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Complement Factor H Kit ELISA

CFH Reactivité: Humain Colorimetric Sandwich ELISA Cell Culture Supernatant, Milk, Plasma, Saliva, Serum, Urine
N° du produit ABIN1440238
  • Antigène Voir toutes Complement Factor H (CFH) Kits ELISA
    Complement Factor H (CFH)
    Reactivité
    • 8
    • 7
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Seuil minimal de détection
    ~ 0.2 ng/mL
    Application
    ELISA
    Fonction
    The AssayMax Human Complement Factor H (FH) ELISA kit is designed for detection of human FH in urine, saliva, milk, plasma, serum and cell culture samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures FH in less than 4 hours. An antibody specific for FH has been pre-coated onto a 96-well microplate with removable strips. Human FH in standards and samples is sandwiched by the immobilized antibody and the biotinylated polyclonal antibody specific for human FH, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.
    Marque
    AssayMax
    Type d'échantillon
    Serum, Milk, Saliva, Urine, Plasma, Cell Culture Supernatant
    Analytical Method
    Quantitative
    Réactivité croisée (Details)
    Cross-Reactivity: Monkey 20%
    10% FBS in culture media will not affect the assay.
    Attributs du produit
    Standard Added Value: 0.5 - 5 ng/mL
    Ingrédients
    Complement Factor H Microplate: A 96-well polystyrene microplate (12 strips of 8 wells) coated with a polyclonal antibody against human FH.
    Sealing Tapes: Each kit contains 3 precut, pressure sensitive sealing tapes that can be cut to fit the format of the individual assay.
    Complement Factor H Standard: Human FH in a buffered protein base (144 ng, lyophilized).
    Biotinylated Complement Factor H Antibody (50x): A 50-fold concentrated biotinylated polyclonal antibody against human FH (140 µL).
    EIA Diluent Concentrate (10x): A 10-fold concentrated buffered protein base (30 mL).
    Wash Buffer Concentrate (20x): A 20-fold concentrated buffered surfactant (30 mL, 2 bottles).
    Streptavidin-Peroxidase Conjugate (SP Conjugate): A 100-fold concentrate (80 µL).
    Chromogen Substrate: A ready-to-use stabilized peroxidase chromogen substrate tetramethylbenzidine (8 mL).
    Stop Solution: A 0.5 N hydrochloric acid to stop the chromogen substrate reaction (12 mL).
    Matériel non inclus
    Microplate reader capable of measuring absorbance at 450 nm.
    Pipettes (1-20 µL, 20-200 µL, 200-1000 µL and multiple channel).
    Deionized or distilled reagent grade water.
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  • Volume d'échantillon
    50 μL
    Durée du test
    < 4 h
    Plaque
    Pre-coated
    Protocole
    Add 50 µL of standard/samples per well. Incubate 2 hours. Wash, then add 50 µL of biotinylated antibody per well. Incubate 1 hour. Wash, then add 50 µL of SP per well. Incubate 30 minutes. Wash, then add 50 µL of Chromogen Substrate per well. Incubate 20 minutes. Add 50 µL of Stop Solution per well. Read at 450 nm immediately.
    Préparation des réactifs

    Freshly dilute all reagents and bring all reagents to room temperature before use.
    EIA Diluent Concentrate (10x): If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. Dilute the EIA Diluent 1:10 with reagent grade water. Store for up to 1 month at 2-8°C.
    Standard Curve: Reconstitute the 144 ng of Complement Factor H Standard with 4 mL of EIA Diluent to generate a stock solution of 36 ng/mL. Allow the standard to sit for 10 minutes with gentle agitation prior to making dilutions. Prepare duplicate or triplicate standard points by serially diluting the stock solution (36 ng/mL) 1:2 with equal volume of EIA Diluent to produce 18, 9, 4.5, 2.25, 1.125, 0.563, and 0.281 ng/mL. EIA Diluent serves as the zero standard (0 ng/mL). Any remaining solution should be frozen at -20°C and used within 30 days.
    Biotinylated Complement Factor H Antibody (50x): Spin down the antibody briefly and dilute the desired amount of the antibody 1:50 with EIA Diluent. Any remaining solution should be frozen at -20°C.
    Wash Buffer Concentrate (20x): If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. Dilute the Wash Buffer Concentrate 1:20 with reagent grade water.
    SP Conjugate (100x): Spin down the SP Conjugate briefly and dilute the desired amount of the conjugate 1:100 with EIA Diluent. Any remaining solution should be frozen at -20°C.

