K4023-100
K4023-100? EGF Microplate coated with anti-mouse monoclonal Ab against EGF, 96 wells ? Lyophilized recombinant mouse EGF standard (10 ng/vial) ? Biotinylated anti-mouse EGF antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution? Serum & plasma (heparin, EDTA) ? Cell culture supernatants ? Urine ? Tissue homogenatesEGF (mouse) ELISA Kit: Colorimetric Assay for Quantitative measurement of mouse EGF in serum, plasma, urine, tissue homogenates & cell culture supernatants. Detection Range: 15.6-1000 pg/ml. 100 assays.BioVision’s mouse EGF (Epidermal Growth Factor) ELISA Kit is based on the standard sandwich enzyme-linked immunosorbent assay technology. This assay employs a monoclonal antibody from rat specific for EGF coated on a 96-well plate. Standards (E. Coli, N977-R1029) and test samples are added to the wells and EGF present in a sample is bound to the wells by the immobilized antibody. A biotinylated detection polyclonal antibody from goat specific for EGF is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the mouse EGF captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 15.6 pg/ml – 1000 pg/ml. Sensitivity: < 1 pg/ml.
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K4024-100
K4024-100? EGF Microplate coated with anti-rat monoclonal Ab against EGF, 96 wells ? Lyophilized recombinant rat EGF standard (10 ng/vial) ? Biotinylated anti-rat EGF antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution? Serum & plasma (heparin, EDTA) ? Cell culture supernatants ? Urine ? Tissue homogenatesEGF (rat) ELISA Kit: Colorimetric Assay for Quantitative measurement of rat EGF in serum, plasma, urine, tissue homogenates & cell culture supernatants. Detection Range: 7.8-500 pg/ml. 100 assays.BioVision’s rat EGF (Epidermal Growth Factor) ELISA Kit is based on the standard sandwich enzyme-linked immunosorbent assay technology. This assay employs a monoclonal antibody from mouse specific for EGF coated on a 96-well plate. Standards (E. Coli, N974-R1026) and test samples are added to the wells and EGF present in a sample is bound to the wells by the immobilized antibody. A biotinylated detection polyclonal antibody from goat specific for EGF is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the rat EGF captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 7.8 pg/ml – 500 pg/ml. Sensitivity: < 1 pg/ml.
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K7429-100
K7429-100? Plate coated with mouse MAb to ET-1 ? ET-1 Ab Concentrate ? Antibody Diluent ? Assay Buffer 17 ? Wash Buffer Concentrate ? ET-1 Standard (1000 pg/ml) ? TMB Substrate ? Stop Solution 2 (1 N HCl in H20) ? Plate Sealer Serum, plasma, culture supernatantsEndothelin-1 (ET-1) ELISA Kit: Rapid & convenient colorimetric assay for quantitative measurement of human, mouse, rat, cow, dog, pig and rabbit ET-1. Sensitivity: 0.4 pg/ml (range: 0.78-100 pg/ml). 100 assays. BioVision’s Endothelin-1 (ET-1) ELISA kit is a competitive immunoassay for the quantitative determination of Endothelin-1 in biological fluids. ET-1 has identical amino acid sequence for human, mouse, rat, cow, dog, pig, and rabbit. The basal circulating level of ET-1 is reported to be < 1 to 3pg/mL but is known to be elevated in atrial and pulmonary hypertensions, atherosclerosis, congestive heart failure, cancer and variably related to lung diseases such as COPD and asthma. Samples and standards are added to wells coated with a monoclonal antibody specific for ET-1 and incubated. The plate is washed, leaving only bound ET-1 on the plate. A solution of HRP labeled monoclonal antibody to ET-1 is then added. This binds the ET-1 captured on the plate. The plate is then incubated. The plate is washed to remove excess HRP labeled antibody. TMB Substrate solution is added. The substrate generates a blue color when catalyzed by the HRP. Stop solution is added to stop the substrate reaction. The resulting yellow color is read at 450 nm. The amount of signal is directly proportional to the level of ET-1 in the sample. Sensitivity: 0.4 pg/ml (range: 0.78-100 pg/ml). The intra-Assay reproducibility is CV<10% & inter-Assay is CV<12%. Cross Reactivity: ET-1: 100%, ET-2: 21%, ET-3: 3.6%, human Big ET-1: <0.1%, rat Big ET-1: <0.1%, human Big ET-2: <0.1%, human Big ET-3 amide: <0.1%.
