8 results for "SLC26A4" in Products

SLC26A4 Products

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. [provided by RefSeq]

Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC
Immunohistochemistry-Paraffin: SLC26A4 Antibody [NBP1-85237]
(5)
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC, WB
Western Blot: SLC26A4 Antibody [NBP1-60106]
(2)
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Reactivity: Human
Source: Wheat germ
Applications: WB, ELISA, AP, MA, PAGE
SDS-PAGE: Recombinant Human SLC26A4 GST (N-Term) Protein [H00005172-P01]
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Reactivity: Mouse
Details: Rabbit Polyclonal
Applications: WB
Western Blot: SLC26A4 Antibody [NBP2-88291]
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Reactivity: Human
Sensitivity: 0.121 ng/mL (example only; lot dependent)
Assay Range: 0.312 - 20 ng/mL (example only; lot dependent)
Applications: ELISA
Human SLC26A4 - Ready-To-Use ELISA Kit (Colorimetric)
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Reactivity: Human
Sensitivity: 0.121 ng/mL (example only; lot dependent)
Assay Range: 0.312 - 20 ng/mL (example only; lot dependent)
Applications: ELISA
Human SLC26A4 ELISA Kit (Colorimetric)
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Reactivity: Human
Details: Mouse IgG2a Kappa Monoclonal Clone #3D2
Applications: ELISA
ELISA: SLC26A4 Antibody (3D2) [H00005172-M03]
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Reactivity: Human
Source: E. coli
Applications: AC
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