SFTPC Primary Antibody

Item Information
Catalog #Size/ConcentrationPrice
Specification
AliasesSP-C; PSP-C; SFTP2; SMDP2
ProductOrderS
Clone#5E6A9
Entrez GenelD6440
FormulationPurified antibody in PBS with 0.05% sodium azide
HostMouse
IsotypeIgG1
ImmunogenPurified recombinant fragment of human SFTPC (AA: 60-180 ) expressed in E. Coli.
MW21kDa
Shipping InformationThis product will ship in a box containing blue ice at a temperature of 4°C. Learn More
Species ReactivityHuman
Application
ELISA1/10000
WB (Western Blot)1/500 - 1/2000
Sequence
60-180
Catalog#: 30441
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Images
Western Blot
Figure 1: Western blot analysis using SFTPC mAb against human SFTPC recombinant protein. (Expected MW is 38.4 kDa)
Figure 1: Western blot analysis using SFTPC mAb against human SFTPC recombinant protein. (Expected MW is 38.4 kDa)
Western Blot
Figure 2: Western blot analysis using SFTPC mAb against HEK293 (1) and SFTPC (AA: 60-180)-hIgGFc transfected HEK293 (2) cell lysate.
Figure 2: Western blot analysis using SFTPC mAb against HEK293 (1) and SFTPC (AA: 60-180)-hIgGFc transfected HEK293 (2) cell lysate.
Elisa
Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng);
Black line: Control Antigen (100 ng); Purple line: Antigen(10ng); Blue line: Antigen (50 ng); Red line: Antigen (100 ng);
Product Overview
DescriptionThis 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.

References (references)
References (references)1.Am J Respir Cell Mol Biol. 2011 Sep;45(3):498-509.
2.J Biol Chem. 2009 Nov 27;284(48):33377-83.
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