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PHYH Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

PHYH Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2728871
  • Target See all PHYH Proteins
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant 1
    Origin
    • 3
    • 1
    • 1
    • 1
    Human
    Source
    • 2
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This PHYH protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human PHYH / PAHX (transcript variant 1) 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 PHYH 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
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Alternative Name
    Phyh,pahx (PHYH Products)
    Synonyms
    zgc:110203 Protein, LN1 Protein, LNAP1 Protein, PAHX Protein, PHYH1 Protein, RD Protein, AI256161 Protein, AI265699 Protein, Lnap1 Protein, phytanoyl-CoA 2-hydroxylase Protein, phytanoyl-CoA hydroxylase-like Protein, phytanoyl-CoA hydroxylase Protein, PHYH Protein, LOC478001 Protein, phyh Protein, Phyh Protein
    Background
    This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
    Molecular Weight
    35.4 kDa
    NCBI Accession
    NP_006205
    Pathways
    Monocarboxylic Acid Catabolic Process
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