SKU: WP16995 Categories: ,

BL1S3 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP16995-100
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Product details

Background:

This gene encodes a protein that is a component of the BLOC1 multi-subunit protein complex. This complex is necessary for the biogenesis of specialized organelles of the endosomal-lysosomal system, including platelet dense granules and melanosomes. Mutations in this gene cause Hermansky-Pudlak syndrome 8, a disease characterized by lysosomal storage defects, bleeding due to platelet storage pool deficiency, and oculocutaneous albinism. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetBL1S3
ReactivityHuman, Mouse
ApplicationsWB
MW(Calculated)22kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human BL1S3 AA range: 142-192
SpecificityThis antibody detects endogenous levels of BL1S3 at Human/Mouse
Gene NameBLOC1S3 BLOS3
Protein NameBL1S3
Other Name
SpeciesHuman
Gene ID388552
UniprotQ6QNY0,
Species.1Mouse
Gene ID.1232946
Uniprot.1Q5U5M8
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationCytoplasm .
Tissue Expression
Signaling_pathway
Research Areas
FunctionDisease:Defects in BLOC1S3 are the cause of Hermansky-Pudlak syndrome type 8 (HPS8) [MIM:203300]. Hermansky-Pudlak syndrome (HPS) is a genetically heterogeneous, rare, 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.,Function:May play a role in the biogenesis of melanosomes and other specialized organelles of the endosomal-lysosomal system.,PTM:Phosphorylated.,similarity:Belongs to the BLOC1S3 family.,subunit:Component of the biogenesis of lysosome-related organelles (BLOC-1) complex which is composed of BLOC1S1, BLOC1S2, DTNBP1, MUTED, PLDN, CNO/cappuccino and SNAPAP. Interacts directly with BLOC1S2.,
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