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FAM36A Protein (Myc-DYKDDDDK Tag)

FAM36A Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2720778
  • Target See all FAM36A products
    FAM36A (Family with Sequence Similarity 36, Member A (FAM36A))
    Protein Type
    Recombinant
    Origin
    • 1
    • 1
    Human
    Source
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This FAM36A protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human FAM36A protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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))
    Alternative Name
    Fam36a (FAM36A Products)
    Synonyms
    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
    Background
    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.
    Molecular Weight
    13.1 kDa
    NCBI Accession
    NP_932342
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