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Western blot - PCSK9 antibody - Propeptide domain (ab42085)
Western blot - PCSK9 antibody - Propeptide domain (ab42085)
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Product Name 

PCSK9 antibody - Propeptide domain

 

See all PCSK9 antibodies (6)...

Product type 

Primary antibodies

Description 

Rabbit polyclonal to PCSK9 - Propeptide domain

Immunogen 

Synthetic peptide corresponding to the propeptide domain of Human PCSK9.
(the amino acid sequence is considered proprietary)(Peptide available as ab44562.)

Reacts with 
(species key)

Hu

Specificity 

ab42085 recognises PCSK9 in teh region corresponding to the propeptide cleave site, and detects both the zymogen and active PCSK9.

We have a range of domain specific antibodies for this target. For a full list please see all PCSK9 antibodies

Tested applications 
(see key)

WB


Abreviews 

Customer reviews
(see key)


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Application notes 
(see key)

Recommended dilutions
WB: 1/1000 - 1/5000. Predicted molecular weights: ~15 and 74 kDa. Recommended starting dilution 1/1000 with colourimetric substrates, 1:5000 with chemiluminescent substrates. Dilution optimised using Chromogenic detection. Not yet tested in other applications. Optimal dilutions/concentrations should be determined by the end user.



Specific protocols
Recommended WB protocol

Cellular localization 

Secreted

Research areas 

Cell Biology >> Proteolysis / Ubiquitin >> Proteolytic enzymes >> Serine protease >> Proprotein Convertases
Signal Transduction >> Metabolism >> Lipid metabolism
Stem Cells >> Neural Stem Cells >> Intracellular
Cardiovascular >> Lipids / Lipoproteins >> Lipid Metabolism >> Cholesterol Metabolism
Signal Transduction >> Metabolism >> Amino Acids

Relevance 

PCSK9 is a proprotein convertase belonging to the proteinase K subfamily of the secretory subtilase family. PCSK9 is synthesized as a soluble zymogen that undergoes autocatalytic intramolecular processing in the endoplasmic reticulum. PCSK9 may function as a proprotein convertase. PCSK9 plays a role in cholesterol homeostasis and may have a role in the differentiation of cortical neurons. Mutations in PCSK9 gene have been associated with a third form of autosomal dominant familial hypercholesterolemia.

 

Alternative names for PCSK9 antibody - Propeptide domain (ab42085)

Database links 

The links below go to external sites and will open in a new browser window

Entrez Gene

    

255738  (Human)

GeneCard

    

GC01P055277  (Human)