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Invitrogen™ SLC26A4 Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5115911
This item is not returnable.
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Description
Antibody detects endogenous levels of total SLC26A4.
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.
Specifications
| SLC26A4 | |
| Polyclonal | |
| Unconjugated | |
| SLC26A4 | |
| DFNB4; EVA; PDS; Pendred syndrome homolog; Pendred's syndrome; pendrin; Slc26a4; Sodium-independent chloride/iodide transporter; solute carrier family 26 (anion exchanger), member 4; solute carrier family 26 member 4; solute carrier family 26, member 4; TDH2B; truncated solute carrier family 26 | |
| Rabbit | |
| Affinity chromatography | |
| RUO | |
| 23985, 29440, 5172 | |
| -20°C | |
| Liquid |
| Western Blot, Immunocytochemistry | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide | |
| O43511, Q9R154, Q9R155 | |
| SLC26A4 | |
| A synthesized peptide derived from human SLC26A4(Accession O43511), corresponding to amino acid residues L498-L548. | |
| 100 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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