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Three isoforms of TMEM16A exist due to alternative splicing events
Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis
Background: The diastrophic dysplasia sulfate transporter is a transmembrane glycoprotein implicated in the pathogenesis of several human chondrodysplasias
angiogenesis andmitogenesis
Variations in ADH7 may be associated with alcohol dependence
Hepatitis A Virus Cellular Receptor 1 Monoclonal Antibody-MB11808 Affinity Biosciences Three isoforms of TMEM16A existHepatitis A Virus Cellular Receptor 1 Monoclonal Antibody Sizes: 50l, 100l Catalogue Numbers: MB11808 50, MB11808 100 Product: 50mM Tris Glycine(pH 7. 4), 0. 15M NaCl, 40% Glycerol, 0. 01% Sodium azide and 0. 05% BSA Swiss Prot: Q96D42 Host: Rabbit Reactivity: Human, Mouse, Rat Applications: WB, All Applications: WB: 1 500 1 1000 Background: May play a role in T helper cell development and the regulation of asthma and allergic diseases. Receptor for
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