NitroDIGE analysis reveals inhibition of protein S-nitrosylation by epigallocatechin gallates in lipopolysaccharide-stimulated microglial cells.

NitroDIGE analysis reveals inhibition of protein S-nitrosylation by epigallocatechin gallates in lipopolysaccharide-stimulated microglial cells.NitroDIGE analysis reveals inhibition of protein S-nitrosylation by epigallocatechin gallates in lipopolysaccharide-stimulated microglial cells. Related Articles

NitroDIGE analysis reveals inhibition of protein S-nitrosylation by epigallocatechin gallates in lipopolysaccharide-stimulated microglial cells.

J Neuroinflammation. 2014;11:17

Authors: Qu Z, Meng F, Zhou H, Li J, Wang Q, Wei F, Cheng J, Greenlief CM, Lubahn DB, Sun GY, Liu S, Gu Z

Abstract
BACKGROUND: Nitric oxide (NO)

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Developmental stage

This subsection of the ‘Expression’ section provides information on the expression of the gene product at various stages of a cell, tissue or organism development. By default, the information is derived from experiments at the mRNA level, unless specified ‘at the protein level’.

Examples: Q925Q8, P33124, Q96EP1

Note: The content of the

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Disruption phenotype

This subsection of the ‘Pathology and Biotech’ section describes the in vivo effects caused by ablation of the gene (or one or more transcripts) coding for the protein described in the entry. This includes gene knockout and knockdown, provided experiments have been performed in the context of a whole organism or a specific tissue, and not at the si

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Disulfide bond

This subsection of the ‘PTM / Processing’ section describes the positions of cysteine residues participating in disulfide bonds.

Disulfide bond formation generally occurs in the endoplasmic reticulum by oxidation. Therefore disulfide bonds are mostly found in extracellular, secreted and periplasmic proteins, although they can also be formed in

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DNA binding

This subsection of the ‘Function’ section specifies the position and type of each DNA-binding domain present within the protein.

We annotate experimentally defined DNA-binding domains and conserved DNA-binding domains defined by the InterPro resources PROSITE, Pfam and SMART; examples include the AP2/ERF domain, the ETS domain, the Fork-Head

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