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K3829-100
K3829-100? 96 wells coated with anti-human Estradiol antibody, 1 Microplate with 2 adhesive strips ? Human Estradiol standard (72 pmol/L) ? HRP-conjugate reagent ? Standard Diluent ? Sample diluent ? Chromogen Solution A ? Chromogen Solution B ? Stop Solution ? Wash Solution (30x stock) ? Serum & plasma (EDTA/Citrate), urine ? Cell culture medium, tissue homogenates and cell lysates Estradiol E2 (human) ELISA Kit: Colorimetric Assay for Quantitative measurement of human Estradiol (E2 or 17β-estradiol) in serum, plasma, urine, cell culture media and cell/tissue lysates. Detection Range:2 – 50 pmol/L. 100 assays. Estradiol (E2 or 17β-estradiol) is the predominant female reproductive hormone secreted by the ovaries. Smaller amounts of estradiol are also produced by the adrenal cortex, and by the testes in men. BioVision’s human Estradiol E2 ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. Human Estradiol E2 antibody is coated on a 96-well plate. Standards and test samples are added to the wells and Estradiol E2 present in a sample is bound by the immobilized antibody. An HRP-conjugate reagent is added subsequently. After washing away the unbound antibody/HRP conjugates, HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the human Estradiol E2 captured onto the plate. This ELISA kit shows no species cross-reactivity. Detection Range: 2 – 50 pmol/L.
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K3830-100
K3830-100? 96 wells coated with anti-mouse Estradiol antibody, 1 Microplate with 2 adhesive strips ? Mouse Estradiol standard (72 ng/L) ? HRP-conjugate reagent ? Standard Diluent ? Sample diluent ? Chromogen Solution A ? Chromogen Solution B ? Stop Solution ? Wash Solution (30x stock) ? Serum & plasma (EDTA/Citrate), urine ? Cell culture medium, tissue homogenates and cell lysates Estradiol E2 (mouse) ELISA Kit: Colorimetric Assay for Quantitative measurement of mouse Estradiol (E2 or 17β-estradiol) in serum, plasma, urine, cell culture media and cell/tissue lysates. Detection Range:2 – 50 ng/L. 100 assays. Estradiol (E2 or 17β-estradiol) is the predominant female reproductive hormone secreted by the ovaries. Smaller amounts of estradiol are also produced by the adrenal cortex and by the testes. BioVision’s mouse Estradiol E2 ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. Mouse Estradiol E2 antibody is coated on a 96-well plate. Standards and test samples are added to the wells and Estradiol E2 present in a sample is bound by the immobilized antibody. An HRP-conjugate reagent is added subsequently. After washing away the unbound antibody/HRP conjugates, HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the mouse Estradiol E2 captured onto the plate. This ELISA kit shows no species cross-reactivity. Detection Range: 2 – 50 ng/L.
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K3831-100
K3831-100? 96 wells coated with anti-rat Estradiol antibody, 1 Microplate with 2 adhesive strips ? Rat Estradiol standard (72 ng/L) ? HRP-conjugate reagent ? Standard Diluent ? Sample diluent ? Chromogen Solution A ? Chromogen Solution B ? Stop Solution ? Wash Solution (30x stock) ? Serum & plasma (EDTA/Citrate), urine ? Cell culture medium, tissue homogenates and cell lysates Estradiol E2 (rat) ELISA Kit: Colorimetric Assay for Quantitative measurement of rat Estradiol (E2 or 17β-estradiol) in serum, plasma, urine, cell culture media and cell/tissue lysates. Detection Range:2 – 50 ng/L. 100 assays. Estradiol (E2 or 17β-estradiol) is the predominant female reproductive hormone secreted by the ovaries. Smaller amounts of estradiol are also produced by the adrenal cortex and by the testes. BioVision’s rat Estradiol E2 ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. Rat Estradiol E2 antibody is coated on a 96-well plate. Standards and test samples are added to the wells and Estradiol E2 present in a sample is bound by the immobilized antibody. An HRP-conjugate reagent is added subsequently. After washing away the unbound antibody/HRP conjugates, HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the rat Estradiol E2 captured onto the plate. This ELISA kit shows no species cross-reactivity. Detection Range: 2 – 50 ng/L.
