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FBLN4 anticorps (AA 331-443) (Biotin)

FBLN4 Reactivité: Humain WB, ELISA, IHC (p), IHC (fro) Hôte: Lapin Polyclonal Biotin
N° du produit ABIN1701235
  • Antigène Voir toutes FBLN4 Anticorps
    FBLN4 (Fibulin 4 (FBLN4))
    Épitope
    • 14
    • 9
    • 8
    • 7
    • 6
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 331-443
    Reactivité
    • 63
    • 22
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 61
    • 3
    Lapin
    Clonalité
    • 63
    • 1
    Polyclonal
    Conjugué
    • 30
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FBLN4 est conjugé à/à la Biotin
    Application
    • 53
    • 27
    • 26
    • 15
    • 13
    • 13
    • 7
    • 6
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Homologie
    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human EFEMP2/Fibulin 4
    Isotype
    IgG
    Top Product
    Discover our top product FBLN4 Anticorps primaire
  • Indications d'application
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C for 12 months.
    Date de péremption
    12 months
  • Dekker, van Geemen, van den Bogaerdt, Driessen-Mol, Aikawa, Smits: "Sheep-Specific Immunohistochemical Panel for the Evaluation of Regenerative and Inflammatory Processes in Tissue-Engineered Heart Valves." dans: Frontiers in cardiovascular medicine, Vol. 5, pp. 105, (2018) (PubMed).

  • Antigène
    FBLN4 (Fibulin 4 (FBLN4))
    Autre désignation
    EFEMP2/Fibulin 4 (FBLN4 Produits)
    Synonymes
    anticorps CB257, anticorps fbln4, anticorps fc56c09, anticorps id:ibd2923, anticorps sb:cb257, anticorps wu:fc56c09.x1, anticorps ARCL1B, anticorps FBLN4, anticorps MBP1, anticorps UPH1, anticorps 0610011K11Rik, anticorps Fbln4, anticorps FIBL-4, anticorps Fibulin-4, anticorps H411, anticorps EGF-containing fibulin-like extracellular matrix protein 2, anticorps EGF containing fibulin-like extracellular matrix protein 2b, anticorps fibulin 4, anticorps EGF containing fibulin like extracellular matrix protein 2, anticorps epidermal growth factor-containing fibulin-like extracellular matrix protein 2, anticorps Efemp2, anticorps efemp2b, anticorps fbln4, anticorps EFEMP2
    Sujet

    Synonyms: EFEMP2, EGF containing fibulin like extracellular matrix protein 2, EGF-containing fibulin-like extracellular matrix protein 2, FBLN 4, FBLN4, FBLN4_HUMAN, FIBL 4, FIBL-4, FIBL4, Fibulin4, Fibulin-4, MBP 1, MBP1, Mutant p53 binding protein 1, Protein UPH1, UPH 1, UPH1, UPH1 protein.

    Background: Fibulin proteins contribute to normal development of elastic fiber systems in various types of organs that require elasticity, such as vasculature, lung and skin. Fibulin-4, also known as EFEMP2 (EGF-containing fibulin-like extracellular matrix protein 2), MBP1 or UPH1 is a 443 amino acid secreted protein that contains six EGF-like calcium-binding domains and belongs to the fibulin family. Expressed ubiquitously with highest expression in heart, Fibulin-4 is essential for connective tissue development and elastic fiber formation, and may also play an important role in vascular patterning and collagen biosynthesis. Defects in the gene encoding Fibulin-4 are associated with autosomal recessive cutis laxa type I (CL type I), a connective tissue disorder that is inherited in both an autosomal dominant and an autosomal recessive manner and is characterized by inelastic tissue in all affected areas of the body.

    ID gène
    30008
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