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RAI1 Products

Defects in Retinoic acid-induced protein 1 (RAI1) are a cause of Smith-Magenis syndrome (SMS) [MIM:182290]. SMS is characterized by congenital mental retardation associated with development and growth delays. The RAI1 has also been associated with schizophrenia.
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31 results for "RAI1" in Products

31 results for "RAI1" in Products

RAI1 Products

Defects in Retinoic acid-induced protein 1 (RAI1) are a cause of Smith-Magenis syndrome (SMS) [MIM:182290]. SMS is characterized by congenital mental retardation associated with development and growth delays. The RAI1 has also been associated with schizophrenia.
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Applications: IHC, WB, IP
Reactivity: Human
Applications: WB, ELISA
Reactivity: Human
Applications: IHC, ICC/IF
Reactivity: Human
Applications: WB, ELISA, MA, AP
Applications: AC
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
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