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Phytanoyl-CoA 2-Hydroxylase (PHYH) (N-Term) Peptid

PHYH Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN981712
  • Target Alle PHYH Produkte
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Protein Region
    N-Term
    Spezies
    Human
    Quelle
    • 4
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    TLPEILKYVE CFTGPNIMAM HTMLINKPPD SGKKTSRHPL HQDLHYFPFR
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-PHYH Antibody(ARP56681_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))
    Synonyme
    zgc:110203 Peptide, LN1 Peptide, LNAP1 Peptide, PAHX Peptide, PHYH1 Peptide, RD Peptide, AI256161 Peptide, AI265699 Peptide, Lnap1 Peptide, phytanoyl-CoA 2-hydroxylase Peptide, phytanoyl-CoA hydroxylase-like Peptide, phytanoyl-CoA hydroxylase Peptide, PHYH Peptide, LOC478001 Peptide, phyh Peptide, Phyh Peptide
    Hintergrund
    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.

    Alias Symbols: LN1, LNAP1, PAHX, PHYH1, RD

    Protein Interaction Partner: ACSL6,F8,FKBP4,MAGEA11,PEX7,PHYH,PHYHIP,TOM1L1,COPS3,F8,FKBP4,MAGEA11,PEX7,TOM1L1,WDR8

    Protein Size: 238
    Molekulargewicht
    26 kDa
    Gen-ID
    5264
    NCBI Accession
    NM_001037537, NP_001032626
    UniProt
    O14832
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