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K4765-100
K4765-100? Fas Ligand Microplate (Item A) coated with anti-human Fas Ligand, 96 wells ? Wash Buffer Concentrate (20x) (Item B) ? Standards (Item C) (recombinant human Fas Ligand) ? Assay Diluent A (Item D) for Standard/Sample (serum/plasma) diluent (0.09% sodium azide as preservative) ? Assay Diluent B (Item E) for Standard/Sample (cell culture medium/urine) diluent. (5x concentrated) ? Detection Antibody Fas Ligand (Item F), biotinylated anti-human Fas Ligand (each vial enough for half plate) ? HRP-Streptavidin Concentrate (Item G), 200x concentrated ? TMB One-Step Substrate Reagent (Item H) 3,3’,5,5’-tetramethylbenzidine (TMB) in buffer solution ? Stop Solution (Item I), 0.2 M sulfuric acid ? Serum & plasma ? Cell culture supernatants ? UrineHuman Fas Ligand (FasL) ELISA Kit: Colorimetric Assay for Quantitative Determination of human FasL in Serum, Plasma, Urine & Cell culture supernatants. Detection Range: 2 pg/ml - 1000 pg/ml. 100 assays. BioVision’s Human Fas Ligand ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of human Fas Ligand. This assay employs an antibody specific for human Fas Ligand coated on a 96-well plate. Standards and samples are pipetted into the wells and Fas Ligand present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-human Fas Ligand antibody is added. After washing away unbound biotinylated antibody, HRP-conjugated streptavidin is pipetted to the wells. The wells are again washed, a TMB substrate solution is added to the wells and color develops in proportion to the amount of Fas Ligand bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm. This ELISA kit shows no cross-reactivity with the following cytokines tested: human Angiogenin, BDNF,BLC, ENA-78, FGF-4, IL-1α, IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-11, IL-12 p70, IL-12 p40, IL-13, IL-15, IL-309, IP-10, G-CSF, GM-CSF, IFN-γ, Leptin (OB), MCP-1, MCP-2, MCP-3, MDC, MIP-1α, MIP-1β, MIP-1δ, PARC, PDGF, RANTES, SCF, TARC, TGF-β, TIMP-1, TIMP-2, TNF-α, TNF-β, TPO, VEGF. The minimum detectable dose of Fas Ligand is typically less than 2 pg/ml. Detection Range: 2 pg/ml - 1000 pg/ml. The intra-Assay reproducibility is CV<10% & inter-Assay is CV<12%.
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K3331-100
K3331-100? FasL Microplate coated with anti-mouse Ab against FasL, 96 wells ? Lyophilized recombinant mouse FasL standard (10 ng/vial) ? Biotinylated anti-mouse FasL antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution? Serum & plasma ? Cell culture supernatantsFas Ligand (mouse) ELISA Kit: Colorimetric Assay for Quantitative measurement of mouse FasL in serum, plasma & cell culture supernatants. Detection Range: 15.6-1000 pg/ml. 100 assays.BioVision’s mouse FasL (Fas Ligand, CD95L) ELISA Kit is based on the standard sandwich enzyme-linked immunosorbent assay technology. This assay employs a monoclonal antibody form rat specific for FasL coated on a 96-well plate. Standards (NSO, P132-L279) and test samples are added to the wells and FasL present in a sample is bound to the wells by the immobilized antibody. A biotinylated detection polyclonal antibody from goat specific for FasL is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, Avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the mouse Fas L captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 15.6 pg/ml – 1000 pg/ml. Sensitivity: < 10 pg/ml.
