SFTPC (NM_003018) Human Recombinant Protein

  • Product Brand Image
SKU
TP303246L
Recombinant protein of human surfactant protein C (SFTPC), 1 mg
  $7,820.00
6 Weeks*
Bulk/Customize
Specifications
Specifications
Product Data
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence
Protein Sequence
>RC203246 protein sequence
Red=Cloning site Green=Tags(s)

MDVGSKEVLMESPPDYSAAPRGRFGIPCCPVHLKRLLIVVVVVVLIVVVIVGALLMGLHMSQKHTEMVLE
MSIGAPEAQQRLALSEHLVTTATFSIGSTGLVVYDYQQLLIAYKPAPGTCCYIMKIAPESIPSLEALNRK
VHNFQMECSLQAKPAVPTSKLGQAEGRDAGSAPSGGDPAFLGMAVNTLCGEVPLYYI

TRTRPLEQKLISEEDLAANDILDYKDDDDKV
Tag C-Myc/DDK
Predicted MW 20.8 kDa
Concentration >0.05 µg/µL as determined by microplate BCA method
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3, 10% glycerol
Preparation Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
Note For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process.
Storage Store at -80°C.
Stability Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles.
Shipping Dry Ice
Reference Data
RefSeq NP_003009
Locus ID 6440
UniProt ID P11686
Cytogenetics 8p21.3
RefSeq Size 989
RefSeq ORF 591
Synonyms BRICD6; PSP-C; SFTP2; SMDP2; SP-C; SP5
Summary 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.provided by RefSeq, Feb 2010
Protein Categories Intracellular Proteins, Secreated Proteins
Protein Families Secreted Protein, Transmembrane
Reviews
 
 
 
 
 

Be the first to review this product

Please note:
Only reviews with images are eligible for a $20/20€ Amazon gift card.
Reviews without images are eligible for a $10/10€ Amazon gift card.
For more details about the terms and conditions, please visit the promotion page.

Review image
Documents
Resources

file-alt Citations

Pulmonary Surfactant Proteins are Inhibited by IgA Autoantibodies in Severe COVID-19
Sinnberg, Lichtensteiger, Hasan Ali et al
Am J Respir Crit Care Med (2022)
Cited by 1
AI Summary: OriGene’s recombinant pulmonary surfactant-associated protein B (Cat. No. TP324088) and protein C (Cat. No. TP303246) were used as antigens in ELISA assays to detect IgA autoantibodies in patient samples, helping demonstrate that these autoantibodies target and inhibit lung surfactant proteins in severe COVID-19.
Snippet: …TP324088 or Cat. … TP303246, respectively;or in-house expressed in HEK293 cells and affinity-purified) were coated in 100 µL of 0.05 M carbonate-bicarbonate buffer, pH 9.6 per well using 96-well flat-bottom MediSorp plates (Thermo Fisher Scientific) at 4 °C overnight. …
Showing 1-1 of 1 papers.
Powered by BizGenius
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Related Products