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C12orf53 Protein (Fc Tag)

C12orf53 Origine: Humain Hôte: HEK-293 Cells Recombinant > 96 % as determined by reducing SDS-PAGE.
N° du produit ABIN7317278
  • Antigène Voir toutes C12orf53 Protéines
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 2
    Humain
    Source
    • 4
    HEK-293 Cells
    Purification/Conjugué
    Cette C12orf53 protéine est marqué à la Fc Tag.
    Fonction
    Recombinant Human C12orf53 Protein (Fc Tag)
    Séquence
    Met 1-Pro178
    Attributs du produit
    A DNA sequence encoding the human C12orf53 (Q8IYJ0-1) (Met1-Pro178) was expressed, fused with the Fc region of human IgG1 at the C-terminus.
    Pureté
    > 96 % as determined by reducing SDS-PAGE.
    niveau d'endotoxine
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product C12orf53 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from sterile PBS, pH 7.4
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Antigène
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Autre désignation
    C12orf53 (C12orf53 Produits)
    Synonymes
    C12orf53 Protein, PANP Protein, leda-1 Protein, PILR alpha associated neural protein Protein, PIANP Protein
    Sujet

    Background: C12orf53 is mainly expressed in adult brain and cerebellum. It also can be detected in fetal brain and virtually no expression in spleen, heart, kidney, liver and dorsal ganglion relative to brain. C12orf53 acts as a ligand for PILRA in neural tissues, where it may be involved in immune regulation. Chromosome 12 encodes over 1,100 genes within 132 million bases. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC class I interaction.

    Synonym: C12orf53,leda-1,LEDA1,PANP,UNQ828/PRO1755

    Poids moléculaire
    42.3 kDa
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