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PMPCA Protein (Myc-DYKDDDDK Tag)

PMPCA Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2729218
  • Target See all PMPCA products
    PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This PMPCA protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human PMPCA 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
    PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
    Alternative Name
    Pmpca (PMPCA Products)
    Synonyms
    Alpha-MPP Protein, INPP5E Protein, 1200002L24Rik Protein, 4933435E07Rik Protein, P-55 Protein, wu:fi19e06 Protein, wu:fj83d11 Protein, zgc:101647 Protein, MGC114896 Protein, DKFZp459H0315 Protein, peptidase, mitochondrial processing alpha subunit Protein, peptidase (mitochondrial processing) alpha Protein, peptidase (mitochondrial processing) alpha S homeolog Protein, PMPCA Protein, Pmpca Protein, pmpca Protein, pmpca.S Protein
    Background
    The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2.
    Molecular Weight
    58.1 kDa
    NCBI Accession
    NP_055975
    Pathways
    Inositol Metabolic Process, SARS-CoV-2 Protein Interactome
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