Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

FGF2 Kit ELISA

FGF2 Reactivité: Souris Colorimetric Sandwich ELISA 8-600 pg/mL Cell Culture Supernatant, Plasma, Serum
N° du produit ABIN625113
  • Antigène Voir toutes FGF2 Kits ELISA
    FGF2 (Fibroblast Growth Factor 2 (Basic) (FGF2))
    Reactivité
    • 10
    • 5
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Souris
    Méthode de détection
    Colorimetric
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    8-600 pg/mL
    Seuil minimal de détection
    8 pg/mL
    Application
    ELISA
    Fonction
    Mouse bFGF ELISA Kit for cell culture supernatants, plasma, and serum samples.
    Type d'échantillon
    Serum, Plasma, Cell Culture Supernatant
    Analytical Method
    Quantitative
    Specificité
    This ELISA kit shows no cross-reactivity with following cytokines tested: Mouse CD30, L CD30, T CD40, CRG-2, CTACK, CXCL16, Eotaxin , Eotaxin-2, Fas Ligand, Fractalkine, GCSF, GM-CFS, IFN- gamma, IGFBP-3, IGFBP-5, IGFBP-6, IL-1 alpha, IL-1 beta, IL-2, IL-3, IL-3 Rb, IL-4, IL-5, IL-9, IL-10, IL-12 p40/p70, IL-12 p70, IL-13, IL-17, KC, Leptin R, LEPTIN(OB), LIX, L-Selectin, Lymphotactin, MCP-1, MCP-5, M-CSF, MIG, MIP-1 alpha, MIP-1 gamma, MIP-2, MIP-3 beta, MIP-3 alpha, PF-4, P-Selectin, RANTES, SCF, SDF-1 alpha, TARC, TCA-3, TECK, TIMP-1, TNF-alpha, TNF RI, TNF RII, TPO, VCAM-1, VEGF.
    Sensibilité
    < 8 pg/mL
    Attributs du produit
    • Strip plates and additional reagents allow for use in multiple experiments
    • Quantitative protein detection
    • Establishes normal range
    • The best products for confirmation of antibody array data
    Ingrédients
    • Pre-Coated 96-well Strip Microplate
    • Wash Buffer
    • Stop Solution
    • Assay Diluent(s)
    • Lyophilized Standard
    • Biotinylated Detection Antibody
    • Streptavidin-Conjugated HRP
    • TMB One-Step Substrate
    Matériel non inclus
    • Distilled or deionized water
    • Precision pipettes to deliver 2 μL to 1 μL volumes
    • Adjustable 1-25 μL pipettes for reagent preparation
    • 100 μL and 1 liter graduated cylinders
    • Tubes to prepare standard and sample dilutions
    • Absorbent paper
    • Microplate reader capable of measuring absorbance at 450nm
    • Log-log graph paper or computer and software for ELISA data analysis
    Featured
    Discover our best selling FGF2 Kit ELISA
    Top Product
    Discover our top product FGF2 Kit ELISA
  • Indications d'application
    Recommended Dilution for serum and plasma samples2 - 10 fold
    Volume d'échantillon
    100 μL
    Plaque
    Pre-coated
    Protocole
    1. Prepare all reagents, samples and standards as instructed in the manual.
    2. Add 100 μL of standard or sample to each well.
    3. Incubate 2.5 h at RT or O/N at 4 °C.
    4. Add 100 μL of prepared biotin antibody to each well.
    5. Incubate 1 h at RT.
    6. Add 100 μL of prepared Streptavidin solution to each well.
    7. Incubate 45 min at RT.
    8. Add 100 μL of TMB One-Step Substrate Reagent to each well.
    9. Incubate 30 min at RT.
    10. Add 50 μL of Stop Solution to each well.
    11. Read at 450 nm immediately.
    Préparation des réactifs
    1. Bring all reagents and samples to room temperature (18 - 25 °C) before use.
      2. Sample dilution: Assay Diluent A (Item D) should be used for dilution of serum/plasma samples. 1x Assay Diluent B should be used for dilution of cell culture supernates. Suggested dilution for normal serum/plasma: 2-10 fold. Please note that levels of the target protein may vary between different specimens. Optimal dilution factors for each sample must be determined by the investigator.
      3. Assay Diluent B should be diluted 5-fold with deionized or distilled water before use.
      4. reparation of standard: Briefly spin the vial of Item C and then add 400 µL Assay Diluent A (for serum/plasma samples) or 1x Assay Diluent B (for cell culture supernates) into Item C vial to prepare a 50 ng/mL standard. Dissolve the powder thoroughly by a gentle mix. Add 12 µL bFGF standard (50 ng/mL) from the vial of Item C, into a tube with 988 µL Assay Diluent A or 1x Assay Diluent B to prepare a 600 pg/mL stock standard solution. Pipette 300 µL Assay Diluent A or 1x Assay Diluent B into each tube. Use the stock standard solution to produce a dilution series . Mix each tube thoroughly before the next transfer. Assay Diluent A or 1x Assay Diluent B serves as the zero standard (0 pg/mL). 300 µL 300 µL 300 µL 300myl 12 µL standard + 988 µL 300 µL 600 300 150 75 37.5 18.8 0 pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL
      5. If the Wash Concentrate (20x) (Item B) contains visible crystals, warm to room temperature and mix gently until dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to yield 400 ml of 1x Wash Buffer.
      6. Briefly spin the Detection Antibody vial (Item F) before use. Add 100 µL of 1x Assay Diluent B into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently (the concentrate can be stored at 4 °C for 5 days). The detection antibody concentrate should be diluted 80-fold with 1x Assay Diluent B and used in step 4 of Part VI Assay Procedure.
      7. Briefly spin the HRP-Streptavidin concentrate vial (Item G) and pipette up and down to mix gently before use. HRP-Streptavidin concentrate should be diluted 300-fold with 1x Assay Diluent B. For example: Briefly spin the vial (Item G) and pipette up and down to mix gently . Add 40 µL of HRP-Streptavidin concentrate into a tube with 12 ml 1x Assay Diluent B to prepare a final 300 fold diluted HRP- Streptavidin solution (don't store the diluted solution for next day use). Mix well.
    Procédure de l'essai
    1. Bring all reagents and samples to room temperature (18 - 25 °C) before use. It is recommended that all standards and samples be run at least in duplicate.
      2. Add 100 µL of each standard (see Reagent Preparation step 2) and sample into appropriate wells. Cover well and incubate for 2.5 hours at room temperature or over night at 4 °C with gentle shaking.
      3. Discard the solution and wash 4 times with 1x Wash Solution. Wash by filling each well with Wash Buffer (300 myl) using a multi-channel Pipette or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.
      4. Add 100 µL of 1x prepared biotinylated antibody (Reagent Preparation step 6) to each well. Incubate for 1 hour at room temperature with gentle shaking.
      5. Discard the solution. Repeat the wash as in step
      6. Add 100 µL of prepared Streptavidin solution (see Reagent Preparation step 7) to each well. Incubate for 45 minutes at room temperature with gentle shaking.
      7. Discard the solution. Repeat the wash as in step
      8. Add 100 µL of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with gentle shaking.
      9. Add 50 µL of Stop Solution (Item I) to each well. Read at 450 nm immediately.
    Calcul des résultats

