Anti-Human SLC26A4 Polyclonal Antibody

Categories: [ Antibodies][ Polyclonal Antibodies]

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; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.

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Properties

Data Sheet	Click for Datasheet
Catalog Number	PA11034
Size	100μl
Host Type	Rabbit
Immunogen	Synthetic peptide of human SLC25A4
Specificity	High expression in adult thyroid, lower expression in adult and fetal kidney and fetal brain. Not expressed in other tissues.
Isotype	IgG
Reacitivity	Human
Clone
Uniprot	O43511
Concentration	0.5 mg/mL
Dilution	IHC 1:25-1:100
Formulation
Application	IHC,ELISA
Other Names	deafness,autosomal recessive 4,DFNB4,EVA,NSRD4,PDS,Pendred syndrome,Pendred syndrome homolog,Pendrin,S26A4,SLC26A4,Sodium independent chloride/iodide transporter,Sodium-independent chloride/iodide transporter,Solute carrier family 26 member 4
Storage	Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript	For research use only, not for use in diagnostic procedures.

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Anti-Human SLC26A4 Polyclonal Antibody

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