PROVETOP

Human FGF21 Protein

Catalog No: FGF21-HP002

Species
Human
Expression System
HEK293
Tag
His
Activity
Activity verified

Product overview

Recombinant Human FGF21 Protein is expressed in HEK293 cells with a His tag at the N-terminus. It contains amino acid residues His29-Ser209 (UniProt accession: Q9NSA1-1).

Product Details

Molecular Aliases
UNQ3115; PRO10196; FGF-21; FGF21
Protein Length
His29-Ser209
Expression System
HEK293
Theoretical Molecular Weight
The protein has a predicted MW of 20.2 kDa. Due to glycosylation, the protein migrates to 25-30 kDa based on Bis-Tris PAGE result.
Purity
> 95% as determined by Bis-Tris PAGE
Endotoxin
Less than 1 EU per μg by the LAL method.
Buffer / Formulation
Lyophilized from 0.22μm filtered solution in PBS (pH 7.4). Normally 8% trehalose is added as protectant before lyophilization.
State
Lyophilized
Storage Conditions
-20 to -80°C for 12 months as supplied from date of receipt. -80°C for 3 months after reconstitution. Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles.
Reconstitution Advice
Dissolve the lyophilized protein in distilled water. Please refer to the Certificate of Analysis for detailed instructions.

Data Display

Bis-Tris PAGE
FGF21-HP002 Bis-Tris-PAGE-white result

Human FGF21 on Bis-Tris PAGE under reduced condition. The purity is greater than 95%.

SPR
FGF21-HP002 SPR result

Human FGF21, His Tag immobilized on CM5 Chip can bind Human Beta Klotho, His Tag with an affinity constant of 20nM as determined in a SPR assay (Biacore T200).

Background

Fibroblast growth factor 21 (FGF21) is a peptide hormone that is synthesized by several organs and regulates energy homeostasis. Excitement surrounding this relatively recently identified hormone is based on the documented metabolic beneficial effects of FGF21, which include weight loss and improved glycemia.

References

  1. Lewis JE, Ebling FJP, Samms RJ, Tsintzas K. Going Back to the Biology of FGF21: New Insights. Trends Endocrinol Metab. 2019;30(8):491-504. doi:10.1016/j.tem.2019.05.007

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