Recombinant Human PCSK9 protein (Myc Tag, His Tag)
Cat no : Eg0199
Validation Data Gallery
Product Information
Purity | >95 %, SDS-PAGE |
Endotoxin | <0.1 EU/μg protein, LAL method |
Activity |
Immobilized Human PCSK9 (Myc tag, His tag) at 2 μg/mL (100 μL/well) can bind Biotinylated Human LDL R (GST tag) with a linear range of 3-12 ng/mL. |
Expression | HEK293-derived Human PCSK9 protein Gln31-Gln692 (Accession# Q8NBP7) with a Myc tag and a His tag at the C-terminus. |
GeneID | 255738 |
Accession | Q8NBP7 |
PredictedSize | 13.8 kDa (Propeptide) and 62.3 kDa (mature chain) |
SDS-PAGE | 17 kDa (Propeptide) and 65-75 kDa (mature chain), reducing (R) conditions |
Formulation | Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization. |
Reconstitution | Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water. |
Storage Conditions |
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping | The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature. |
Background
Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a crucial protein governing the circulating levels of low density lipoprotein-cholesterol (LDL-C), by virtue of its pivotal role in the degradation of the LDL receptor (LDLR). PCSK9 is expressed in the kidney and lung. It is synthesized as a 72 kDa immature precursor that undergoes autocatalytic cleavage in the endoplasmic reticulum to generate a 63 kDa mature protein. The cleaved N-terminal fragment remains associated with the mature protein and is necessary for its secretion, allowing it to circulate in the blood. The ability of PCSK9 to regulate a diverse group of cell-surface proteins hinted that it might also be able to influence additional membrane proteins that are important in anti-tumour immune responses. Targeting PCSK9 to treat cancer is also attractive because two neutralizing antibodies against it, evolocumab and alirocumab, have already been approved for human clinical use to lower cholesterol levels.
References:
1. Blanchard V, et al. (2019) Pathology. Feb;51(2):177-183. 2. Sharotri V, et al. (2012) J Biol Chem. Jun 1;287(23):19266-74 3. Canuel M, et al. (2013) PLoS One. May 13;8(5):e64145.
Publications
Species | Title |
---|---|
Mol Ther Engineered extracellular vesicles as nanosponges for lysosomal degradation of PCSK9 |