Anticorpi Phospholipase C gamma 1 + 2

6 prodotti

Phospholipase C gamma 1 + 2 è un gene codificato dal simbolo PLCG2. Comunemente indicato anche come: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2; Phosphoinositide phospholipase C-gamma-2; Phospholipase C-IV; PLC-IV; Phospholipase C-gamma-2; PLC-gamma-2; PLCG2. Phospholipase C gamma 1 + 2 ha una massa di 147.87kDa, una lunghezza di amminoacidi di 1265, ed è implicato nella malattia: Familial cold autoinflammatory syndrome 3; Autoinflammation, antibody deficiency, and immune dysregulation PLCG2-associated.

Offriamo 6 anticorpi contro Phospholipase C gamma 1 + 2, allevati nel Coniglio, che sono adatti per WB, IHC, ELISA e ICC/IF con campioni derivati ​​da Umano, Topo e Ratto.

Informazioni su geni e proteine

Riepilogo UniProt
The production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) is mediated by activated phosphatidylinositol-specific phospholipase C enzymes. It is a crucial enzyme in transmembrane signaling.
Sommario di Entrez
The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of receptor-mediated tyrosine kinase activators. For example, when activated by SRC, the encoded protein causes the Ras guanine nucleotide exchange factor RasGRP1 to translocate to the Golgi, where it activates Ras. Also, this protein has been shown to be a major substrate for heparin-binding growth factor 1 (acidic fibroblast growth factor)-activated tyrosine kinase. Two transcript variants encoding different isoforms have been found for this gene.
Coinvolgimento nella malattia
Familial cold autoinflammatory syndrome 3: An autosomal dominant immune disorder characterized by the development of cutaneous urticaria, erythema, and pruritis in response to cold exposure. Affected individuals have variable additional immunologic defects, including antibody deficiency, decreased numbers of B-cells, defective B-cells, increased susceptibility to infection, and increased risk of autoimmune disorders.

Autoinflammation, antibody deficiency, and immune dysregulation PLCG2-associated: An autosomal dominant systemic disorder characterized by recurrent blistering skin lesions with a dense inflammatory infiltrate and variable involvement of other tissues, including joints, the eye, and the gastrointestinal tract. Affected individuals have a mild humoral immune deficiency associated with recurrent sinopulmonary infections, but no evidence of circulating autoantibodies.
Modifica post-translazionale
Phosphorylated on tyrosine residues by CSF1R (By similarity). Phosphorylated on tyrosine residues by BTK and SYK; upon ligand-induced activation of a variety of growth factor receptors and immune system receptors. Phosphorylation leads to increased phospholipase activity.
Collegamenti al database
Immunohistochemistry - Anti-PLCG1 Antibody (B0080) - Antibodies.com
(2)
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Western Blot - Anti-PLCG1 (phospho Tyr771) Antibody (A0079) - Antibodies.com
(5)
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Immunohistochemistry - Anti-PLCG1 Antibody (B0079) - Antibodies.com
(2)
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Segnaposto immagine Antibodies.com - Scopri di più spendendo meno
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Western Blot - Anti-PLCG1 (phospho Tyr1253) Antibody (A0551) - Antibodies.com
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Immunofluorescence - Anti-PLCG1 Antibody (B0551) - Antibodies.com
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