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SLC22A5 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement SLC22A5 dans IHC. Il présente une réactivité envers Humain, Rat et Souris.
N° du produit ABIN7258130

Aperçu rapide pour SLC22A5 anticorps (ABIN7258130)

Antigène

Voir toutes SLC22A5 Anticorps
SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

Reactivité

  • 25
  • 16
  • 13
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain, Rat, Souris

Hôte

  • 26
Lapin

Clonalité

  • 26
Polyclonal

Conjugué

  • 16
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SLC22A5 est non-conjugé

Application

  • 15
  • 11
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human SLC22A5

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    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

    SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

    Autre désignation

    SLC22A5

    Sujet

    Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants.

    ID gène

    6584

    UniProt

    O76082
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