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Fibronectin 1 Kit ELISA

Ce kit ELISA Colorimetric est destiné à la mesure quantitative de Souris Fibronectin 1. Il a été cité dans 11 publications.
N° du produit ABIN921056
664,40 €
Plus frais de livraison 40,00 € et TVA
96 tests
Destination: France
Envoi sous 8 à 12 jours ouvrables

Aperçu rapide pour Fibronectin 1 Kit ELISA (ABIN921056)

Antigène

Voir toutes Fibronectin 1 (FN1) Kits ELISA
Fibronectin 1 (FN1)

Reactivité

  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Souris

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

156 pg/mL - 10000 pg/mL

Application

ELISA

Type d'échantillon

Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA), Plasma (citrate)
  • Seuil minimal de détection

    156 pg/mL

    Fonction

    Sandwich Mouse Fibronectin ELISA Kit to quantitate Mouse Fn1 in cell culture supernatants, serum and plasma (heparin, EDTA, citrate).

    Analytical Method

    Quantitative

    Specificité

    Target protein isolated from mouse plasma

    Capture antibody and Detection antibody: polyclonal antibody from rabbit, polyclonal antibody from rabbit

    Réactivité croisée (Details)

    There is no detectable cross-reactivity with other relevant proteins.

    Sensibilité

    < 15 pg/mL

    Ingrédients

    1. Pre-coated 96-well strip microplate
    2. Standard
    3. Biotinylated antibody (100x)
    4. Avidin-Biotin-Peroxidase Complex (100x)
    5. Sample Diluent
    6. Antibody Diluent
    7. Avidin-Biotin-Peroxidase Diluent
    8. Color Developing Reagent (TMB)
    9. Stop Solution
    10. Wash Buffer (25x)
    11. Adhesive plate sealers

    Matériel non inclus

    Microplate Reader capable of reading absorbance at 450nm. Incubator. Automated plate washer (optional). Pipettes and pipette tips capable of precisely dispensing 0.5 μL through 1 mL volumes of aqueous solutions. Multichannel pipettes are recommended for large amount of samples. Deionized or distilled water. 500 mL graduated cylinders. Test tubes for dilution.
  • Indications d'application

    Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.

    Volume d'échantillon

    100 μL

    Plaque

    Pre-coated

    Protocole

    ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. An antibody has been precoated onto 96-well plates. Standards and test samples are added to the wells, a biotinylated detection antibody specific for target is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount in sample captured in plate.

    Précision du teste

    Intra-Assay Precision (CV%): 6.5%, 7.5%, 6.8%
    Inter-Assay Precision (CV%): 7.1%, 8.7%, 8.5%

    Restrictions

    For Research Use only
  • Conseil sur la manipulation

    Avoid multiple freeze-thaw cycles.

    Stock

    -20 °C,4 °C

    Stockage commentaire

    Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)

    Date de péremption

    12 months
  • Zhao, Xu, Sun, Ma, Wu, Xu, Kuang: "Tuning the interactions between chiral plasmonic films and living cells." dans: Nature communications, Vol. 8, Issue 1, pp. 2007, (2018) (PubMed).

    Bai, Li, Zhao, Li, Li, Feng, Qin, Tian, Zhou: "A Chinese Herbal Formula Ameliorates Pulmonary Fibrosis by Inhibiting Oxidative Stress via Upregulating Nrf2." dans: Frontiers in pharmacology, Vol. 9, pp. 628, (2018) (PubMed).

    Rani, Nicholson, Zhang, Schwacha: "Damage-associated molecular patterns (DAMPs) released after burn are associated with inflammation and monocyte activation." dans: Burns : journal of the International Society for Burn Injuries, Vol. 43, Issue 2, pp. 297-303, (2017) (PubMed).

    Lv, Wu, Zhou, Shao, Wang, Wang: "Alpha Lipoic Acid Modulated High Glucose-Induced Rat Mesangial Cell Dysfunction via mTOR/p70S6K/4E-BP1 Pathway." dans: International journal of endocrinology, Vol. 2014, pp. 658589, (2014) (PubMed).

    Xu, Guan, Zheng, Gao, Zeng, Qin, Xue: "Exendin-4 alleviates high glucose-induced rat mesangial cell dysfunction through the AMPK pathway." dans: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 33, Issue 2, pp. 423-32, (2014) (PubMed).

    Gao, Huang, Li: "NOX1 abet mesangial fibrogenesis via iNOS induction in diabetes." dans: Molecular and cellular biochemistry, Vol. 382, Issue 1-2, pp. 185-91, (2013) (PubMed).

    Bai, Zeng, Zhou, Liao, Zhang, Xu, Han, Pei, Liu, Liu, Yao, Xu: "Cdc42-interacting protein-4 promotes TGF-?1-induced epithelial-mesenchymal transition and extracellular matrix deposition in renal proximal tubular epithelial cells." dans: International journal of biological sciences, Vol. 8, Issue 6, pp. 859-69, (2012) (PubMed).

    Yang, Cheng, Liu, Lu, Song, Jiang, Wu, Guo: "Comparison of mesenchymal stem cells released from poly(N-isopropylacrylamide) copolymer film and by trypsinization." dans: Biomedical materials (Bristol, England), Vol. 7, Issue 3, pp. 35003, (2012) (PubMed).

    Mao, Gao, Li, Li: "Pigment epithelium-derived factor inhibits high glucose induced oxidative stress and fibrosis of cultured human glomerular mesangial cells." dans: Saudi medical journal, Vol. 32, Issue 8, pp. 769-77, (2011) (PubMed).

    Zeng, Han, Luo, Li, Pei, Liao, Bai, Ge, Liu, Xu: "Role of Sema4C in TGF-?1-induced mitogen-activated protein kinase activation and epithelial-mesenchymal transition in renal tubular epithelial cells." dans: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, Vol. 26, Issue 4, pp. 1149-56, (2011) (PubMed).

    Tang, Song, Shi, Yuan, Li: "Dicer knockdown induces fibronectin-1 expression in HEK293T cells via induction of Egr1." dans: Biochimica et biophysica acta, Vol. 1800, Issue 3, pp. 380-4, (2010) (PubMed).

  • Antigène Voir toutes Fibronectin 1 (FN1) Kits ELISA

    Fibronectin 1 (FN1)

    Autre désignation

    FN1

    Sujet

    Background: Fibronectin (FN) also known as LETS, is identified on the surfFN of fibroblasts by labeling with radioactive compounds or specific antibodies. Fibronectin is a 430,000-dalton dimeric glycoprotein that exists in 2 forms, termed cellular and plasma fibronectin. Cellular and plasma fibronectins are heterodimers consisting of similar but not identical polypeptides. These two forms of FN differ in biologic activity. Fibronectins bind cell surfFNs and various compounds including collagen, fibrin, heparin, DNA, and actin. Because fibronectin stimulates endocytosis in several systems and promotes the clearance of particulate material from the circulation, it could function in the clearance of C1q-coated material such as immune complexes or cellular debris. Fibronectins are involved in cell adhesion, cell motility, opsonization, would healing, and maintenance of cell shape. LETS, encoded on chromosome 8, is responsible for the LETS protein expression in humans. Because LETS has been implicated in tumorigenicity and cellular transformation, it is of interest that rearrangement or modifications in the number of chromosome 8 have been associated with certain forms of cancer.

    Gene Full Name: fibronectin 1

    ID gène

    14268

    UniProt

    P11276

    Pathways

    Cellular Response to Molecule of Bacterial Origin, Carbohydrate Homeostasis, Autophagy
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