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K3330-100
K3330-100? FasL Microplate coated with anti-rat Ab against FasL, 96 wells ? Lyophilized recombinant rat FasL standard (10 ng/vial) ? Biotinylated anti-rat FasL antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution? Serum & plasma ? Cell culture supernatantsFas Ligand (rat) ELISA Kit: Colorimetric Assay for Quantitative measurement of rat FasL in serum, plasma & cell culture supernatants. Detection Range: 31.2-2000 pg/ml. 100 assays.BioVision’s rat FasL ELISA Kit is based on the standard sandwich enzyme-linked immunosorbent assay technology. This assay employs a monoclonal antibody form mouse specific for FasL coated on a 96-well plate. Standards (NSO, Q127-L278) and test samples are added to the wells and FasL present in a sample is bound to the wells by the immobilized antibody. A biotinylated detection polyclonal antibody from goat specific for FasL is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, Avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the rat FasL captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 31.2 pg/ml – 2000 pg/ml. Sensitivity: < 10 pg/ml.
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K7420-100
K7420-100? Microplate coated with Ferritin MAb, 96 wells ? Ferritin Standard: (0.5 ml) (ready to use) ? Incubation Buffer (ready to use) ? Enzyme Conjugate (ready to use) ? Wash Concentrate (20X) ? TMB Substrate (ready to use) ? Stop Solution (ready to use) Serum or plasma Ferritin (human) ELISA Kit: Rapid & convenient colorimetric assay for quantitative measurement of human Ferritin in serum or plasma. 100 assays. Human Ferritin has a molecular weight of approximately 450,000 Daltons, and consists of a protein shell around an iron core; each molecule of Ferritin may contain as many as 4,000 iron atoms. Under normal conditions, this may represent 25% of the total iron found in the body. In addition, Ferrritin can be found in several isomers. High concentrations of Ferritin are found in the cytoplasm of the reticuloendothelial system, the liver, spleen and bone marrow. Methods previously used to measure iron in such tissues are invasive, cause patient trauma and lack adequate sensitivity. The measurement of Ferritin in serum is useful in determining changes in body iron storage, and is non-invasive with relatively little patient discomfort. Serum Ferritin levels can be measured routinely and are particularly useful in the early detection of iron- deficiency anemia in apparently healthy people. Serum Ferritin measurements are also clinically significant in the monitoring of the iron status of pregnant women, blood donors, and renal dialysis patients. High Ferritin levels may indicate iron overload without apparent liver damage, as may be noted in the early stages of idiopathic hemochromatosis. Ferritin levels in serum have also been used to evaluate clinical conditions not related to iron storage, including inflammation, chronic liver disease, and malignancy. BioVision’s Ferritin kit is a solid phase direct sandwich ELISA Kit. The standards, samples, and controls are added to the wells coated with monoclonal antibody to Ferritin. Ferritin in the sample, standards & controls binds to anti-Ferritin Mab on the well and the anti-Ferritin HRP then binds to Ferritin. Unbound Protein and HRP conjugate is washed off by wash buffer. Upon the addition of the substrate, the intensity of color is proportional to the concentration of Ferritin in the samples. A standard curve is prepared relating color intensity to the concentration of the Ferritin.
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K3631-100
K3631-100? 96 wells coated with anti-human polyclonal Fibronectin antibody, 1 Microplate ? Lyophilized native human Fibronectin standard (10 ng/vial) ? Biotinylated anti- human Fibronectin antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution ? Serum & plasma (heparin, EDTA, Citrate) ? Cell culture supernatants Fibronectin (human) ELISA Kit: Colorimetric Assay for Quantitative measurement of human Fibronectin in serum, plasma & cell culture supernatants.Sensitivity: < 10 pg/ml. 100 assays. Fibronectin is a 430 KDa dimeric glycoprotein that exists in 2 forms - cellular and plasma fibronectin. BioVision’s human Fibronectin ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. A rabbit polyclonal antibody specific for human Fibronectin is coated on a 96-well plate. Standards and test samples are added to the wells and Fibronectin present in a sample is bound by the immobilized antibody. A biotinylated polyclonal antibody from goat specific for Fibronectin is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the human Fibronectin captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 156 pg/ml – 10,000 pg/ml. Sensitivity: < 10 pg/ml.
