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FAM36A Protein (Myc-DYKDDDDK Tag)

FAM36A Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2720778
  • Target Alle FAM36A Produkte
    FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
    Protein-Typ
    Recombinant
    Spezies
    • 1
    • 1
    Human
    Quelle
    • 2
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses FAM36A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human FAM36A protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    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 C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    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
    FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
    Andere Bezeichnung
    Fam36a (FAM36A Produkte)
    Synonyme
    FAM36A Protein, 2310005N03Rik Protein, Fam36a Protein, RGD1309105 Protein, cox20 Protein, fam36a Protein, COX20, cytochrome c oxidase assembly factor Protein, COX20 Cox2 chaperone Protein, COX20 cytochrome C oxidase assembly factor Protein, COX20 cytochrome c oxidase assembly factor L homeolog Protein, COX20 Protein, Cox20 Protein, cox20.L Protein
    Hintergrund
    This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants.
    Molekulargewicht
    13.1 kDa
    NCBI Accession
    NP_932342
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