SLC22A5 antibody
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | solute carrier family 22(organic cation/carnitine transporter), member 5 (SLC22A5) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500-1:1000; IHC: 1:20-1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 75 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| UniProt ID | O76082 |
| Alias | Organic cation/carnitine transporter 2,High-affinity sodium-dependent carnitine cotransporter,Solute carrier family 22 member 5,SLC22A5,OCTN2 |
| Background | Antibody anti-SLC22A5 |
| Status | RUO |
| Note | Mol. Weight 75 kDa |
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SLC22A5 Antibody is a Rabbit Polyclonal antibody against SLC22A5. 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. [provided by RefSeq, Jul 2008].
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