KO-Validated PCSK9 Recombinant Rabbit Monoclonal Antibody

KO-Validated PCSK9 Recombinant Rabbit Monoclonal Antibody

Cat: KVAb00091
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC

Reactivity:Human
Conjugate:Unconjugated
Gene Name:PCSK9
Category: KO&KD Validated Antibodies Tags: , , , , , , , , , , ,

Summary

Production Name

KO-Validated PCSK9 Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

PCSK9

Alternative Names

PCSK9; Proprotein Convertase Subtilisin/Kexin Type 9; NARC-1; FH3; Subtilisin/Kexin-Like Protease PC9; HCHOLA3; NARC1; PC9; Convertase Subtilisin/Kexin Type 9 Preproprotein; Hypercholesterolemia, Autosomal Dominant 3; Neural Apoptosis Regulated Convertase 1; Neural Apoptosis-Regulated Convertase 1; Proprotein Convertase 9; EC 3.4.21.111; EC 3.4.21.-; EC 3.4.21; LDLCQ1; FHCL3

Gene ID

255738

SwissProt ID

Q8NBP7

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000

Molecular Weight

Calculated MW: 74.3kDa

 

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]

 

Research Area

Signal Transduction,Cardiovascular,Stem Cells,Cell Biology,Metabolism,Neuroscience

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