    Calculate the mean absorbance for each set of duplicate standards, controls and samples, and subtract the average zero standard optical density. Plot the standard curve on log-log graph paper or using Sigma plot software, with standard concentration on the x-axis and absorbance on the y-axis. Draw the best-fit straight line through the standard points.
    Typical Data: These standard curves are for demonstration only. A standard curve must be run with each assay. Mouse bFGF concentration (pg/mL) 10 100 1000 O D =4 50 n m 0.01 0.1 1 10 Assay Diluent A Mouse bFGF concentration (pg/mL) 10 100 1000 O D =4 50 n m 0.01 0.1 1 10 Assay Diluent B
    Sensitivity: The minimum detectable dose of bFGF is typically less than 8 pg/mL.
    Recovery: Recovery was determined by spiking various levels of mouse bFGF into mouse serum, plasma and cell culture media. Mean recoveries are as follows: Sample Type Average % Recovery Range ( %) Serum 84.63 78-100 Plasma 83.26 76-99 Cell culture media 119.7 105-129
    Linearity: Sample Type Serum Plasma Cell Culture Media 1:2 Average % of Expected 99.78 87.8 78.9 Range ( %) 91-112 81-94 71-90 1:4 Average % of Expected 96.54 89.8 85.2 Range ( %) 87-115 79-102 74-98
    Reproducibility: Intra-Assay: CV<10 % Inter-Assay: CV<12 %

    Précision du teste
    Intra-Assay: CV< 10 % Inter-Assay: CV< 12 %
    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    The entire kit may be stored at -20°C for up to 1 year from the date of shipment. Avoid repeated freeze-thaw cycles. The kit may be stored at 4°C for up to 6 months. For extended storage, it is recommended to store at -80°C.
    Date de péremption
    6 months
  • Huey, Smith, Sulaeman, Breen: "Skeletal myofiber VEGF is necessary for myogenic and contractile adaptations to functional overload of the plantaris in adult mice." dans: Journal of applied physiology (Bethesda, Md. : 1985), Vol. 120, Issue 2, pp. 188-95, (2016) (PubMed).

    Li, Wang, Huang, Zhang, Yao, Wang, Lv, An, Corrigan, Huang, Ying: "Distinct sustained structural and functional effects of interleukin-33 and interleukin-25 on the airways in a murine asthma surrogate." dans: Immunology, Vol. 145, Issue 4, pp. 508-18, (2015) (PubMed).

    Okamoto, Honda, Doi, Ishizu, Katagiri, Wada, Tomita, Ohtake, Kaneko, Kobayashi, Nangaku, Tokunaga, Noiri: "Glypican-5 Increases Susceptibility to Nephrotic Damage in Diabetic Kidney." dans: The American journal of pathology, Vol. 185, Issue 7, pp. 1889-98, (2015) (PubMed).

