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Details for Product KITLG ELISA Kit No. ABIN612747, Supplier: Log in to see
  • 710-712
  • blz
  • Clo
  • Con
  • contrasted
  • CSF
  • FPH2
  • Gb
  • Kitl
  • kitl
  • KITL
  • Kitlg
  • KL-1
  • kl-1
  • Mgf
  • MGF
  • mgf
  • scf
  • SCF
  • SF
  • SHEP7
  • Sl
  • SLF
  • steel
  • Xkl-1
  • Xsl
  • Xsl-1
  • Xsl-2
Mouse (Murine) KIT Ligand ELISA Kit
Mouse (Murine)
Kits with alternative reactivity to:
Methode Type
Sandwich ELISA
Minimum Detection Limit
0.06 ng/mL
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Purpose The AssayMax Mouse SCF ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of mouse SCF in cell culture supernatant
Sample Type Cell Culture Supernatant
Detection Method Colorimetric
Components Mouse SCF Microplate: A 96-well polystyrene microplate (12 strips of 8 wells) coated with a polyclonal antibody against mouse SCF. Sealing Tapes: Each kit contains 3 pre-cut, pressure-sensitive sealing tapes that can be cut to fit the format of the individual assay. Mouse SCF Standard: Mouse SCF in a buffered protein base (4 ng, lyophilized). Biotinylated SCF Antibody (50x): A 50-fold concentrated biotinylated polyclonal antibody against SCF (140µl). MIx 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 (80µl). 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).
Material not included Microplate reader capable of measuring absorbance at 450 nm. Pipettes (1-20 µL, 20-200 µL, 200-1000µLand multiple channel). Deionized or distilled reagent grade water
Alternative Name Stem Cell Factor (SCF) (KITLG ELISA Kit Abstract)
Background Stem Cell Factor (SCF) is known as c-Kit receptor ligand, KL, steel factor, or mast cell growth factor and is expressed in fibroblasts, thymus tissue, spleen, testes, placenta and mast cells. SCF is a cytokine that exists in two forms produced by alternative splicing: a soluble form of approximately 31 kDa and a membrane-bound form of approximately 32 kDa, lacking the proteolytic site for processing into the soluble form (1-4). SCF not only plays an important role in hematopoiesis, reproduction, melanogenesis and tumor progression, but also involved in proliferation and differentiation of mast cells. It stimulates mast cell activation in human bronchi and induces smooth muscle cell contraction. Both increased expression of SCF and its receptor c-Kit were found in asthma patients. During chronic stroke, SCF in combination with granulocyte-colony stimulating factor (G-CSF) treatment can enhance repair of brain damage. Blocking SCF-c-kit signaling is sufficient to inhibit lung cancer stem cell proliferation and survival promoted by chemotherapy.
Research Area Cell/Tissue Markers
Pathways RTK Signaling, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway
Sample Volume 50 μL
Assay Time < 4 h
Plate Pre-coated,Strips (12 x 8)
Protocol This assay employs a quantitative sandwich enzyme immunoassay technique that measures mouse SCF in less than 4 hours. A polyclonal antibody specific for mouse SCF has been pre-coated onto a 96-well microplate with removable strips. SCF in standards and samples is sandwiched by the immobilized antibody and the biotinylated polyclonal antibody specific for SCF, 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.
Reagent Preparation

Freshly dilute all reagents and bring all reagents to room temperature before use. If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved. MIx Diluent Concentrate (10x): Dilute the MIx Diluent 1:10 with reagent grade water. Store for up to 1 month at 2-8°C. Standard Curve: Reconstitute the 4 ng of SCF Standard with 1 ml of MIx Diluent to generate a standard solution of 4 ng/ml. Allow the standard to sit for 10 minutes with gentle 2 agitation prior to making dilutions. Prepare duplicate or triplicate standard points by serially diluting the standard solution (4 ng/ml) 1:2 with MIx Diluent to produce 2, 1, 0.5, 0.25, 0.125, and 0.0625 ng/ml solutions. MIx Diluent serves as the zero standard (0 ng/ml). Any remaining solution should be frozen at -20°C. Standard Point Dilution [SCF] (ng/ml) P1 Standard Stock (4 ng/ml) 4.000 P2 1 part P1 + 1 part MIx Diluent 2.000 P3 1 part P2 + 1 part MIx Diluent 1.000 P4 1 part P3 + 1 part MIx Diluent 0.500 P5 1 part P4 + 1 part MIx Diluent 0.250 P6 1 part P5 + 1 part MIx Diluent 0.125 P7 1 part P6 + 1 part MIx Diluent 0.063 P8 MIx Diluent 0.000 Biotin SCF Antibody (50x): Spin down the antibody briefly and dilute the desired amount of the antibody 1:50 with MIx Diluent. Any remaining solution should be frozen at -20°C. Wash Buffer Concentrate (20x): 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 MIx Diluent. Any remaining solution should be frozen at -20°C.

