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Invitrogen™ SLC26A4 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA542060

Catalog No. PIPA542060


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Description

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.
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
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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