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Recombinant Human HPS6 Protein, N-His-SUMO

Reference: ARO-P11428
Product nameRecombinant Human HPS6 Protein, N-His-SUMO
Origin speciesHuman
Expression systemProkaryotic expression
Molecular weight21.54 kDa
BufferLyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
FormLiquid
Delivery conditionDry Ice
Delivery lead time in business days3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term (1 week), -20°C or -80°C for long term (avoid freezing/thawing cycles; addition of 20-40% glycerol improves cryoprotection)
BrandAntibodySystem
Host speciesEscherichia coli (E.coli)
Fragment TypeThr371-Met454
Aliases /SynonymsRuby-eye protein homolog, HPS6, Ru, Hermansky-Pudlak syndrome 6 protein
ReferenceARO-P11428
NoteFor research use only.

Description of Recombinant Human HPS6 Protein, N-His-SUMO

Introduction

Recombinant Human HPS6 Protein, also known as HPS6, is a highly conserved protein that plays a crucial role in the biogenesis of lysosome-related organelles. It is a member of the Hermansky-Pudlak Syndrome (HPS) protein family and is encoded by the HPS6 gene. HPS6 is involved in the formation of intracellular organelles such as melanosomes, platelet dense granules, and lysosomes. In this article, we will discuss the structure, activity, and application of Recombinant Human HPS6 Protein.

Structure of Recombinant Human HPS6 Protein

Recombinant Human HPS6 Protein is a 115-kDa protein consisting of 1,015 amino acids. It is composed of multiple domains, including a coiled-coil domain, a WD40 repeat domain, and a C-terminal domain. The coiled-coil domain is responsible for protein-protein interactions, while the WD40 repeat domain is involved in protein-protein interactions and protein-DNA interactions. The C-terminal domain contains a conserved motif that is essential for the localization of HPS6 to lysosome-related organelles.

Activity of Recombinant Human HPS6 Protein

HPS6 is primarily involved in the biogenesis of lysosome-related organelles. It is required for the proper trafficking of proteins to these organelles and plays a crucial role in the formation of their characteristic morphology. HPS6 interacts with other HPS proteins, such as HPS1, HPS4, and HPS5, to form a complex that is essential for the proper function of lysosome-related organelles.

Studies have shown that mutations in the HPS6 gene can lead to Hermansky-Pudlak Syndrome, a rare genetic disorder characterized by abnormal pigmentation, bleeding disorders, and lung fibrosis. This further highlights the importance of HPS6 in the biogenesis of lysosome-related organelles and its role in maintaining cellular homeostasis.

Application of Recombinant Human HPS6 Protein

Recombinant Human HPS6 Protein has various applications in the field of cell biology and medicine. It can be used in research studies to understand the mechanisms involved in the biogenesis of lysosome-related organelles. Recombinant HPS6 protein can also be used to study the pathophysiology of Hermansky-Pudlak Syndrome and other related disorders.

Furthermore, Recombinant Human HPS6 Protein has potential therapeutic applications. Mutations in the HPS6 gene have been linked to various disorders, and the use of recombinant HPS6 protein may help in the development of targeted therapies for these conditions. Additionally, HPS6 has been shown to interact with other proteins involved in lysosome-related organelle biogenesis, making it a potential target for drug development.

Conclusion

In summary, Recombinant Human HPS6 Protein is a crucial protein involved in the biogenesis of lysosome-related organelles. It plays a vital role in maintaining cellular homeostasis and is essential for the proper function of these organelles. Recombinant HPS6 protein has various applications in research and medicine, and its study may lead to a better understanding of related disorders and the development of targeted therapies.

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