Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
HPS3 encodes a protein containing a potential clathrin-binding motif, consensus dileucine signals, and tyrosine-based sorting signals for targeting to vesicles of lysosomal lineage. Zusätzlich bieten wir Ihnen Hermansky-Pudlak Syndrome 3 Kits (12) und Hermansky-Pudlak Syndrome 3 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 49 products:
Human Polyclonal HPS3 Primary Antibody für ELISA, WB - ABIN250258
Gautam, Chintala, Li, Zhang, Tan, Novak, Di Pietro, DellAngelica, Swank: The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2). in The Journal of biological chemistry 2004
HPS3 mutation is associated with high hypopigmentation in Hermansky-Pudlak syndrome.
Description of mutations in HPS (zeige HPS1 Antikörper) genes that cause Hermansky-Pudlak syndrome (review)
HPS4 but not HPS3 associates with HPS1 in a complex, which we term biogenesis of lysosome-related organelles complex 3 (BLOC-3)
Component of BLOC-2 (zeige HPS6 Antikörper). Results suggest a common biological basis underlying the pathogenesis of HPS-3, -5 and -6 disease.
A specific subset of melanocyte proteins are aberrantly trafficked throughout the HPS-3 melanocyte and may be responsible for the reduction in melanin synthesis.
HPS3 associates with clathrin, predominantly on small clathrin-containing vesicles in the perinuclear region. This association most likely occurs directly via a functional clathrin-binding domain in HPS3.
mutational analysis in Ashkenazi Jews with Hermansky-Pudlak syndrome 3
HPS3 is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2 (zeige HPS6 Antikörper))
This gene encodes a protein containing a potential clathrin-binding motif, consensus dileucine signals, and tyrosine-based sorting signals for targeting to vesicles of lysosomal lineage. The encoded protein may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 3. Alternate splice variants exist, but their full length sequence has not been determined.
Hermansky-Pudlak syndrome 3 protein
, Hermansky-Pudlak syndrome 3
, Hermansky-Pudlak syndrome 3 homolog
, Hermansky-Pudlak syndrome 3 protein homolog
, cocoa protein