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HMBS Protein (His tag)

Cette protéine Recombinant HMBS est exprimée dans Human Cells.
N° du produit ABIN7318923

Aperçu rapide pour HMBS Protein (His tag) (ABIN7318923)

Antigène

Voir toutes HMBS Protéines
HMBS (Hydroxymethylbilane Synthase (HMBS))

Type de proteíne

Recombinant

Origine

  • 8
  • 1
  • 1
Humain

Source

  • 4
  • 2
  • 2
  • 1
  • 1
Human Cells

Pureté

> 95 % as determined by reducing SDS-PAGE.
  • Purification/Conjugué

    Cette HMBS protéine est marqué à la His tag.

    Fonction

    Recombinant Human HMBS Protein (His Tag)

    Séquence

    Ser2-His361

    Attributs du produit

    Recombinant Human Porphobilinogen Deaminase is produced by our Mammalian expression system and the target gene encoding Ser2-His361 is expressed with a 6His tag at the C-terminus.

    niveau d'endotoxine

    < 1.0 EU per μg as determined by the LAL method.
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  • Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Please refer to the printed manual for detailed information.

    Buffer

    Lyophilized from a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.

    Stock

    4 °C,-20 °C,-80 °C

    Stockage commentaire

    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.
  • Antigène

    HMBS (Hydroxymethylbilane Synthase (HMBS))

    Autre désignation

    HMBS

    Sujet

    Background: Porphobilinogen Deaminase (HMBS) is a member of the HMBS family. PBGD is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. HMBS is involved in the production of heme, which is important for all of the body's organs, although it is most abundant in the blood, bone marrow, and liver. In addition, Heme is an essential component of iron-containing proteins called hemoproteins, including hemoglobin. Defects in PBGD are the cause of acute intermittent porphyria.

    Synonym: Porphobilinogen Deaminase, PBG-D, Hydroxymethylbilane Synthase, HMBS, Pre-Uroporphyrinogen Synthase, HMBS, PBGD, UPS

    Poids moléculaire

    40.5 kDa

    UniProt

    P08397
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