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Mutations in this gene have been associated with thrombophilia due to protein C deficiency
Catalogue Numbers: BS5731-50
Defects in SGCD are the cause of cardiomyopathy dilated type 1L (CMD1L) [MIM:606685]
Immunogen: Recombinant fusion protein of human CPS1(NP_001116105
Expressed primarily in the fetal brain
CPEB3 Polyclonal Antibody-BS72589 primary and hard-to-transfect cells Mutations in this gene haveCPEB3 Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS72589 50, BS72589 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q8NE35 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC, IF ICC All Applications: WB,1: 200 1: 2000 IHC,1: 50 1: 200 IF ICC,1: 50 1: 200 Background: Sequence specific RNA binding protein which acts as a translational repressor in the basal unstimulated state but,
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