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Defects in the MESP2 gene are the cause of an autosomal recessive disorder known as spondylocostal dysostosis type 2 (SCDO2)
Background: KCNA3 mediates the voltage-dependent potassium ion permeability of excitable membranes
Veli-associated MAGUK 1
Rab 20 plays an important role in apical endocytosis and recycling and may be involved in the development of exocrine pancreatic adenocarcinomas
Alternative Names: Metalloproteinase inhibitor 2
PTH/PTHrP-R (L187) Polyclonal Antibody-BS2710 Size:100µl Defects in the MESP2 genePTH PTHrP R (L187) Polyclonal Antibody Product: Rabbit IgG, 1mg ml in PBS with 0. 02% sodium azide, 50% glycerol, pH7. 2 Catalogue Numbers: BS2710 50, BS2710 100 Sizes: 50l, 100l Swiss Prot: Q03431 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, IHC, IF Background: Parathyroid hormone (PTH), which is also designated parathyrin, is an 84 amino acid single chain peptide that functions to regulate calcium metabolism by raising blood levels
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