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EP4 Polyclonal Antibody, 100ul Cytokines disease:Defects in F8 are the

SKU: 18358836491

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EP4 Polyclonal Antibody, 100ul Cytokines disease:Defects in F8 are theProstaglandin E receptor 4 encoded by PTGER4 is a member of the G protein coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). This receptor can activate T cell factor signaling. It has been shown to mediate PGE2 induced expression of early growth response 1 (EGR1), regulate the level and stability of cyclooxygenase 2 mRNA, and lead to the phosphorylation of glycogen synthase kinase 3. Knockout studies

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Description

disease:Defects in F8 are the cause of hemophilia A (HEMA)

The hepatotrophic factor designated augmenter of liver regeneration (ALR) is thought to be one of the factors responsible for the extraordinary regenerative capacity of mammalian liver

A similar gene disrupted in mice is shown to be essential during trophoblast development and gastrulation

1 μm pore size and a 75 mm diameter PES membrane

MHC class II gene expression is controlled primarily at the transcriptional level by transcription factors that bind to the X and Y boxes| two highly conserved elements in the proximal promoter of MHC class II genes

EP4 Polyclonal Antibody, 100ul Cytokines disease:Defects in F8 are theProstaglandin E receptor 4 encoded by PTGER4 is a member of the G protein coupled receptor family. This protein is one of four receptors identified for prostaglandin E2 (PGE2). This receptor can activate T cell factor signaling. It has been shown to mediate PGE2 induced expression of early growth response 1 (EGR1), regulate the level and stability of cyclooxygenase 2 mRNA, and lead to the phosphorylation of glycogen synthase kinase 3. Knockout studies

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