产品名称 Solute Carrier Family 26, Member 4 (SLC26A4) (C-Term) Antibody from ANTIBODIES-ONLINE GmbH
产品货号 ABIN571494
产品价格 现货询价,电话:010-67529703
产品规格 100 µL
产品品牌 ANTIBODIES-ONLINE GmbH
产品概述
产品详情
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Antigenic SpecificitySolute Carrier Family 26, Member 4 (SLC26A4) (C-Term)
Clonepolyclonal
Host SpeciesRabbit
Reactive Specieshuman
Isotypen/a
Formatserum
Size100 µL
Concentrationn/a
ApplicationsImmunohistochemistry (IHC),Western Blotting (WB)
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DescriptionFunction: Sodium-independent transporter of chloride and iodide. Defects in SLC26A4 are a cause of Pendred syndrome (PDS). PDS is an autosomal recessive disorder characterized by congenital sensorineural hearing loss combined with thyroid goiter. The disorder may account for up to 10% of the cases of hereditary deafness. The deafness is most often associated with a Mondini cochlear defect. Defects in SLC26A4 are the cause of deafness autosomal recessive type 4 (DFNB4), also known as vestibular aqueduct syndrome (EVA). DFNB4 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNB4 is associated with an enlarged vestibular aqueduct.Tissue specificity: High expression in adult thyroid, lower expression in adult and fetal kidney and fetal brain. Not expressed in other tissues.Subcellular location: Membrane, Multi-pass membrane protein Also known as: Sodium-independent chloride/iodide transporter, Solute carrier family 26 member 4, SLC26A4, PDS.
ImmunogenA synthetic peptide from c-terminal region of human Pendrin (SLC26A4) conjugated to an immunogenic carrier protein was used as the antigen.
Other NamesPds|DFNB4|EVA|PDS|TDH2B|pendrin
Gene, Accession #Gene ID: 5172
Catalog #ABIN571494
Price
Order / More InfoSolute Carrier Family 26, Member 4 (SLC26A4) (C-Term) Antibody from ANTIBODIES-ONLINE GmbH
Product Specific Referencesn/a
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