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HPS1 Rabbit anti-Human, Polyclonal, Proteintech
SDP

Rabbit Polyclonal Antibody

Supplier:  Proteintech Group Inc 150771AP150UL

Encompass_Preferred

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Catalog No. 50-172-9957


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Description

Description

Hermansky-Pudlak syndrome (HPS) is a rare, genetically heterogeneous, autosomal recessive disorder. It is characterized by oculocutaneous albinism, lysosomal storage defects and prolonged bleeding due to platelet storage pool deficiency. There are 10 HPS genes encoding HPS proteins that all interact within three distinct ubiquitously expressed protein complexes or biogenesis of lysosome-related organelle complexes. Defects in these genes cause HPS. HSP-1 is a component of multiple cytoplasmic organelles and is important for their normal development and function. It plays a role in intracellular protein sorting.
Specifications

Specifications

HPS1
Polyclonal
Unconjugated
HPS1
Hermansky Pudlak syndrome 1, HPS, HPS1
Rabbit
Antigen Affinity Chromatography
RUO
3257
-20°C
Liquid
Immunocytochemistry, Immunofluorescence, Western Blot
0.24 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
Q92902
HPS1
HPS1 Fusion Protein Ag7149
150 μL
Primary
Human
Antibody
IgG
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