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Invitrogen™ SLC26A4 Polyclonal Antibody
GREENER_CHOICE

Rabbit Polyclonal Antibody

Brand:  Invitrogen™ PA5115911

Product Code. 17238693

  • £455.00 / 100µL

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Description

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.
TRUSTED_SUSTAINABILITY
Specifications

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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