    Préparation de l'échantillon

    Plasma: Collect plasma using one-tenth volume of 0.1 M sodium citrate as an anticoagulant. Centrifuge samples at 2000 x g for 10 minutes and use supernatants. Dilute samples 1:200000 with EIA Diluent and assay. The undiluted samples can be stored at -20°C or below for up to 90 days. Avoid repeated freeze-thaw cycles. (EDTA or Heparin can also be used as an anticoagulant.)
    Serum: Samples should be collected into a serum separator tube. After clot formation, centrifuge samples at 2000 x g for 10 minutes. Remove serum. Dilute samples 1:200000 into EIA Diluent and assay. The undiluted samples can be stored at -20°C or below for up to 90 days. Avoid repeated freeze-thaw cycles.
    Cell Culture Supernatants: Collect cell culture media and centrifuge at 2000 x g for 10 minutes at 4°C to remove debris. The samples can be stored at -20°C or below. Avoid repeated freeze-thaw cycles.
    Saliva: Collect saliva using sample tube. Centrifuge samples at 800 x g for 10 minutes. Dilute saliva samples 1:50 into EIA Diluent and assay. The undiluted samples can be stored at -20°C or below for up to 3 months. Avoid repeated freeze-thaw cycles.
    Urine: Collect urine using sample pot. Centrifuge samples at 600 x g for 10 minutes. Dilute urine samples 1:10 into EIA Diluent and assay. The undiluted samples can be stored at -20°C or below for up to 3 months. Avoid repeated freeze-thaw cycles.
    Milk: Collect milk using sample tube. Centrifuge samples at 800 x g for 10 minutes. Dilute milk samples 1:200 into EIA Diluent and assay. The undiluted samples can be stored at -20°C or below for up to 3 months. Avoid repeated freeze-thaw cycles.

    Procédure de l'essai

    Prepare all reagents, working standards and samples as instructed.
    Remove excess microplate strips from the plate frame and return them immediately to the foil pouch with desiccants inside. Reseal the pouch securely to minimize exposure to water vapor and store in a vacuum desiccator.
    Add 50 µL of standard or sample per well. Cover wells with a sealing tape and incubate for 2 hours. Start the timer after the last sample addition.
    Wash five times with 200 µL of Wash Buffer manually. Invert the plate each time and decant the contents, hit 4-5 times on absorbent material to completely remove the liquid. If using a machine, wash six times with 300 µL of Wash Buffer and then invert the plate, decanting the contents, hit 4-5 times on absorbent material to completely remove the liquid.
    Add 50 µL of Biotinylated Complement Factor H Antibody to each well and incubate for 1 hour.
    Wash the microplate as described above.
    Add 50 µL of Streptavidin-Peroxidase Conjugate per well and incubate for 30 minutes. Turn on the microplate reader and set up the program in advance.
    Wash the microplate as described above.
    Add 50 µL of Chromogen Substrate per well and incubate for approximately 20 minutes or till the optimal blue color density develop. Gently tap the plate to ensure thorough mixing and break the bubbles in the well with pipette tip.
    Add 50 µL of Stop Solution to each well. The color will change from blue to yellow.
    Read the absorbance on a microplate reader at a wavelength of 450 nm immediately. If wavelength correction is available, subtract readings at 570 nm from those at 450 nm to correct optical imperfections. Otherwise, read the plate at 450 nm only. Please note that some unstable black particles may be generated at high concentration points after stopping the reaction for about 10 minutes, which will reduce the readings.

