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PCSK9 (5G4) Mouse mAb

-YM33124

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Catalog: YM33124
Size
Price
Status
Qty.
200μL
$450.00
3 weeks

0

100μL
$280.00
3 weeks

0

40μL
$160.00
3 weeks

0

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Main Information
Target

PCSK9

Host Species

Mouse

Reactivity

Human

Applications

IHC

MW

74kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC1:50-200
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
This antibody detects endogenous levels of PCSK9 at Human, Mouse,Rat
Purification
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
74kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
5G4
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human PCSK9
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Specificity:
This antibody detects endogenous levels of PCSK9 at Human, Mouse,Rat
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Gene Name:
PCSK9 NARC1 PSEC0052
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Protein Name:
PCSK9
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Other Name:
Proprotein convertase subtilisin/kexin type 9 ;
Neural apoptosis-regulated convertase 1 ;
NARC-1 ;
Proprotein convertase 9 ;
PC9 ;
Subtilisin/kexin-like protease PC9 ;
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Database Link:
Organism Gene ID SwissProt
Human 255738; Q8NBP7;
Mouse 100102; Q80W65;
Rat 298296; P59996;
Background:
This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an autocatalytic processing event with its prosegment in the ER and is constitutively secreted as an inactive protease into the extracellular matrix and trans-Golgi network. It is expressed in liver, intestine and kidney tissues and escorts specific receptors for lysosomal degradation. It plays a role in cholesterol and fatty acid metabolism. Mutations in this gene have been associated with autosomal dominant familial hypercholesterolemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014],
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Function:
cofactor:Calcium.,Disease:Defects in PCSK9 are the cause of familial hypercholesterolemia 3 (FH3) [MIM:603776]. FH3 inheritance is autosomal dominant.,enzyme regulation:Inhibited by EGTA.,Function:May be implicated in the differentiation of cortical neurons and may play a role in cholesterol homeostasis.,PTM:The soluble zymogen undergoes autocatalytic intramolecular processing in the endoplasmic reticulum, resulting in the cleavage of its propeptide that remains associated with the secreted enzyme.,similarity:Belongs to the peptidase S8 family.,similarity:Contains 1 peptidase S8 domain.,subunit:The precursor protein but not the mature protein may form multimers.,tissue specificity:Expressed in neuro-epithelioma, colon carcinoma, hepatic and pancreatic cell lines, and in Schwann cells.,
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Cellular Localization:
Cytoplasm. Secreted. Endosome. Lysosome. Cell surface. Endoplasmic reticulum. Golgi apparatus. Autocatalytic cleavage is required to transport it from the endoplasmic reticulum to the Golgi apparatus and for the secretion of the mature protein. Localizes to the endoplasmic reticulum in the absence of LDLR and colocalizes to the cell surface and to the endosomes/lysosomes in the presence of LDLR. The sorting to the cell surface and endosomes is required in order to fully promote LDLR degradation.
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Tissue Expression:
Expressed in neuro-epithelioma, colon carcinoma, hepatic and pancreatic cell lines, and in Schwann cells.
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Research Areas:
>>Cholesterol metabolism
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Catalog: YM33124
Size
Price
Status
Qty.
200μL
$450.00
3 weeks

0

100μL
$280.00
3 weeks

0

40μL
$160.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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