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AACT deficiency may also be a possible cause of chronic liver disease
Mutations in this gene cause Chondrodysplasia punctata 2 (CDPX2
Catalogue Number: DF14505
Application: FC
the encoded protein contains an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain
Neuralized-1 (V250) Polyclonal Antibody-BS3342 Size:100µl AACT deficiency may also beNeuralized 1 (V250) Polyclonal Antibody Product: Rabbit IgG, 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Catalogue Numbers: BS3342 50, BS3342 100 Sizes: 50l, 100l Swiss Prot: O76050 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: IHC Background: NEURL is involved in the determination of cell fate in the neurogenic region of the embryo and plays a role in the determination of cell fate in the central nervous system. NEURL may
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