SLC22A5 anticorps (AA 1-180)

N° du produit ABIN3022379

Cet anticorps anti-SLC22A5 est un anticorps Lapin Polyclonal détectant SLC22A5 dans WB. Adapté pour Humain.

Aperçu rapide pour SLC22A5 anticorps (AA 1-180) (ABIN3022379)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC22A5 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SLC22A5 anticorps

Épitope: AA 1-180

Séquence: MRDYDEVTAF LGEWGPFQRL IFFLLSASII PNGFTGLSSV FLIATPEHRC RVPDAANLSS AWRNHTVPLR LRDGREVPHS CRRYRLATIA NFSALGLEPG RDVDLGQLEQ ESCLDGWEFS QDVYLSTIVT EWNLVCEDDW KAPLTISLFF VGVLLGSFIS GQLSDRFGRK NVLFVTMGMQ

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human SLC22A5 (NP_003051.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

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.

Conseil sur la manipulation: Avoid freeze / thaw cycles

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

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.,SLC22A5,CDSP,OCTN2,Cancer,Signal Transduction,Endocrine & Metabolism,SLC22A5

Poids moléculaire: 24 kDa/62 kDa/65 kDa

ID gène: 6584

UniProt: O76082