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C8ORF37 Protein (His tag)

C8ORF37 Spezies: Human Wirt: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN5505604
  • Target Alle C8ORF37 Produkte
    C8ORF37 (Chromosome 8 Open Reading Frame 37 (C8ORF37))
    Protein-Typ
    Recombinant
    Spezies
    Human
    Quelle
    • 1
    Escherichia coli (E. coli)
    Aufreinigungstag / Konjugat
    Dieses C8ORF37 Protein ist gelabelt mit His tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Purified recombinant protein of Human chromosome 8 open reading frame 37 (C8orf37), full length, with N-terminal HIS tag, expressed in E. coli, 50 μg (full length, N-term HIS tag) protein expressed in E.coli.
    • Produced with end-sequenced ORF clone
    Aufreinigung
    Purified
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the N-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    C8ORF37 (Chromosome 8 Open Reading Frame 37 (C8ORF37))
    Andere Bezeichnung
    chromosome 8 open reading frame 37 (C8ORF37 Produkte)
    Synonyme
    CORD16 Protein, RP64 Protein, smalltalk Protein, chromosome 8 open reading frame 37 Protein, C8orf37 Protein
    Hintergrund
    This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP).
    Molekulargewicht
    23.2 kDa
    NCBI Accession
    NP_808880
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