    Ozaki, Somamoto, Kawabata, Tabata: "Effect of an artificial silk elastin-like protein on the migration and collagen production of mouse fibroblasts." dans: Journal of biomaterials science. Polymer edition, Vol. 25, Issue 12, pp. 1266-77, (2014) (PubMed).

    Noda, Takii, Parajuli, Kawanokuchi, Sonobe, Takeuchi, Mizuno, Suzumura: "FGF-2 released from degenerating neurons exerts microglial-induced neuroprotection via FGFR3-ERK signaling pathway." dans: Journal of neuroinflammation, Vol. 11, pp. 76, (2014) (PubMed).

    Akiyama, Hasegawa, Hongu, Frohman, Harada, Sakagami, Kanaho: "Trans-regulation of oligodendrocyte myelination by neurons through small GTPase Arf6-regulated secretion of fibroblast growth factor-2." dans: Nature communications, Vol. 5, pp. 4744, (2014) (PubMed).

    Liu, Matson: "Accurate Measurement of Magnetic Resonance Imaging Gradient Characteristics." dans: Materials, Vol. 7, Issue 1, pp. 1-15, (2014) (PubMed).

    Cao, Li, Wang, Wu, Hu, Zhang, Fang, Zhang, Li, Xiong, Yan, Gao, Liu, Li, Sun, Zeng, Zhu, Gao: "Astrocyte-derived ATP modulates depressive-like behaviors." dans: Nature medicine, Vol. 19, Issue 6, pp. 773-7, (2013) (PubMed).

    Yan, DeMars: "Dietary supplementation with methylseleninic acid, but not selenomethionine, reduces spontaneous metastasis of Lewis lung carcinoma in mice." dans: International journal of cancer. Journal international du cancer, Vol. 131, Issue 6, pp. 1260-6, (2012) (PubMed).

    Laschke, Kleer, Scheuer, Schuler, Garcia, Eglin, Alini, Menger: "Vascularisation of porous scaffolds is improved by incorporation of adipose tissue-derived microvascular fragments." dans: European cells & materials, Vol. 24, pp. 266-77, (2012) (PubMed).

    Yan: "Dietary supplementation with curcumin enhances metastatic growth of Lewis lung carcinoma in mice." dans: International journal of cancer. Journal international du cancer, Vol. 132, Issue 2, pp. 269-75, (2012) (PubMed).

    Talbot, Sparks, Powell, Kahl, Caperna: "Quantitative and semiquantitative immunoassay of growth factors and cytokines in the conditioned medium of STO and CF-1 mouse feeder cells." dans: In vitro cellular & developmental biology. Animal, Vol. 48, Issue 1, pp. 1-11, (2012) (PubMed).

    Tsubaki, Yamazoe, Yanae, Satou, Itoh, Kaneko, Kidera, Moriyama, Nishida: "Blockade of the Ras/MEK/ERK and Ras/PI3K/Akt pathways by statins reduces the expression of bFGF, HGF, and TGF-β as angiogenic factors in mouse osteosarcoma." dans: Cytokine, Vol. 54, Issue 1, pp. 100-7, (2011) (PubMed).

    Arenberg, Shambaugh: "Fistulae with off-center prosthesis. A case report with histologic study." dans: Archives of otolaryngology (Chicago, Ill. : 1960), Vol. 90, Issue 3, pp. 275-82 (PubMed).

  • Antigène Voir toutes FGF2 Kits ELISA
    FGF2 (Fibroblast Growth Factor 2 (Basic) (FGF2))
    Autre désignation
    bFGF (FGF2 Produits)
    Synonymes
    BFGF Kit ELISA, FGF-2 Kit ELISA, FGFB Kit ELISA, HBGF-2 Kit ELISA, Fgf-2 Kit ELISA, Fgfb Kit ELISA, bFGF Kit ELISA, fibroblast growth factor 2 Kit ELISA, fibroblast growth factor 2 (basic) Kit ELISA, FGF2 Kit ELISA, Fgf2 Kit ELISA, fgf2 Kit ELISA
    Sujet
    The Mouse bFGF (Fibroblast Growth Factor basic) ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of mouse bFGF in serum, plasma and cell culture supernatants. This assay employs an antibody specific for mouse bFGF coated on a 96-well plate. Standards and samples are pipetted into the wells and bFGF present in a sample is bound to the wells by the immobilized antibody. The wells are washed and biotinylated anti-mouse bFGF 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 bFGF bound. The Stop Solution changes the color from blue to yellow, and the intensity of the color is measured at 450 nm. Reproducibility: Intra-Assay: CV<10% Inter-Assay: CV<12%.
    ID gène
    14173
    UniProt
    P15655
    Pathways
    Signalisation RTK, Fc-epsilon Receptor Signaling Pathway, EGFR Signaling Pathway, Neurotrophin Signaling Pathway, C21-Steroid Hormone Metabolic Process, Inositol Metabolic Process, Glycosaminoglycan Metabolic Process, Protein targeting to Nucleus, S100 Proteins
Vous êtes ici:
Support technique