Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

PHYH Protein

Recombinant PHYH-Protein exprimiert in Escherichia coli (E. coli).
Produktnummer ABIN7317253

Kurzübersicht für PHYH Protein (ABIN7317253)

Target

Alle PHYH Proteine anzeigen
PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))

Protein-Typ

Recombinant

Spezies

  • 4
  • 1
  • 1
Human

Quelle

  • 2
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Reinheit

> 80 % as determined by reducing SDS-PAGE.
  • Verwendungszweck

    Recombinant Human PHYH Protein

    Sequenz

    Ser31-Leu338

    Produktmerkmale

    A DNA sequence encoding the human PHYH (O14832) (Ser31-Leu338) was expressed, with a N-terminal Met.
  • Möchten Sie weitere Optionen für dieses Protein ?

    !
    Entdecken Sie unsere vordefinierten maßgeschneiderten Proteine und Proteinservices!

    Ihr Projekt erfordert weitere Anpassungen? Kontaktieren Sie uns und entdecken Sie unsere maßgeschneiderten Proteinlösungen

  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from sterile 20 mM mops, 10 % glycerol, 2 mM DDT, 1 mM EDTA, 0.2 mM PMSF, 0.2M NaCl, pH 7.2

    Lagerung

    4 °C,-20 °C,-80 °C

    Informationen zur Lagerung

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Target

    PHYH (Phytanoyl-CoA 2-Hydroxylase (PHYH))

    Andere Bezeichnung

    PHYH

    Hintergrund

    Background: PHYH belongs to the family of iron(II)-dependent oxygenases, which typically incorporate one atom of dioxygen into the substrate and one atom into the succinate carboxylate group. PHYH is expressed in liver, kidney, and T-cells, but not in spleen, brain, heart, lung and skeletal muscle. It converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Defects in PHYH can cause Refsum disease (RD). RD is an autosomal recessive disorder characterized clinically by a tetrad of abnormalities: retinitis pigmentosa, peripheral neuropathy, cerebellar ataxia, and elevated protein levels in the cerebrospinal fluid (CSF). Patients exhibit accumulation of the branched-chain fatty acid, phytanic acid, in blood and tissues.

    Synonym: LN1,LNAP1,PAHX,PHYH1,RD

    Molekulargewicht

    35.6 kDa

    UniProt

    O14832

    Pathways

    Monocarboxylic Acid Catabolic Process
Sie sind hier:
Chat with us!