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MFAP4 Protein (His tag)

MFAP4 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS
N° du produit ABIN1098675
  • Antigène Voir toutes MFAP4 Protéines
    MFAP4 (Microfibrillar-Associated Protein 4 (MFAP4))
    Type de proteíne
    Recombinant
    Origine
    • 9
    • 2
    • 2
    • 1
    • 1
    Humain
    Source
    • 5
    • 3
    • 2
    • 2
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette MFAP4 protéine est marqué à la His tag.
    Application
    SDS-PAGE (SDS)
    Pureté
    > 90 % by SDS - PAGE
    Top Product
    Discover our top product MFAP4 Protéine
  • Commentaires

    Synonyms: microfibrillar-associated protein 4, Microfibril associated glycoprotein 4, Microfibril-associated glycoprotein 4

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/ml (determined by Bradford assay)
    Buffer
    20 mM Tris-HCl buffer (pH 8.0) containing 0.4 M UREA, 10% glycerol
    Stock
    4 °C
    Stockage commentaire
    Avoid repeated freezing and thawing cycles.
  • Antigène
    MFAP4 (Microfibrillar-Associated Protein 4 (MFAP4))
    Autre désignation
    MFAP4 (MFAP4 Produits)
    Synonymes
    1110007F23Rik Protein, Magp-36 Protein, zgc:77076 Protein, microfibril-associated glycoprotein 4 Protein, microfibrillar-associated protein 4 Protein, microfibril associated protein 4 S homeolog Protein, microfibril associated protein 4 Protein, CpipJ_CPIJ000434 Protein, CpipJ_CPIJ006120 Protein, CpipJ_CPIJ010089 Protein, CpipJ_CPIJ018551 Protein, CpipJ_CPIJ020296 Protein, mfap4 Protein, mfap4.S Protein, MFAP4 Protein, Mfap4 Protein
    Sujet
    MFAP4, also as known as microfibrillar-associated protein 4, belongs to Fibrinogen protein family and contains 1 fibrinogen C-terminal domain. This protein has similarity to a bovine microfibril-associated protein. The protein has binding specificities for both collagen and carbohydrate. It is thought to be an extracellular matrix protein which is involved in cell adhesion or intercellular interactions. Deletion of MFAP4 was found in 30 of 31 patients with Smith-Magenis syndrome (SMS), a clinically recognizable multiple congenital anomaly/mental retardation syndrome. Recombinant human MFAP4 protein, fused to His-tag at N-terminus, was expressed in E.coli.
    Poids moléculaire
    29.2 kDa (259aa)
    NCBI Accession
    NP_002395
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