PROVETOP

Human GITR/TNFRSF18 Protein, Ultra Low Endotoxin

Catalog No: GITR-HP003

Species
Human
Expression System
HEK293
Tag
an hFc (IgG1)
Activity
Activity verified

Product overview

Recombinant Human GITR/TNFRSF18 Protein is expressed in HEK293 cells with an hFc (IgG1) tag at the C-terminus. It contains amino acid residues Gln26-Glu161 (UniProt accession: Q9Y5U5-1).

Product Details

Molecular Aliases
CD357; GITR; GITR-D; TNFRSF18; AITR
Protein Length
Gln26-Glu161
Expression System
HEK293
Theoretical Molecular Weight
The protein has a predicted MW of 41.3 kDa. Due to glycosylation, the protein migrates to 45-55 kDa based on Bis-Tris PAGE result.
Purity
> 95% as determined by Bis-Tris PAGE > 95% as determined by HPLC
Endotoxin
Less than 0.01 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
GITR-HP003 Bis-Tris-PAGE-white result

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

SEC-HPLC
GITR-HP003 SEC-HPLC result

The purity of Human GITR is greater than 95% as determined by SEC-HPLC.

ELISA
GITR-HP003 ELISA result

Immobilized Human GITR Ligand Trimer, His Tag at 5μg/ml (100μl/well) on the plate. Dose response curve for Human GITR, hFc Tag with the EC50 of 50.8ng/ml determined by ELISA.

Background

GITR (glucocorticoid-induced tumor necrosis factor receptor), also known as AITR and TNFRSF18, is a 40 kDa transmembrane glycoprotein that functions in immune regulation.GIRT is a receptor for TNFSF18. Seems to be involved in interactions between activated T-lymphocytes and endothelial cells and in the regulation of T-cell receptor-mediated cell death. Mediated NF-kappa-B activation via the TRAF2/NIK pathway.

References

  1. Knee D A, Hewes B, Brogdon J L. Rationale for anti-GITR cancer immunotherapy[J]. European Journal of Cancer, 2016, 67:1-10. Note: HPLC results always come from liquid protein, due to absorption peak interference of trehalose in lyophilized powder.

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