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Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2

TargetMol | SPR
Catalog No. TMPY-00873U

Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2 is expressed in HEK293 Cells. The accession number is P80188-1.

Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2

Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2

TargetMol | SPR
Catalog No. TMPY-00873U
Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2 is expressed in HEK293 Cells. The accession number is P80188-1.
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Product Information

Biological Activity
Immobilized Human NGAL, His Tag at 0.2 μg/ml (100 μl/Well) on the plate. Dose response curve for Anti-NGAL Antibody, hFc Tag with the EC50 of 7.8 ng/ml determined by ELISA.
Description
Lipocalin-2/LCN2 Protein, Human, Recombinant (His) V2 is expressed in HEK293 Cells. The accession number is P80188-1.
Species
Human
Expression System
HEK293 Cells
TagC-His
Accession NumberP80188-1
Synonyms
p25,NGAL,MSFI,Lipocalin-2,lipocalin 2,24p3
Construction
Gln21-Gly198
Protein Purity
> 95% as determined by Tris-Bis PAGE; > 95% as determined by HPLC
Molecular Weight21.64 kDa (Predicted); 25-30 kDa (Due to glycosylation)
Endotoxin< 1.0 EU/μg of the protein as determined by the LAL method.
FormulationLyophilized from 0.22 μm filtered solution in PBS (pH 7.4). Normally 8% trehalose is added as protectant before lyophilization.
Stability & Storage
Lyophilized powders can be stably stored for over 12 months, while liquid products can be stored for 6-12 months at -80°C. For reconstituted protein solutions, the solution can be stored at -20°C to -80°C for at least 3 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
ShippingIn general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.
Research Background
Acute kidney injury (AKI) is one of the most common complications of various serious conditions, and early diagnosis is therefore critical for the treatment of AKI. Recent evidence demonstrates that neutrophil gelatinase- associated lipocalin (NGAL) is closely associated with AKI. Several experimental and clinical studies have shown that the expression of urine and serum NGAL increases significantly in AKI. NGAL shows potential to be a new effective early biochemical marker of AKI. Further studies are needed to confirm the significant advantages of NGAL in the diagnosis of early AKI and its value in clinical applications.

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