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Defects in SGCD are the cause of cardiomyopathy dilated type 1L (CMD1L) [MIM:606685]
Mutations in this gene have been associated with thrombophilia due to protein C deficiency
Catalogue Numbers: DF12369-100
Extra Notes: Western blot analysis of Claudin 5 on human lung cells lysates using anti-Claudin 5 antibody at 1/500 dilution
Specificity: Pan Lactic acid-Lysine polyclonal antibody detects endogenous levels of Pan Lactic acid-Lysine protein
CPEB3 Polyclonal Antibody-BS72589 primary and hard-to-transfect cells Defects in SGCD are theCPEB3 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,