PCSK9 Protein (AA 31-692) (His tag)
Aperçu rapide pour PCSK9 Protein (AA 31-692) (His tag) (ABIN2181580)
Antigène
Voir toutes PCSK9 ProtéinesType de proteíne
Activité biologique
Origine
Source
Pureté
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Attributs du protein
- AA 31-692
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Purification/Conjugué
- Cette PCSK9 protéine est marqué à la His tag.
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Séquence
- AA 31-692
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Attributs du produit
- This protein carries a polyhistidine tag at the C-terminus. The protein has a calculated MW of 75.1 kDa. The protein migrates as 20 kDa and 62 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation and proteolytic digestion.
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Stérilité
- 0.22 μm filtered
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niveau d'endotoxine
- Less than 1.0 EU per μg by the LAL method.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
- PBS, pH 7.4
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Conseil sur la manipulation
- Please avoid repeated freeze-thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- No activity loss was observed after storage at: In lyophilized state for 1 year (4 °C), After reconstitution under sterile conditions for 3 months (-70 °C).
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: "PCSK9 Activity Is Potentiated Through HDL Binding." dans: Circulation research, (2021) (PubMed).
: "Evolution of sequence-defined highly functionalized nucleic acid polymers." dans: Nature chemistry, Vol. 10, Issue 4, pp. 420-427, (2019) (PubMed).
: "Side chain determinants of biopolymer function during selection and replication." dans: Nature chemical biology, Vol. 15, Issue 4, pp. 419-426, (2019) (PubMed).
: "The hepatic WASH complex is required for efficient plasma LDL and HDL cholesterol clearance." dans: JCI insight, Vol. 4, Issue 11, (2019) (PubMed).
: "Low-density lipoprotein (LDL)-dependent uptake of Gram-positive lipoteichoic acid and Gram-negative lipopolysaccharide occurs through LDL receptor." dans: Scientific reports, Vol. 8, Issue 1, pp. 10496, (2018) (PubMed).
: "Retrograde cholesterol transport in the human Caco-2/TC7 cell line: a model to study trans-intestinal cholesterol excretion in atherogenic and diabetic dyslipidemia." dans: Acta diabetologica, Vol. 54, Issue 2, pp. 191-199, (2017) (PubMed).
: "The Proprotein Convertase Subtilisin/Kexin Type 9-resistant R410S Low Density Lipoprotein Receptor Mutation: A NOVEL MECHANISM CAUSING FAMILIAL HYPERCHOLESTEROLEMIA." dans: The Journal of biological chemistry, Vol. 292, Issue 5, pp. 1573-1590, (2017) (PubMed).
: "Lipopolysaccharide Is Cleared from the Circulation by Hepatocytes via the Low Density Lipoprotein Receptor." dans: PLoS ONE, Vol. 11, Issue 5, pp. e0155030, (2017) (PubMed).
: "Increased Plasma PCSK9 Levels Are Associated with Reduced Endotoxin Clearance and the Development of Acute Organ Failures during Sepsis." dans: Journal of innate immunity, Vol. 8, Issue 2, pp. 211-20, (2016) (PubMed).
: "PCSK9 is a critical regulator of the innate immune response and septic shock outcome." dans: Science translational medicine, Vol. 6, Issue 258, pp. 258ra143, (2015) (PubMed).
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- PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
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Autre désignation
- PCSK9
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Sujet
- Proprotein convertase subtilisin/kexin type 9 (PCSK9), is an enzyme which in humans is encoded by the PCSK9 gene. This gene encodes a proprotein convertase belonging to the proteinase K subfamily of the secretory subtilase family. This protein plays a major regulatory role in cholesterol homeostasis. PCSK9 binds to the epidermal growth factor-like repeat A (EGF-A) domain of the low-density lipoprotein receptor (LDLR), inducing LDLR degradation. PCSK9 may also have a role in the differentiation of cortical neurons. Mutations in this gene have been associated with a rare form of autosomal dominant familial hypercholesterolemia (HCHOLA3).
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Poids moléculaire
- 13.8 kDa and 58.1 kDa
Antigène
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