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Invitrogen™ SLC26A4 Polyclonal Antibody

Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA542060
Description
Peptide sequence: ELNDRFRHKI PVPIPIEVIV TIIATAISYG ANLEKNYNAG IVKSIPRGFL Sequence homology: Cow: 92%; Dog: 100%; Guinea Pig: 100%; Horse: 93%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 92%.
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 | |
| 5172 | |
| -20°C, Avoid Freeze/Thaw Cycles | |
| Liquid |
| Western Blot | |
| 0.5 mg/mL | |
| PBS with 2% sucrose and 0.09% sodium azide | |
| O43511 | |
| SLC26A4 | |
| Synthetic peptide directed towards the middle region of human SLC26A4. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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