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PCSK9 AntibodyPeptide-affinity purified goat antibody

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AF1799a 0.1mg 400 ul 7-10 days $ 325.00 Add to cart
  • Specification
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PCSK9 Antibody - Product info

Other AccessionNP_777596
ReactivityHuman
Concentration100ug/200ul
IsotypeIgG

PCSK9 Antibody - Additional info

Other Names
PCSK9; FH3; NARC1; HCHOLA3; proprotein convertase subtilisin/kexin type 9; neural apoptosis regulated convertase 1; hypercholesterolemia, autosomal dominant 3; proprotein convertase subtilisin/kexin type 9; LDLCQ1; NARC-1
Format
0.5 mg IgG/ml in Tris saline (20mM Tris pH7.3, 150mM NaCl), 0.02% sodium azide, with 0.5% bovine serum albumin
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
PCSK9 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.

PCSK9 Antibody - Application data

  • AF1799a staining (0.2 µg/ml) of McA cell lysates: untransfected (1), transfected with wild type human pcsk9 (2), transfected with S127R human pcsk9 (3). Data kindly provided by Dr. X-M Sun, Hammersmith Hospital, London.

PCSK9 Antibody - Related products

AP7333a: PCSK9 Antibody (N-term)

AP7333b: PCSK9 Antibody (C-term)

RI13860: PCSK9 predesign siRNA

BP7333a: PCSK9 Antibody (N-term) Blocking Peptide

BP7333b: PCSK9 Antibody (C-term) Blocking Peptide

AF1799a: PCSK9 Antibody

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Provided below are standard protocols that you may find useful for product applications.

BACKGROUND

This gene encodes a proprotein convertase belonging to the proteinase K subfamily of the secretory subtilase family. The encoded protein is synthesized as a soluble zymogen that undergoes autocatalytic intramolecular processing in the endoplasmic reticulum. The protein may function as a proprotein convertase. This protein plays a role in cholesterol homeostasis and may have a role in the differentiation of cortical neurons. Mutations in this gene have been associated with a third form of autosomal dominant familial hypercholesterolemia (HCHOLA3).

REFERENCES

Pharmacogenetic analysis of lipid responses to rosuvastatin in Chinese patients. Hu M, et al. Pharmacogenet Genomics, 2010 Oct. PMID 20679960. An approach based on a genome-wide association study reveals candidate loci for narcolepsy. Shimada M, et al. Hum Genet, 2010 Oct. PMID 20677014. Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086. PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease: 3 independent studies and meta-analyses. Benn M, et al. J Am Coll Cardiol, 2010 Jun 22. PMID 20579540. Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population. Fontaine-Bisson B, et al. Diabetologia, 2010 Oct. PMID 20571754.