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UGT1A1 anticorps (Middle Region)

L’anticorps Lapin Polyclonal anti-UGT1A1 a été validé pour WB. Il convient pour détecter UGT1A1 dans des échantillons de Humain, Rat, Souris, Cheval, Boeuf (Vache), Porc, Lapin et Mouton.
N° du produit ABIN2781805

Aperçu rapide pour UGT1A1 anticorps (Middle Region) (ABIN2781805)

Antigène

Voir toutes UGT1A1 Anticorps
UGT1A1 (UDP Glucuronosyltransferase 1 Family, Polypeptide A1 (UGT1A1))

Reactivité

Humain, Rat, Souris, Cheval, Boeuf (Vache), Porc, Lapin, Mouton

Hôte

  • 39
  • 4
  • 1
Lapin

Clonalité

  • 40
  • 4
Polyclonal

Conjugué

  • 23
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp UGT1A1 est non-conjugé

Application

  • 26
  • 21
  • 16
  • 15
  • 13
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
Western Blotting (WB)
  • Épitope

    • 8
    • 6
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    Séquence

    ASVWLFRSDF VKDYPRPIMP NMVFVGGINC LHQNPLSQEF EAYINASGEH

    Homologie

    Cow: 86%, Horse: 86%, Human: 100%, Mouse: 93%, Pig: 86%, Rabbit: 86%, Rat: 86%, Sheep: 86%

    Attributs du produit

    This is a rabbit polyclonal antibody against UGT1A1. It was validated on Western Blot using a cell lysate as a positive control.

    Purification

    Protein A purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the middle region of human UGT1A1
  • Indications d'application

    Optimal working dilutions should be determined experimentally by the investigator.

    Commentaires

    Antigen size: 533 AA

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    Lot specific

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Antigène

    UGT1A1 (UDP Glucuronosyltransferase 1 Family, Polypeptide A1 (UGT1A1))

    Autre désignation

    UGT1A1

    Sujet

    UGT1A1 is a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. The preferred substrate of this enzyme is bilirubin, although it also has moderate activity with simple phenols, flavones, and C18 steroids.This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The preferred substrate of this enzyme is bilirubin, although it also has moderate activity with simple phenols, flavones, and C18 steroids. Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome.
    Alias Symbols: GNT1, HUG-BR1, UDPGT, UGT1, UGT1A, BILIQTL1, UDPGT 1-1
    Protein Interaction Partner: COPZ1, SEC23B, UGDH, B3GALT1,
    Protein Size: 533

    Poids moléculaire

    57 kDa

    ID gène

    54658

    NCBI Accession

    NM_000463, NP_000454

    UniProt

    P22309

    Pathways

    Steroid Hormone Biosynthesis, Regulation of Lipid Metabolism by PPARalpha
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