SLC22A5 anticorps

N° du produit ABIN7009509

Détail du produit anti-SLC22A5 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC22A5 est non-conjugé

Application: Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: IF 1:50-1:200

Restrictions: For Research Use only

Stockage

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.

Détails sur SLC22A5

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

Autre désignation: SLC22A5 (SLC22A5 Produits)

Synonymes: anticorps CDSP, anticorps OCTN2, anticorps OCTN2VT, anticorps Lstpl, anticorps Octn2, anticorps jvs, anticorps slc22a5, anticorps MGC68932, anticorps CT1, anticorps UST2r, anticorps ATOCT2, anticorps OCT2, anticorps ORGANIC CATION TRANSPORTER 2, anticorps YUP8H12R.2, anticorps YUP8H12R_2, anticorps organic cation/carnitine transporter 2, anticorps solute carrier family 22 member 5, anticorps solute carrier family 22 (organic cation transporter), member 5, anticorps solute carrier family 22 member 5 L homeolog, anticorps organic cation/carnitine transporter 2, anticorps SLC22A5, anticorps Slc22a5, anticorps LOC100358417, anticorps slc22a5.L, anticorps OCT2

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