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C12orf53 Protein (Fc Tag)

C12orf53 Spezies: Human Wirt: HEK-293 Cells Recombinant > 96 % as determined by reducing SDS-PAGE.
Produktnummer ABIN7317278
  • Target Alle C12orf53 Proteine anzeigen
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 2
    Human
    Quelle
    • 4
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses C12orf53 Protein ist gelabelt mit Fc Tag.
    Verwendungszweck
    Recombinant Human C12orf53 Protein (Fc Tag)
    Sequenz
    Met 1-Pro178
    Produktmerkmale
    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.
    Reinheit
    > 96 % as determined by reducing SDS-PAGE.
    Endotoxin-Niveau
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product C12orf53 Protein
  • Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from sterile PBS, pH 7.4
    Lagerung
    4 °C,-20 °C,-80 °C
    Informationen zur Lagerung
    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.
  • Target
    C12orf53 (Chromosome 12 Open Reading Frame 53 (C12orf53))
    Andere Bezeichnung
    C12orf53 (C12orf53 Produkte)
    Synonyme
    C12orf53 Protein, PANP Protein, leda-1 Protein, PILR alpha associated neural protein Protein, PIANP Protein
    Hintergrund

    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

    Molekulargewicht
    42.3 kDa
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