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USH1C Products

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive deafness.
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79 results for "USH1C" in Products

79 results for "USH1C" in Products

USH1C Products

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive deafness.
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Applications: IHC
Reactivity: Human, Mouse
Applications: IHC, WB, ICC/IF
Reactivity: Human, Mouse
Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: WB, ELISA
Reactivity: Human, Bovine
Applications: IHC, WB
Reactivity: Human
Applications: WB, ELISA, IP
Reactivity: Human
Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: WB, ELISA
Reactivity: Human
Applications: AC
Applications: WB
Applications: WB, ELISA
Reactivity: Human, Mouse, Rat
Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: ELISA
Reactivity: Human
Applications: AC
Applications: AC
Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: IHC, WB, ELISA, IP
Reactivity: Human
Applications: ELISA
Reactivity: Human

Recombinant Monoclonal Antibody

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