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SLC29A3 anticorps (AA 1-110)

Cet anticorps Lapin Polyclonal détecte spécifiquement SLC29A3 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN6147951

Aperçu rapide pour SLC29A3 anticorps (AA 1-110) (ABIN6147951)

Antigène

Voir toutes SLC29A3 Anticorps
SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

Reactivité

  • 14
  • 5
  • 5
  • 3
  • 3
Humain

Hôte

  • 15
Lapin

Clonalité

  • 15
Polyclonal

Conjugué

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
Cet anticorp SLC29A3 est non-conjugé

Application

  • 15
  • 10
  • 10
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 1-110

    Séquence

    MAVVSEDDFQ HSSNSTYRTT SSSLRADQEA LLEKLLDRPP PGLQRPEDRF CGTYIIFFSL GIGSLLPWNF FITAKEYWMF KLRNSSSPAT GEDPEGSDIL NYFESYLAVA

     Réactivité croisée

    Humain

    Attributs du produit

    Polyclonal Antibodies

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-110 of human SLC29A3 (NP_060814.4).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Commentaires

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    SLC29A3 (Solute Carrier Family 29 Member 3 (SLC29A3))

    Autre désignation

    SLC29A3

    Sujet

    This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.,SLC29A3,ENT3,HCLAP,HJCD,PHID,SLC29A3

    Poids moléculaire

    35 kDa/51 kDa

    ID gène

    55315

    UniProt

    Q9BZD2
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