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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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