    Calcul des résultats

    Calculate the mean value of the duplicate or triplicate readings for each standard and sample.
    To generate a standard curve, plot the graph using the standard concentrations on the x-axis and the corresponding mean 450 nm absorbance on the y-axis. The best-fit line can be determined by regression analysis using log-log or four-parameter logistic curve-fit.
    Determine the unknown sample concentration from the Standard Curve and multiply the value by the dilution factor.

    Précision du teste
    Intra-assay and inter-assay coefficients of variation were 5.0 % and 7.2 % respectively.
    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    Prepare all reagents (working diluent buffer, wash buffer, standards, biotinylated antibody, and SP conjugate) as instructed, prior to running the assay.
    Prepare all samples prior to running the assay. The dilution factors for the samples are suggested in this protocol. However, the user should determine the optimal dilution factor.
    Spin down the SP conjugate vial and the biotinylated antibody vial before opening and using contents.
    The kit should not be used beyond the expiration date.
    The Stop Solution is an acidic solution.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store components of the kit at 2-8°C or -20°C upon arrival up to the expiration date.
    Store SP Conjugate and biotinylated antibody at -20°C.
    Store Microplate, Diluent Concentrate (10x), Wash Buffer, Stop Solution, and Chromogen Substrate at 2-8°C.
    Unused microplate wells may be returned to the foil pouch with the desiccant packs and resealed. May be stored for up to 1 month in a vacuum desiccator.
    Diluent (1x) may be stored for up to 1 month at 2-8°C.
    Store standard at 2-8°C before reconstituting with diluent and at -20°C after reconstituting with diluent. 3
  • Antigène Voir toutes Complement Factor H (CFH) Kits ELISA
    Complement Factor H (CFH)
    Autre désignation
    Complement Factor H (CFH Produits)
    Synonymes
    AHUS1 Kit ELISA, AMBP1 Kit ELISA, ARMD4 Kit ELISA, ARMS1 Kit ELISA, CFHL3 Kit ELISA, FH Kit ELISA, FHL1 Kit ELISA, HF Kit ELISA, HF1 Kit ELISA, HF2 Kit ELISA, HUS Kit ELISA, Mud-1 Kit ELISA, NOM Kit ELISA, Sas-1 Kit ELISA, Sas1 Kit ELISA, Fh Kit ELISA, CFH Kit ELISA, im:7147412 Kit ELISA, si:ch211-207o17.2 Kit ELISA, fH Kit ELISA, armd4 Kit ELISA, arms1 Kit ELISA, cfh Kit ELISA, cfhl3 Kit ELISA, fhl1 Kit ELISA, hf1 Kit ELISA, hf2 Kit ELISA, hus Kit ELISA, complement factor H Kit ELISA, complement component factor h Kit ELISA, complement factor H-related protein 5 Kit ELISA, complement factor H L homeolog Kit ELISA, CFH Kit ELISA, Cfh Kit ELISA, cfh Kit ELISA, LOC100399888 Kit ELISA, LOC100733902 Kit ELISA, cfh.L Kit ELISA
    Sujet
    Complement Factor H (FH) is a 1,213-residue plasma glycoprotein that regulates the function of the alternative complement pathway. The FH gene encodes a 155-kDa protein containing 20 tandem complement control protein (CCPs) modules (also known as short consensus repeats) with about 60 amino acids each, and an alternative spliced 45-kDa protein. It binds to C3b to accelerate the decay of the C3 convertase C3bBb, and also acts as a cofactor for complement factor I- mediated C3b cleavage. Human FH is particularly important for selectively protecting self-surfaces by binding to glycosaminoglycans on host cells. Mutations and polymorphisms in FH have been linked to atypical hemolytic uremic syndrome, membranoproliferative glomerulonephritis, and age-related macular degeneration.
    Pathways
    Système du Complément, Cellular Response to Molecule of Bacterial Origin
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