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GDNF Kit ELISA

Ce kit ELISA Rat GDNF est un kit ELISA Colorimetric conçu pour quantifier Rat GDNF. Ce Kit ELISA a été cité dans 9+ publications.
N° du produit ABIN411276

Aperçu rapide pour GDNF Kit ELISA (ABIN411276)

Antigène

Voir toutes GDNF Kits ELISA
GDNF (Glial Cell Line Derived Neurotrophic Factor (GDNF))

Épitope

AA 78-211

Reactivité

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Rat

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

31.2-2000 pg/mL

Application

ELISA

Type d'échantillon

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

    31.2 pg/mL

    Fonction

    Sandwich High Sensitivity ELISA kit for Quantitative Detection of Rat GDNF

    Marque

    PicoKine™

    Analytical Method

    Quantitative

    Specificité

    Expression system for standard: sf21
    Immunogen sequence: S78-I211

    Réactivité croisée (Details)

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

    Sensibilité

    <4pg/mL

    Matériel non inclus

    Microplate reader in standard size. Automated plate washer. Adjustable pipettes and pipette tips. Multichannel pipettes are recommended in the condition of large amount of samples in the detection. Clean tubes and Eppendorf tubes. Washing buffer (neutral PBS or TBS). Preparation of 0.01M TBS: Add 1.2g Tris, 8.5g Nacl

    Immunogène

    Expression system for standard: sf21
    Immunogen sequence: S78-I211
  • 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.

    Plaque

    Pre-coated

    Protocole

    rat GDNF ELISA Kit was based on standard sandwich enzyme-linked immune-sorbent assay technology. A monoclonal antibody from mouse specific for GDNF has been precoated onto 96-well plates. Standards(sf21, S78-I211) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for GDNF 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 rat GDNF amount of sample captured in plate.

    Procédure de l'essai

    Aliquot 0.1 mL per well of the 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.2pg/mL rat GDNF standard solutions into the precoated 96-well plate. Add 0.1 mL of the sample diluent buffer into the control well (Zero well). Add 0.1 mL of each properly diluted sample of rat cell culture supernates, serum or plasma(heparin, EDTA) to each empty well. See "Sample Dilution Guideline" above for details. We recommend that each rat GDNF standard solution and each sample is measured in duplicate.

    Précision du teste

    • Sample 1: n=16, Mean(pg/ml): 155, Standard deviation: 6.98, CV(%): 4.5
    • Sample 2: n=16, Mean(pg/ml): 624, Standard deviation: 26.21, CV(%): 4.2
    • Sample 3: n=16, Mean(pg/ml): 1316, Standard deviation: 72.38, CV(%): 5.5,
    • Sample 1: n=24, Mean(pg/ml): 148, Standard deviation: 10.06, CV(%): 6.8
    • Sample 2: n=24, Mean(pg/ml): 747, Standard deviation: 59.01, CV(%): 7.9
    • Sample 3: n=24, Mean(pg/ml): 1324, Standard deviation: 102, CV(%): 7.7

    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

    Date de péremption

    12 months
  • Duan, Lu, Wang, Zhang, Mao, Cao, Lin, Zhang, Shuai, Shen: "The long-term fate of mesenchymal stem cells labeled with magnetic resonance imaging-visible polymersomes in cerebral ischemia." dans: International journal of nanomedicine, Vol. 12, pp. 6705-6719, (2018) (PubMed).

    Sun, Zhu, Yin, Guo, Xu, Xiao, Jiang, Guo, Meng, Lu, Wang, Peng: "Differentiation of adipose-derived stem cells into Schwann cell-like cells through intermittent induction: potential advantage of cellular transient memory function." dans: Stem cell research & therapy, Vol. 9, Issue 1, pp. 133, (2018) (PubMed).

