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Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene.
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37 results for "WHIP" in Products

37 results for "WHIP" in Products

WHIP Products

Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging. The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain. This protein shows homology to replication factor C family proteins, and is conserved from E. coli to human. Studies in yeast suggest that this gene may influence the aging process. Two transcript variants encoding different isoforms have been isolated for this gene.
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Applications: WB
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB
Reactivity: Human
Applications: IHC, WB, ELISA
Reactivity: Human
Applications: WB
Reactivity: Human
Applications: AC
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, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, IP
Reactivity: Human
Applications: IHC, 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, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
Applications: IHC, WB, IP
Reactivity: Human
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