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BBS2 Products

BBS2 encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. [provided by RefSeq]
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44 results for "BBS2" in Products

44 results for "BBS2" in Products

BBS2 Products

BBS2 encodes a protein of unknown function. Mutations in this gene have been observed in patients with Bardet-Biedl syndrome type 2. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation. [provided by RefSeq]
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Applications: WB
Reactivity: Human
Applications: WB, ELISA, MA, AP
Applications: WB
Reactivity: Human
Applications: ICC/IF
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: ICC/IF
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: IHC
Reactivity: Human
Applications: WB
Applications: WB, ELISA
Reactivity: Mouse, Rat
Catalog #: NBP3-42932
Applications: WB, ELISA, ICC/IF
Reactivity: Human, Canine
Applications: AC
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: WB
Reactivity: Human
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