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MTMR2 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

MTMR2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2726535
  • Target See all MTMR2 Proteins
    MTMR2 (Myotubularin Related Protein 2 (MTMR2))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 3
    Origin
    • 5
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This MTMR2 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human MTMR2 (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 MTMR2 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
    MTMR2 (Myotubularin Related Protein 2 (MTMR2))
    Alternative Name
    Mtmr2 (MTMR2 Products)
    Synonyms
    MTMR2 Protein, DKFZp459I198 Protein, CMT4B Protein, CMT4B1 Protein, 6030445P13Rik Protein, zgc:153915 Protein, myotubularin related protein 2 Protein, MTMR2 Protein, Mtmr2 Protein, mtmr2 Protein
    Background
    This gene is a member of the myotubularin family of phosphoinositide lipid phosphatases. The encoded protein possesses phosphatase activity towards phosphatidylinositol-3-phosphate and phosphatidylinositol-3,5-bisphosphate. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4B, an autosomal recessive demyelinating neuropathy. Alternatively spliced transcript variants encoding multiple isoforms have been found for this gene.
    Molecular Weight
    65.8 kDa
    NCBI Accession
    NP_958438
    Pathways
    Inositol Metabolic Process, Synaptic Membrane
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