IKK gamma Polyclonal Antibody, 100ul[BT-AP10268] Thermal Control Mutations in this gene are

Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy

This gene encodes the A-chain polypeptide of human complement subcomponent C1q

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The gene is located near the Smith-Magenis syndrome region on chromosome 17

IKK gamma Polyclonal Antibody, 100ul[BT-AP10268] Thermal Control Mutations in this gene areThis gene encodes the regulatory subunit of the inhibitor of kappaB kinase (IKK) complex, which activates NF kappaB resulting in activation of genes involved in inflammation, immunity, cell survival, and other pathways. Mutations in this gene result in incontinentia pigmenti, hypohidrotic ectodermal dysplasia, and several other types of immunodeficiencies. A pseudogene highly similar to this locus is located in an adjacent region of the X chromosome.