Pay in 4 interest-free payments of $25.00 Learn more
Ships within 48 hours · Estimated delivery Aug 9 - Aug 14
Hereditary pulmonary alveolar proteinosis (hPAP) is a rare disorder of pulmonary surfactant accumulation and hypoxemic respiratory failure caused by mutations in GM-CSF receptor alpha
is a tumorigenic and high-glycosylated cell surface protein that has been proven to be linked with the carcinogenic effects in different solid tumors
Cytotoxic T-Lymphocyte-Associated Antigen 8
and take 500 uL of 1 × Binding Buffer to resuspend the cells
Clinical Biochemistry
NaPi2b/SLC34A2 Recombinant Rabbit mAb (SDT-R229) IHC Kits Hereditary pulmonary alveolar proteinosis (hPAP)Product Specification Host Rabbit Antigen NaPi2b SLC34A2 Synonyms Sodium dependent phosphate transport protein 2B, Sodium phosphate transport protein 2B, Na(+) dependent phosphate cotransporter 2B, NaPi3b, Sodium phosphate cotransporter 2B (Na(+) Pi cotransporter 2B; NaPi 2b), Solute carrier family 34 member 2 Location Apical cell membrane Accession O95436 Clone Number SDT R229 Antibody Type Recombinant mAb Isotype IgG Application WB, IHC P, ICC