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OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

OPA1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2727921
  • Target See all OPA1 Proteins
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 3
    Origin
    • 6
    • 3
    Human
    Source
    • 6
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This OPA1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Optic atrophy 1 (autosomal dominant) (OPA1), nuclear gene encoding mitochondrial protein, transcript variant 3 (transcript variant 3) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product OPA1 Protein
  • 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
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    Abstract
    OPA1 Products
    Synonyms
    1200011N24Rik Protein, AI225888 Protein, AI847218 Protein, lilr3 Protein, mKIAA0567 Protein, MGM1 Protein, NPG Protein, NTG Protein, largeG Protein, fk62d06 Protein, wu:fb77a10 Protein, wu:fk62d06 Protein, zgc:92092 Protein, OPA1, mitochondrial dynamin like GTPase Protein, optic atrophy 1 (autosomal dominant) Protein, Opa1 Protein, OPA1 Protein, opa1 Protein
    Background
    This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene.
    Molecular Weight
    109.2 kDa
    NCBI Accession
    NP_570845
    Pathways
    Tube Formation
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