RET Extracellular Domain (human, recombinant)

RET Extracellular Domain (human, recombinant)

CAT N°: 33987
Price:

602.00 511.70

Rearranged during transfection (RET) is a receptor tyrosine kinase with roles in cell proliferation, survival, metabolism, and migration, as well as in the development of the peripheral and central nervous systems.{60954,60955} It is composed of an extracellular domain, containing four cadherin-like domains (CLDs), a calcium-binding site, and a cysteine-rich region, a transmembrane domain, and an intracellular kinase domain.{60954,60956} RET forms heterodimeric complexes with the glial cell line-derived neurotrophic factor (GDNF) ligands GDNF, neurturin (NRTN), artemin (ARTN), and persephin (PSPN), and the GDNF family co-receptors GFR?1-4, which induces autophosphorylation of the intracellular kinase domain and activates cellular signaling.{60956} Germline nonsense and/or missense mutations in RET decrease functional RET in gut tissue during development and are associated with Hirschsprung’s disease.{60954,60956} Loss-of-function mutations in RET are associated with congenital anomalies of the kidney and urinary tract (CAKUT) and renal agenesis.{60956} Gain-of-function mutations in RET are associated with medullary thyroid cancer, pheochromocytoma, and parathyroid hypoplasias, and RET gene fusions have been found in patients with lung, colon, or breast carcinomas.{60955,60956} Cayman’s RET Extracellular Domain (human, recombinant) protein can be used for enzyme activity assays.

Territorial Availability: Available through Bertin Technologies only in France

  • Correlated keywords
    • CDHF-12 CDHR-16 RET-51 PTC GFR?2 GFR?3 GFR?4 GFR?-1 2 3 4
  • Product Overview:
    Rearranged during transfection (RET) is a receptor tyrosine kinase with roles in cell proliferation, survival, metabolism, and migration, as well as in the development of the peripheral and central nervous systems.{60954,60955} It is composed of an extracellular domain, containing four cadherin-like domains (CLDs), a calcium-binding site, and a cysteine-rich region, a transmembrane domain, and an intracellular kinase domain.{60954,60956} RET forms heterodimeric complexes with the glial cell line-derived neurotrophic factor (GDNF) ligands GDNF, neurturin (NRTN), artemin (ARTN), and persephin (PSPN), and the GDNF family co-receptors GFR?1-4, which induces autophosphorylation of the intracellular kinase domain and activates cellular signaling.{60956} Germline nonsense and/or missense mutations in RET decrease functional RET in gut tissue during development and are associated with Hirschsprung’s disease.{60954,60956} Loss-of-function mutations in RET are associated with congenital anomalies of the kidney and urinary tract (CAKUT) and renal agenesis.{60956} Gain-of-function mutations in RET are associated with medullary thyroid cancer, pheochromocytoma, and parathyroid hypoplasias, and RET gene fusions have been found in patients with lung, colon, or breast carcinomas.{60955,60956} Cayman’s RET Extracellular Domain (human, recombinant) protein can be used for enzyme activity assays.

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