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M-CSF/CSF1 Kit ELISA

CSF1 Reactivité: Humain Colorimetric Sandwich ELISA 0.313-5 ng/mL Cell Culture Cells, Milk, Plasma, Serum
N° du produit ABIN5564632
  • Antigène Voir toutes M-CSF/CSF1 (CSF1) Kits ELISA
    M-CSF/CSF1 (CSF1) (Colony Stimulating Factor 1 (Macrophage) (CSF1))
    Reactivité
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    0.313-5 ng/mL
    Seuil minimal de détection
    0.313 ng/mL
    Application
    ELISA
    Fonction
    The AssayMax™ Human MCSF ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of human MCSF in plasma, milk, and cell culture samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures human MCSF in approximately 4 hours. A polyclonal antibody specific for human MCSF has been pre-coated onto a 96-well microplate with removable strips. MCSF in standards and samples is sandwiched by the immobilized antibody and a biotinylated polyclonal antibody specific for human MCSF, which is recognized by a streptavidin- peroxidase conjugate. All unbound material is 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
    Cell Culture Cells, Milk, Plasma, Serum
    Analytical Method
    Quantitative
    Ingrédients
    Human MCSF Microplate: A 96-well polystyrene microplate (12 strips of 8 wells) coated with a polyclonal antibody against human MCSF. Sealing Tapes: Each kit contains 3 precut, pressure sensitive sealing tapes that can be cut to fit the format of the individual assay. Human MCSF Standard: Human MCSF in a buffered protein base (5 ng, lyophilized, 2 vials). Biotinylated Human MCSF Antibody (50x): A 50-fold concentrated biotinylated polyclonal antibody against human MCSF (120 l). MIX Diluent Concentrate (10x): A 10-fold concentrated buffered protein base (30 ml). Standard Diluent (1x): A buffered protein base with stabilizer (2 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 l). Chromogen Substrate: A ready-to-use stabilized peroxidase chromogen substrate tetramethylbenzidine (8 ml). Stop Solution: A 0.5 N hydrochloric acid solution to stop the chromogen substrate reaction (12 ml).
    Matériel non inclus
    Microplate reader capable of measuring absorbance at 405 nm. Pipettes (1-20 µL, 20-200 µL, and multiple channel). Deionized or distilled reagent grade water Incubator (37 °C)
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  • Durée du test
    3 h
    Plaque
    Pre-coated
    Protocole
    • Step 1. Add 50 μL of Standard or Sample per well. Incubate 2 hours.
    • Step 2. Wash, then add 50 μL of Biotinylated Antibody per well. Incubate 1 hour.
    • Step 3. Wash, then add 50 μL of SP Conjugate per well. Incubate 30 minutes.
    • Step 4. Wash, then add 50 μL of Chromogen Substrate per well. Incubate 25 minutes.
    • Step 5. 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. MIX Diluent Concentrate (10x): If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. Dilute the MIX Diluent Concentrate 10-fold with reagent grade water. Store for up to 30 days at 2-8 °C. Human MCSF Standard: Reconstitute the Human MCSF Standard (5 ng) with 0.5 mL of Standard Diluent to generate a 10 ng/mL standard stock solution. Allow the standard to sit for 10 minutes with gentle agitation prior to making dilutions. Prepare duplicate or triplicate standard points by serially diluting from the standard stock solution (10 ng/mL) 2-fold with MIX Diluent to produce 5, 2.5, 1.25, 0.625, and 0.313 ng/mL solutions. MIX Diluent serves as the zero standard (0 ng/mL). Aliquot remaining stock solution to limit repeated freeze-thaw cycles. This solution should be stored at -20 °C and used within 48 hours. 4 Standard Point Dilution [MCSF] (ng/mL) P1 1 part Standard (10 ng/mL) + 1 part MIX Diluent 5.0 P2 1 part P1 + 1 part MIX Diluent 2.5 P3 1 part P2 + 1 part MIX Diluent 1.25 P4 1 part P3 + 1 part MIX Diluent 0.625 P5 1 part P4 + 1 part MIX Diluent 0.313 P6 MIX Diluent 0.0 Biotinylated Human MCSF Antibody (50x): Spin down the antibody briefly and dilute the desired amount of the antibody 50-fold with MIX Diluent. The undiluted antibody should be stored 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 20-fold with reagent grade water. SP Conjugate (100x): Spin down the SP Conjugate briefly and dilute the desired amount of the conjugate 100-fold with MIX Diluent. The undiluted conjugate should be stored at -20 °C.

