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Invitrogen™ SLC26A4 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA560149
Description
Immunogen sequence: FGLLTVVLRV QFPSWNGLGS IPSTDIYKST KNYKNIEEPQ GVKILRFSSP IFYGNVDGFK KCIKSTVGFD AIRVYNKRLK ALRK Highest antigen sequence identity to the following orthologs: Mouse - 89%, Rat - 90%.
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 | |
Antigen affinity chromatography | |
RUO | |
5172 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry (Paraffin) | |
0.10 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
O43511 | |
SLC26A4 | |
Recombinant protein corresponding to Human SLC26A4. Recombinant protein control fragment (Product #RP-92645). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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