    Zhuang, Bu, Hua, Darabi, Cao, Xing: "Gelatin-methacrylamide gel loaded with microspheres to deliver GDNF in bilayer collagen conduit promoting sciatic nerve growth." dans: International journal of nanomedicine, Vol. 11, pp. 1383-94, (2016) (PubMed).

    Ziv-Polat, Shahar, Levy, Skaat, Neuman, Fregnan, Geuna, Grothe, Haastert-Talini, Margel: "The role of neurotrophic factors conjugated to iron oxide nanoparticles in peripheral nerve regeneration: in vitro studies." dans: BioMed research international, Vol. 2014, pp. 267808, (2015) (PubMed).

    Morano, Wrobel, Fregnan, Ziv-Polat, Shahar, Ratzka, Grothe, Geuna, Haastert-Talini: "Nanotechnology versus stem cell engineering: in vitro comparison of neurite inductive potentials." dans: International journal of nanomedicine, Vol. 9, pp. 5289-306, (2015) (PubMed).

    Liu, Wang, Shao, Liu: "Genetically modified Schwann cells producing glial cell line-derived neurotrophic factor inhibit neuronal apoptosis in rat spinal cord injury." dans: Molecular medicine reports, Vol. 9, Issue 4, pp. 1305-12, (2014) (PubMed).

    Banerjee, Nürnberger, Hennerbichler, Riedl, Schuh, Hacobian, Teuschl, Eibl, Redl, Wolbank: "In toto differentiation of human amniotic membrane towards the Schwann cell lineage." dans: Cell and tissue banking, Vol. 15, Issue 2, pp. 227-39, (2014) (PubMed).

    Chai, Guo, Li, Wang, Wang, Shi, Hu, Liu, Adah: "Scutellarin and caffeic acid ester fraction, active components of Dengzhanxixin injection, upregulate neurotrophins synthesis and release in hypoxia/reoxygenation rat astrocytes." dans: Journal of ethnopharmacology, Vol. 150, Issue 1, pp. 100-7, (2013) (PubMed).

    Yang, Zhou, Gao, Chen, Tu, Sun, Liu, He, Liu, Yuan: "Neuroprotective effects of bone marrow stem cells overexpressing glial cell line-derived neurotrophic factor on rats with intracerebral hemorrhage and neurons exposed to hypoxia/reoxygenation." dans: Neurosurgery, Vol. 68, Issue 3, pp. 691-704, (2011) (PubMed).

  • Antigène Voir toutes GDNF Kits ELISA

    GDNF (Glial Cell Line Derived Neurotrophic Factor (GDNF))

    Autre désignation

    GDNF

    Sujet

    Protein Function: Neurotrophic factor that enhances survival and morphological differentiation of dopaminergic neurons and increases their high-affinity dopamine uptake. .

    Background: Glial cell line-derived neurotrophic factor(GDNF) is a glycosylated, disulfide-bonded homodimer that is a distantly related member of the transforming growth factor-beta superfamily. GDNF, is a potent neurotrophic factor that promotes the survival of dopaminergic neurones in cultures including embryonic neuronal cultures. GDNF, in addition to its potential role in the differentiation and survival of central nervous system neurons, has profound effects on kidney organogenesis and the development of the peripheral nervous system.3 GDNF may have utility in the treatment of Parkinson's disease, which is marked by progressive degeneration of midbrain dopaminergic neurons. GDNF lies on the short arm of human chromosome 5, at 5p13.1-p13.3 ability to promote dopamine uptake in midbrain cultures. The standard product used in this kit is recombinant rat GDNF, which is a dimmer composed of two chains with 134 amino acids.

    Synonyms: Glial cell line-derived neurotrophic factor ,Gdnf ,

    Full Gene Name: Glial cell line-derived neurotrophic factor

    Cellular Localisation: Secreted.

    ID gène

    25453

    UniProt

    A7UGJ1

    Pathways

    Signalisation RTK, Synaptic Membrane, Tube Formation, Autophagy, Smooth Muscle Cell Migration
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