Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

SLC22A5 anticorps

L’anticorps Lapin Polyclonal anti-SLC22A5 a été validé pour IF. Il convient pour détecter SLC22A5 dans des échantillons de Humain, Rat et Souris.
N° du produit ABIN6568843

Aperçu rapide pour SLC22A5 anticorps (ABIN6568843)

Antigène

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

Reactivité

  • 25
  • 17
  • 14
  • 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

  • 14
  • 10
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human SLC22A5 (NP_003051.1).

    Isotype

    IgG
  • Indications d'application

    IF 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.

    Poids moléculaire

    Observed_MW: 70kDa

    Calculated_MW: 24kDa/62kDa/65kDa

    ID gène

    6584

    UniProt

    O76082
Vous êtes ici:
Chat with us!