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Human CSF2 Ni-NTA Kits Mevalonate kinase deficiency caused by

SKU: 30305243794

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Description

Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria

IHC Host Rabbit Clone type rabbit monoclonal Target Background Predicted to enable store-operated calcium channel activity

This protein is the only one in the coagulation pathway for which a congenital deficiency has not been described

It is involved in a variety of other biological processes such as the regulation of the coagulation pathway

Human CSF2 Ni-NTA Kits Mevalonate kinase deficiency caused byBcakground Granulocyte Macrophage Growth Factor(GM CSF) is one of an array of cytokines with pivotal roles in embryo implantation and subsequent development. In response to cytokine or inflammatory stimuli, GM CSF is produced by a number of different cell types, including T cells, B cells, macrophages, mast cells, endothelial cells, fibroblasts, and adipocytes (1). As a survival factor, GM CSF activates the effector functions of granulocytes,

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