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Each lot of this antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 10 µl per 5 ml antibody dilution buffer for each mini-gel. It is recommended that the reagent be titrated for optimal performance for each application.
HepG2 cell extract was resolved by electrophoresis, transferred to nitrocellulose, and probed with rabbit anti-α-adducin antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.
The α-adducin protein is a ubiquitously expressed cytoskeletal protein that binds with high affinity to Ca2+/calmodulin and acts as a substrate for protein kinases A and C. α-addducin is a 80-120 kD member of the aldolase class II family and adducin subfamily. This protein has three isoforms that interact as heterodimers α/β, and α/γ. The molecular weights for the various isoforms are α=120 kD; β=110kD; γ=80kD. This protein has been reported to promote the assembly of the spectrin-actin network. Polymorphisms in α-adducin are associated with cardiovascular disease and hypertension. α-adducin has been reported to interact with calmodulin. When phosphorylated by Rho-kinase, α-adducin can regulate membrane ruffling and cell motility. The Poly6170 antibody has been shown to be useful for Western blotting of mouse and human α-adducin protein.
Other Names:
ADD-1
Structure:
Aldolase class II family, adducin subfamily, heterodimerizes α/β, α/γ. Multiple isoforms α-120 kD, β-110 kD, γ-80kD
Distribution:
Ubiquitously expressed cytoskeletal protein
Function:
Binds with high affinity to Ca2+/calmodulin, substrate for protein kinases A and C, promotes the assembly of spectrin-actin network. Polymorphisms associated with cardiovascular disease and hypertension
Regulation:
Phosphorylation by Rho-kinase regulates membrane ruffling, cell motility
Modification:
Phosphorylation
Interaction:
Calmodulin
Antigen References:
1. Fukata Y, et al. 1999. J. Cell Biol. 145:347. 2. Joshi R, et al. 1991. J. Cell. Biol. 115:665. 3. Lin B, et al. 1995. Genomics 25:93.
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.
Purified anti-α-Adducin
HepG2 cell extract was resolved by electrophoresis, transferred to nitrocellulose, and probed with rabbit anti-α-adducin antibody. Proteins were visualized using a donkey anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.