The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Blocking - Blocking peptide for Anti-HPS3 antibody (ab19047)
Concentration information loading...
Shipped at 4°C. Store at -20°C. Stable for 12 months at -20°C.
Hermansky Pudlak syndrome 3
Hermansky Pudlak syndrome 3 protein
HPS3, biogenesis of lysosomal organelles complex 2 subunit 1
HPS3 is involved in early stages of melanosome biogenesis and maturation. Defects in HPS3 are the cause of the cocoa (coa) mutant, and of Hermansky-Pudlak syndrome type 3 (HPS3). HPS3 is an autosomal recessive disorder, characterized by oculocutaneous albinism, bleeding due to platelet storage pool deficiency, and lysosomal storage defects. This syndrome results from defects of diverse cytoplasmic organelles including melanosomes, platelet dense granules and lysosomes. Ceroid storage in the lungs is associated with pulmonary fibrosis, a common cause of premature death in individuals with HPS.
has not yet been referenced specifically in any publications.