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FAM36A Protein (Myc-DYKDDDDK Tag)

FAM36A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2720778
  • Antigène Tous les produits FAM36A
    FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette FAM36A protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human FAM36A protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    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.
  • Antigène
    FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
    Autre désignation
    Fam36a (FAM36A Produits)
    Synonymes
    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
    Sujet
    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.
    Poids moléculaire
    13.1 kDa
    NCBI Accession
    NP_932342
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