    Prélèvement de l'échantillon
    Plasma: Collect plasma using one-tenth volume of 0.1 M sodium citrate as an anticoagulant. Centrifuge samples at 3000 x g for 10 minutes and collect plasma. The sample is suggested for use at 1x, however, user should determine optimal dilution factor depending on application needs. The undiluted samples can be stored at -20 °C or below for up to 3 months. Avoid repeated freeze-thaw cycles (EDTA or Heparin can also be used as an anticoagulant). Milk: Collect milk using sample tube. Centrifuge samples at 800 x g for 10 minutes. A 10-fold sample dilution is suggested into MIX Diluent, however, user should determine optimal dilution factor depending on application needs. The undiluted samples can be stored at -20 °C or below for up to 3 months. Avoid repeated freeze-thaw cycles. Cell Culture Supernatants: Centrifuge cell culture media at 3000 x g for 10 minutes at 4 °C to remove debris and collect supernatants. Samples can be stored at -20 °C or below. Avoid repeated freeze-thaw cycles.
    Procédure de l'essai

    Prepare all reagents, standard solutions, and samples as instructed. Bring all reagents to room temperature before use. The assay is performed at room temperature (20-25 °C). 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 l of Human MCSF Standard or sample to each well. Gently tap plate to thoroughly coat the wells. Break any bubbles that may have formed. Cover wells with a sealing tape and incubate for 2 hours. Start the timer after the last addition. Wash five times with 200 l 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 l 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 l of Biotinylated Human MCSF Antibody to each well. Gently tap plate to thoroughly coat the wells. Break any bubbles that may have formed. Cover wells with a sealing tape and incubate for 1 hour. Wash the microplate as described above. Add 50 l of Streptavidin-Peroxidase Conjugate to each well. Gently tap plate to thoroughly coat the wells. Break any bubbles that may have 5 formed. Cover wells with a sealing tape 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 l of Chromogen Substrate to each well. Gently tap plate to thoroughly coat the wells. Break any bubbles that may have formed. Incubate for 25 minutes or until the optimal blue color density develops. Add 50 l of Stop Solution to each well. The color will change from blue to yellow. Gently tap plate to ensure thorough mixing. Break any bubbles that may have formed. 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 (OD) 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.
    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    This product is for Research Use Only and is not intended for use in diagnostic procedures. Prepare all reagents (diluent buffer, wash buffer, standard, biotinylated antibody, and SP conjugate) as instructed, prior to running the assay. 2 Prepare all samples prior to running the assay. The dilution factors for the samples are suggested in this insert. 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 Stop Solution is an acidic solution. The kit should not be used beyond the expiration date.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Upon arrival, immediately store components of the kit at recommended temperatures up to the expiration date. Store Standard, SP Conjugate, and Biotinylated Antibody at -20°C. Store Microplate, Diluent Concentrate (10x), Standard Diluent (1x), 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 30 days in a vacuum desiccator. 3
  • Antigène Voir toutes M-CSF/CSF1 (CSF1) Kits ELISA
    M-CSF/CSF1 (CSF1) (Colony Stimulating Factor 1 (Macrophage) (CSF1))
    Autre désignation
    Macrophage Colony Stimulating Factor (MCSF) (CSF1 Produits)
    Synonymes
    CSF-1 Kit ELISA, MCSF Kit ELISA, C87615 Kit ELISA, Csfm Kit ELISA, op Kit ELISA, csf1-1 Kit ELISA, zgc:172186 Kit ELISA, CSF1 Kit ELISA, csf1-2 Kit ELISA, zgc:158436 Kit ELISA, colony stimulating factor 1 Kit ELISA, colony stimulating factor 1 (macrophage) Kit ELISA, colony stimulating factor 1a (macrophage) Kit ELISA, macrophage colony-stimulating factor 1 Kit ELISA, macrophage colony stimulating factor Kit ELISA, colony stimulating factor 1b (macrophage) Kit ELISA, CSF1 Kit ELISA, Csf1 Kit ELISA, csf1a Kit ELISA, LOC396599 Kit ELISA, LOC100860895 Kit ELISA, csf1b Kit ELISA
    Sujet
    Macrophage colony stimulating factor (MCSF), also known as lanimostim, CSF- 1 and M-CSF, is a 554-amino acid glycosylated polypeptide homodimer cytokine. MCSF is synthesized as an integral transmembrane glycoprotein that is assembled into disulfide-linked dimmers and rapidly underwent proteolytic cleavage to generate different soluble growth factor forms (1). One high molecular weight soluble form is a chondroitin sulfate proteoglycan (2). MCSF regulates survival, proliferation, and differentiation of hematopoietic precursor cells, especially mononuclear phagocytes such as macrophages and monocytes. It promotes the release of proinflammatory chemokines. MCSF also plays an important role in innate immunity and in inflammatory processes. It modulates osteoclast proliferation and differentiation, bone resorption, and normal bone development (3).
    ID gène
    1435
    UniProt
    P09603
    Pathways
    Signalisation RTK
Support technique