preproprotein; Complement factor I; complement factor I; C3b-inactivator; C3B/C4B inactivator; complement component I; light chain of factor I; Konglutinogen-activating factor; complement factor I heavy chain; complement control protein factor I; complement factor I; C3B/C4B inactivatorCleaved into the following 2 chains:Complement factor I heavy chain; Complement factor I light chain
other gene names :
CFI; CFI; FI; IF; KAF; AHUS3; ARMD13; C3BINA; C3b-INA; IF
uniprot entry name :
CFAI_HUMAN
specificity :
Purified human Complement Factor 1
purity :
Protein G Purified
form :
PBS, 0.02% sodium azide. Sourced in Ascites.
storage stability :
Store at 4 degree C for short term applications. For long term storage, aliquot and store at -20 degree C.
tested application :
Immunohistochemistry (IHC - Paraffin), Western Blot (WB), Immunoprecipitation (IP), Flow Cytometry (FC/FACS), ELISA (EIA)
app notes :
ELISA, Flo, IHC-P (20 ug/ml), IP, WB. Usage: Immunohistochemistry: was validated for use in immunohistochemistry on a panel of 21 formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with the primary anti.
other info1 :
Target Species: Human. Immunogen Description: Human complement factor I
other info2 :
Immunogen Type: Purified protein
products categories :
Family: Protease. Subfamily: Serine S1
ncbi acc num :
NP_000195.2
ncbi gb acc num :
NM_000204.3
ncbi mol weight :
65,750 Da
ncbi pathways :
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!!Regulation Of Complement Cascade Pathway 576254!!Staphylococcus Aureus Infection Pathway 172846!!Staphylococcus Aureus Infection Pathway 171867
ncbi summary :
This 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 uraemic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immmune deposits is another condition associated with mutation of this gene. [provided by RefSeq, Jul 2008]