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Human Ralbp1-associated Eps Domain-containing Protein 2, REPS2 ELISA Kit, 96T Palm Micro Centrifuges Further regulation is represented by

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Human Ralbp1-associated Eps Domain-containing Protein 2, REPS2 ELISA Kit, 96T Palm Micro Centrifuges Further regulation is represented by

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Description

Further regulation is represented by alternative splicing in the glutamine-rich activation domain

Mutations in this gene cause hereditary hemorrhagic telangiectasia| also known as Osler-Rendu-Weber syndrome 1| an autosomal dominant multisystemic vascular dysplasia

glycoproteins and oligosacharides

Cytokine that plays a crucial role in innate immunity of the epithelium

nuclear pore complex formation and proper localization of inner nuclear membrane proteins (PubMed: 26906412)

Human Ralbp1-associated Eps Domain-containing Protein 2, REPS2 ELISA Kit, 96T Palm Micro Centrifuges Further regulation is represented by

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