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F5F8D is an autosomal recessive human bleeding disorder characterized by the reduction of both clotting proteins
PPPDE1/PNAS4 Antibody
Catalogue Numbers: MB65914-50
MAL associates with unpolymerized actin through its RPEL motifs
Catalogue Numbers: AF3940-100
MBNL1 Polyclonal Antibody-BS71062 PolyMag F5F8D is an autosomal recessiveMBNL1 Polyclonal Antibody Sizes: 50l, 100l Catalogue Numbers: BS71062 50, BS71062 100 Product: 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Swiss Prot: Q9NR56 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC, IF ICC All Applications: WB,1: 500 1: 2000 IHC,1: 50 1: 100 IF ICC,1: 50 1: 100 Background: This gene encodes a member of the muscleblind protein family which was initially described in Drosophila melanogaster. The
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