Sample Collection Cell Culture Supernatants: Centrifuge cell culture media at 3000 x g for 10 minutes to remove debris. Collect supernatants and assay. Store samples at -20°C or below. Avoid repeated freeze-thaw cycles.
Assay Procedure

Prepare all reagents, working standards and samples as instructed. Bring all reagents to room temperature before use. The assay is performed at room temperature (20 - 30 °C). Remove excess microplate strips from the plate frame and return them immediately to the foil pouch with desiccant inside. Reseal the pouch securely to minimize exposure to water vapor and store in a vacuum desiccator. Add 50 µL of SCF standard or sample per well. Cover wells with a sealing tape and incubate for two 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 it 4-5 times on absorbent paper towel to completely remove the liquid. If using a machine wash six times with 300 µL of Wash Buffer and then invert the plate, decant the contents, hit it 4-5 times on absorbent paper towel to completely remove the liquid. Add 50 µL of Biotinylated SCF Antibody to each well and incubate for one hour. Wash the microplate as described above. Add 50 µL of Streptavidin-Peroxidase Conjugate to each 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 about 15 minutes or till the optimal blue color density develops. Gently tap 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 3 unstable black particles may be generated at high concentration points after stopping the reaction for about 10 minutes, which will reduce the readings.

Calculation of Results

Calculate the mean value of the 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. Standard Curve The curve is provided for illustration only. A standard curve should be generated each time the assay is performed.

Assay Precision Intra-assay and inter-assay coefficients of variation were 4.5% and 7.2% respectively.
Restrictions For Research Use only
Handling Advice 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.
Storage 4 °C/-20 °C
Storage Comment 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 Opened unused microplate wells may be returned to the foil pouch with the desiccant packs. Reseal along zip-seal. 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.
Background publications Levina, Marrangoni, Wang, Parikh, Su, Herberman, Lokshin, Gorelik: "Elimination of human lung cancer stem cells through targeting of the stem cell factor-c-kit autocrine signaling loop." in: Cancer research, Vol. 70, Issue 1, pp. 338-46, 2010 (PubMed).

Piao, Gonzalez-Toledo, Xue, Duan, Terao, Granger, Kelley, Zhao: "The role of stem cell factor and granulocyte-colony stimulating factor in brain repair during chronic stroke." in: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, Vol. 29, Issue 4, pp. 759-70, 2009 (PubMed).

Al-Muhsen, Shablovsky, Olivenstein, Mazer, Hamid: "The expression of stem cell factor and c-kit receptor in human asthmatic airways." in: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, Vol. 34, Issue 6, pp. 911-6, 2004 (PubMed).

Undem, Lichtenstein, Hubbard, Meeker, Ellis: "Recombinant stem cell factor-induced mast cell activation and smooth muscle contraction in human bronchi." in: American journal of respiratory cell and molecular biology, Vol. 11, Issue 6, pp. 646-50, 1994 (PubMed).

Brannan, Lyman, Williams, Eisenman, Anderson, Cosman, Bedell, Jenkins, Copeland: "Steel-Dickie mutation encodes a c-kit ligand lacking transmembrane and cytoplasmic domains." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 88, Issue 11, pp. 4671-4, 1991 (PubMed).

Flanagan, Leder: "The kit ligand: a cell surface molecule altered in steel mutant fibroblasts." in: Cell, Vol. 63, Issue 1, pp. 185-94, 1990 (PubMed).

Williams, Eisenman, Baird, Rauch, Van Ness, March, Park, Martin, Mochizuki, Boswell: "Identification of a ligand for the c-kit proto-oncogene." in: Cell, Vol. 63, Issue 1, pp. 167-74, 1990 (PubMed).

Zsebo, Williams, Geissler, Broudy, Martin, Atkins, Hsu, Birkett, Okino, Murdock: "Stem cell factor is encoded at the Sl locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor." in: Cell, Vol. 63, Issue 1, pp. 213-24, 1990 (PubMed).