Solute Carrier Family 16 Member 2 (SLC16A2) Antibody
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Description
Rabbit polyclonal antibody against SLC16A2 protein. Immunogen region is Internal.
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Solute Carrier Family 16 Member 2 (SLC16A2) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1/500 - 1/3000, ELISA: 1/40000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen. |
| Size 1 | 10 µg |
| Size 2 | 100 µg |
| Size 3 | 200 µg |
| Size 4 | 300 µg |
| Size 5 | 1 mg |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS (without Mg<sup>2+</sup> and Ca<sup>2+</sup>), pH 7.4, 150 mM NaCl, 0.02% sodium azide, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P36021 |
| Background | Antibody anti-SLC16A2 |
| Status | RUO |
| Note | Concentration: 1 mg/ml - |
Descripción
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SLC16A2 antibody
Very active and specific thyroid hormone transporter. Stimulates cellular uptake of thyroxine(T4), triiodothyronine(T3), reverse triiodothyronine(rT3) and diidothyronine. Does not transport Leu, Phe, Trp or Tyr.
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Solute Carrier Family 16 Member 2 (SLC16A2) Antibody
SLC16A2 Antibody is a Rabbit Polyclonal antibody against SLC16A2. This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome.
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Solute Carrier Family 16 Member 2 (SLC16A2) Antibody
Rabbit polyclonal antibody against SLC16A2 protein. Immunogen region is Internal.
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