| 产品详情 |
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| Antigenic Specificity | Solute Carrier Family 26, Member 4 (SLC26A4) (Middle Region) |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human, mouse |
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| Isotype | n/a |
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| Format | affinity purified |
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| Size | 50 µg |
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| Concentration | n/a |
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| Applications | Western Blotting (WB) |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | 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. |
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| Immunogen | SLC26 A4 antibody was raised using the middle region of SLC26 4 corresponding to a region with amino acids ELNDRFRHKIPVPIPIEVIVTIIATAISYGANLEKNYNAGIVKSIPRGFL |
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| Other Names | Pds|DFNB4|EVA|PDS|TDH2B|pendrin |
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| Gene, Accession # | Gene ID: 5172,23985 |
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| Catalog # | ABIN635614 |
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| Price | |
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| Order / More Info | Solute Carrier Family 26, Member 4 (SLC26A4) (Middle Region) Antibody from ANTIBODIES-ONLINE GmbH |
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| Product Specific References | n/a |
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