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4 results for "SLC26A4 Antibodies" in Products
SLC26A4 Antibodies
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq]
| Reactivity: | Human |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, WB |
![Western Blot: SLC26A4 Antibody [NBP1-60106]](https://resources.rndsystems.com/images/products/SLC26A4-Antibody-Western-Blot-NBP1-60106-img0004.jpg "Western Blot: SLC26A4 Antibody [NBP1-60106]")
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| Reactivity: | Human |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC |
![Immunohistochemistry-Paraffin: SLC26A4 Antibody [NBP1-85237]](https://resources.rndsystems.com/images/products/SLC26A4-Antibody-Immunohistochemistry-Paraffin-NBP1-85237-img0009.jpg "Immunohistochemistry-Paraffin: SLC26A4 Antibody [NBP1-85237]")
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| Reactivity: | Mouse |
| Details: | Rabbit Polyclonal |
| Applications: | WB |
![Western Blot: SLC26A4 Antibody [NBP2-88291]](https://resources.rndsystems.com/images/products/SLC26A4-Antibody-Western-Blot-NBP2-88291-img0001.jpg "Western Blot: SLC26A4 Antibody [NBP2-88291]")
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| Reactivity: | Human |
| Details: | Mouse IgG2a Kappa Monoclonal Clone #3D2 |
| Applications: | ELISA |
![ELISA: SLC26A4 Antibody (3D2) [H00005172-M03]](https://resources.rndsystems.com/images/products/SLC26A4-Antibody-3D2-ELISA-H00005172-M03-img0001.jpg "ELISA: SLC26A4 Antibody (3D2) [H00005172-M03]")
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