Thermo Fisher Scientific SLC22A4 Polyclonal Antibody
Rabbit polyclonal antibody targeting human SLC22A4 recombinant protein. Unconjugated, liquid form with 0.05 mg/mL concentration. Suitable for research use in carnitine transporter studies. Store at 4°C short term or -20°C long term.
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Product Specifications
| 항목 | 내용 |
|---|---|
| Host/Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human SLC22A4 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.05 mg/mL |
| Storage Conditions | Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2790521 |
Product Specific Information
Immunogen sequence: SLGMTLPETL EQMQKVKWFR SGKKTRDSME TEENPKVLIT AF
Target Information
Carnitine (b-hydroxy-g-trimethylaminobutyrate) is a small, highly polar compound that aids in the β-oxidation of long-chain fatty acids. Organic cation/carnitine transporters (OCTN) assist in the elimination of cationic compounds, including xenobiotics, and transport carnitine for reabsorption in the kidney. Similar to organic cation transporters (OCT), OCTN proteins localize to the plasma membrane of epithelial cells.
- OCTN1 is expressed in kidney, trachea, bone marrow, and fetal liver.
- OCTN2 is abundantly expressed in kidney, skeletal muscle, placenta, and heart.
- OCTN3 is strongly expressed in testis and weakly expressed in kidney.
The gene encoding human OCTN1 maps to chromosome 5, and the gene encoding human OCTN2 maps to chromosome 5q31. Mutations in the gene encoding OCTN2 lead to systemic carnitine deficiency (SCD), an autosomal recessive disorder characterized by cardiomyopathy, skeletal myopathy, lethargy, hypoglycemia, and hyperammonemia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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