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Fibronectin 1 ELISA 试剂盒

人 Fibronectin 1 ELISA Kit, Colorimetric is an assay for quantification of 人 Fibronectin 1, that has been mentioned in 13+ publications.
产品编号 ABIN411271
发货至: 中国
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Quick Overview for Fibronectin 1 ELISA 试剂盒 (ABIN411271)

抗原

See all Fibronectin 1 (FN1) ELISA试剂盒
Fibronectin 1 (FN1)

适用

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检测方法

Colorimetric

实验类型

Sandwich ELISA

检测范围

156 pg/mL - 10000 pg/mL

应用范围

ELISA

样品类型

Cell Culture Supernatant, Serum, Plasma (heparin), Plasma (EDTA), Plasma (citrate)
  • 最低检测浓度

    156 pg/mL

    原理

    Sandwich Human Fibronectin ELISA Kit to quantitate Human FN1 in cell culture supernatants, serum and plasma (heparin, EDTA, citrate).

    Analytical Method

    Quantitative

    特异性

    Target protein isolated from human plasma

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

    交叉反应 (详细)

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

    灵敏度

    < 10 pg/mL

    组件

    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

    试剂未包括

    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.
  • 应用备注

    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.

    样本量

    100 μL

    板类型

    Pre-coated

    实验流程

    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.

    实验精密度

    Intra-Assay Precision (CV%): 4.6%, 5.7%, 5.7%
    Inter-Assay Precision (CV%): 5.7%, 6.9%, 7%

    限制

    仅限研究用
  • 注意事项

    Avoid multiple freeze-thaw cycles.

    储存条件

    -20 °C,4 °C

    储存方法

    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.)

    有效期

    12 months
  • Stevens, Scull, Ramanan, Fortin, Chaturvedi, Knouse, Xiao, Fung, Mirabella, Chen, McCue, Yang, Fleming, Chung, de Jong, Chen, Rice, Bhatia: "In situ expansion of engineered human liver tissue in a mouse model of chronic liver disease." in: Science translational medicine, Vol. 9, Issue 399, (2018) (PubMed).

    Banville, Burgess, Jaffar, Tjin, Richeldi, Cerri, Persiani, Black, Oliver: "A quantitative proteomic approach to identify significantly altered protein networks in the serum of patients with lymphangioleiomyomatosis (LAM)." in: PLoS ONE, Vol. 9, Issue 8, pp. e105365, (2014) (PubMed).

    Lv, Wu, Zhou, Shao, Wang, Wang: "Alpha Lipoic Acid Modulated High Glucose-Induced Rat Mesangial Cell Dysfunction via mTOR/p70S6K/4E-BP1 Pathway." in: 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." in: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology, Vol. 33, Issue 2, pp. 423-32, (2014) (PubMed).

    Inoue, Sasaki, Katada, Taguchi: "Quantitative biocompatibility evaluation of nickel-free high-nitrogen stainless steel in vitro/in vivo." in: Journal of biomedical materials research. Part B, Applied biomaterials, Vol. 102, Issue 1, pp. 68-72, (2014) (PubMed).

    Zirkel, Lederer, Stöhr, Pazaitis, Hüttelmaier: "IGF2BP1 promotes mesenchymal cell properties and migration of tumor-derived cells by enhancing the expression of LEF1 and SNAI2 (SLUG)." in: Nucleic acids research, Vol. 41, Issue 13, pp. 6618-36, (2013) (PubMed).

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

    Sasaki, Inoue, Katada, Taguchi: "Promotion of initial cell adhesion on trisuccinimidyl citrate-modified nickel-free high-nitrogen stainless steel." in: Journal of materials science. Materials in medicine, Vol. 24, Issue 4, pp. 951-8, (2013) (PubMed).

    Yang, Cheng, Liu, Lu, Song, Jiang, Wu, Guo: "Comparison of mesenchymal stem cells released from poly(N-isopropylacrylamide) copolymer film and by trypsinization." in: Biomedical materials (Bristol, England), Vol. 7, Issue 3, pp. 35003, (2012) (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." in: International journal of biological sciences, Vol. 8, Issue 6, pp. 859-69, (2012) (PubMed).

    Mao, Gao, Li, Li: "Pigment epithelium-derived factor inhibits high glucose induced oxidative stress and fibrosis of cultured human glomerular mesangial cells." in: 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." in: 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." in: Biochimica et biophysica acta, Vol. 1800, Issue 3, pp. 380-4, (2010) (PubMed).

  • 抗原 See all Fibronectin 1 (FN1) ELISA试剂盒

    Fibronectin 1 (FN1)

    别名

    FN1

    背景

    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. The standard used in this kit is isolated from human plasma with the molecular mass of 200-250KDa.

    Gene Full Name: fibronectin 1

    基因ID

    2335

    UniProt

    P02751

    途径

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