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SFTPC encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Additionally we are shipping Surfactant Protein C Kits (53) and Surfactant Protein C Proteins (9) and many more products for this protein.
Showing 10 out of 121 products:
Human Polyclonal Surfactant Protein C Primary Antibody for FACS, IF (p) - ABIN1387397
Yan, Xiaoli, Guoliang, Zhonghui, Di, Ximeng, Piye, Li, Lin: SB203580 inhibits epithelial-mesenchymal transition and pulmonary fibrosis in a rat silicosis model. in Toxicology letters 2016
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Human Monoclonal Surfactant Protein C Primary Antibody for ELISA, WB - ABIN1098147
Zhong, Zhou, Ann, Minoo, Liu, Banfalvi, Krishnaveni, Dubourd, Demaio, Willis, Kim, duBois, Crandall, Beers, Borok: Role of endoplasmic reticulum stress in epithelial-mesenchymal transition of alveolar epithelial cells: effects of misfolded surfactant protein. in American journal of respiratory cell and molecular biology 2011
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Human Monoclonal Surfactant Protein C Primary Antibody for ELISA, WB - ABIN520151
Wong, Keating, Lu, Duchesneau, Wang, Sacher, Hu, Waddell: Identification of a bone marrow-derived epithelial-like population capable of repopulating injured mouse airway epithelium. in The Journal of clinical investigation 2009
Human Polyclonal Surfactant Protein C Primary Antibody for FACS - ABIN2179378
Vadasz, Jensen, Moncada, Girard, Zhang, Blanchette, Finck: Second and third trimester amniotic fluid mesenchymal stem cells can repopulate a de-cellularized lung scaffold and express lung markers. in Journal of pediatric surgery 2014
This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.
surfactant protein C
, surfactant, pulmonary-associated protein C
, pulmonary surfactant-associated protein C
, pulmonary surfactant-associated proteolipid SPL(Val)
, BRICHOS domain containing 6
, pulmonary surfactant apoprotein-2 SP-C
, Surfactant pulmonary-associated protein C
, Surfactant, pulmonary-associated protein C
, surfactant associated protein C
, type I SP-C
, type II SP-C