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K3632-100
K3632-100? 96 wells coated with anti-mouse monoclonal Fibronectin antibody, 1 Microplate ? Lyophilized native mouse Fibronectin standard (10 ng/vial) ? Biotinylated anti-mouse Fibronectin antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution ? Serum & plasma (heparin, EDTA, Citrate) ? Cell culture supernatants Fibronectin (mouse) ELISA Kit: Colorimetric Assay for Quantitative measurement of mouse Fibronectin in serum, plasma & cell culture supernatants. Sensitivity: < 15 pg/ml. 100 assays. Fibronectin is a 430 KDa dimeric glycoprotein that exists in 2 forms - cellular and plasma fibronectin. BioVision’s mouse Fibronectin ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. A rat monoclonal antibody specific for mouse Fibronectin is coated on a 96-well plate. Standards and test samples are added to the wells and Fibronectin present in a sample is bound by the immobilized antibody. A biotinylated polyclonal antibody from goat specific for Fibronectin is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the mouse Fibronectin captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 156 pg/ml – 10,000 pg/ml. Sensitivity: < 15 pg/ml.
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K3633-100
K3633-100? 96 wells coated with anti-rat monoclonal Fibronectin antibody, 1 Microplate ? Lyophilized native rat Fibronectin standard (10 ng/vial) ? Biotinylated anti-rat Fibronectin antibody ? Avidin-Biotin-Peroxidase Complex (ABC) ? Sample diluent buffer ? Antibody diluent buffer ? ABC diluent buffer ? TMB color developing agent (Colorless) ? TMB stop solution ? Serum & plasma (heparin, EDTA) ? Cell culture supernatants Fibronectin (rat) ELISA Kit: Colorimetric Assay for Quantitative measurement of rat Fibronectin in serum, plasma & cell culture supernatants.Sensitivity: < 15 pg/ml. 100 assays. Fibronectin is a 430 KDa dimeric glycoprotein that exists in 2 forms - cellular and plasma fibronectin. BioVision’s rat Fibronectin ELISA Kit is based on the standard principle of a sandwich enzyme-linked immunosorbent assay. A mouse monoclonal antibody specific for rat Fibronectin is coated on a 96-well plate. Standards and test samples are added to the wells and Fibronectin present in a sample is bound by the immobilized antibody. A biotinylated polyclonal antibody from goat specific for Fibronectin is added subsequently. After washing away the unbound biotinylated antibody with PBS or TBS buffer, avidin-Biotin-Peroxidase Complex is added to the wells. The wells are again washed with PBS or TBS buffer to remove the unbound conjugates. HRP substrate TMB is used to visualize the HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue product that changes into yellow after adding acidic stop solution. The density of yellow color is proportional to the rat Fibronectin captured onto the plate. This ELISA kit shows no cross-reactivity with other relevant proteins. Detection Range: 156 pg/ml – 10,000 pg/ml. Sensitivity: < 15 pg/ml.
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3939-200
Beta3-AR Antibody Host:Rabbit Antibody Type:Polyclonal Species Reactivity:Rat Application:Western blot Western blot analysis (1-4 μg/ml). However, the optimal conditions should be determined individually. Rat kidney tissue lysate can be used as a positive control.
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3940-200
AdipoR1 Antibody Host:Rabbit Antibody Type:Polyclonal Species Reactivity:Mouse Application:Western blot Western blot analysis (1-4 μg/ml). However, the optimal conditions should be determined individually. 3T3 cell lysate can be used as a positive control.
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