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DDHD2 Protein (His tag)

DDHD2 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN5505613
  • Target See all DDHD2 Proteins
    DDHD2 (DDHD Domain Containing 2 (DDHD2))
    Protein Type
    Recombinant
    Origin
    • 3
    • 1
    Human
    Source
    • 2
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This DDHD2 protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Purified recombinant protein of Human DDHD domain containing 2 (DDHD2), transcript variant 3, full length, with N-terminal HIS tag, expressed in E. coli, 50 μg (full length, N-term HIS tag, transcript variant 3) protein expressed in E.coli.
    • Produced with end-sequenced ORF clone
    Purification
    Purified
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product DDHD2 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 N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    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
    DDHD2 (DDHD Domain Containing 2 (DDHD2))
    Alternative Name
    DDHD domain containing 2 (DDHD2 Products)
    Synonyms
    SAMWD1 Protein, SPG54 Protein, 2010305K11Rik Protein, mKIAA0725 Protein, DDHD domain containing 2 Protein, DDHD2 Protein, Ddhd2 Protein, ddhd2 Protein
    Background
    This gene encodes a phospholipase enzyme containing sterile-alpha-motif (SAM), WWE, and DDHD domains. This protein participates in membrane trafficking between the endoplastic reticulum and the Golgi body. Mutations in this gene can cause autosomal recessive spastic paraplegia 54. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    25.8 kDa
    NCBI Accession
    NP_001157706
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