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GNA13 Polyclonal Antibody, 100ul Reservoirs disease:Defects in F8 are the

SKU: 39414664281

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GNA13 Polyclonal Antibody, 100ul Reservoirs disease:Defects in F8 are theGuanine nucleotide binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems.,PTM: Palmitoylation is critical for proper membrane localization and signaling.,PTM: Phosphorylation on Thr 203 by PKA destabilizes the heterotrimer of alpha, beta and gamma, and inhibits Rho activation.,Belongs to the G alpha family. G(12) subfamily.,subcellular location: Identified by mass spectrometry in melanosome

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Description

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

The most abundant form of NF-kappa-B is NFKB1 complexed with the product of the gene

This protein may select cystic fibrosis transmembrane conductance regulator protein (CFTR) for degradation as well as unfolded proteins in Alzheimer's disease

This intronless gene is thought to have been generated by retrotransposition of a fully processed PCBP-2 mRNA

and neutrophils

GNA13 Polyclonal Antibody, 100ul Reservoirs disease:Defects in F8 are theGuanine nucleotide binding proteins (G proteins) are involved as modulators or transducers in various transmembrane signaling systems.,PTM: Palmitoylation is critical for proper membrane localization and signaling.,PTM: Phosphorylation on Thr 203 by PKA destabilizes the heterotrimer of alpha, beta and gamma, and inhibits Rho activation.,Belongs to the G alpha family. G(12) subfamily.,subcellular location: Identified by mass spectrometry in melanosome

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