Recombinant Human IL-21 GMP Protein, CF
R&D Systems | Catalog # 8879-GMP
Key Product Details
Source
Accession Number
Applications
Product Specifications
Source
Gln32-Ser162, with a N-terminal Met
Produced in an animal-free laboratory. Manufactured and tested under cGMP guidelines
Purity
Endotoxin Level
N-terminal Sequence Analysis
Met-Gln-Asp-Arg-His-Met-Ile-Arg-Met-Arg
Predicted Molecular Mass
SDS-PAGE
Activity
The ED50 for this effect is 5.00-50.0 ng/mL.
The specific activity of recombinant human IL-21 is >1.00 x 106 units/mg, which is calibrated against an internal reference standard for human IL-21.
Measured by its ability to enhance IFN-gamma secretion in NK-92 human natural killer lymphoma cells.
The ED50 for this effect is ≤8 ng/mL.
Host Cell Protein
Mycoplasma
Scientific Data Images for Recombinant Human IL-21 GMP Protein, CF
Recombinant Human IL‑21 GMP Protein Bioactivity.
Recombinant Human IL‑21 GMP (Catalog # 8879-GMP) induces B9 mouse hybridoma cell proliferation. The ED50 for this effect is 5.00-50.0 ng/mLRecombinant Human IL-21 GMP Protein Bioactivity
GMP-grade Recombinant Human IL-21 (Catalog # 8879‑GMP) enhances IFN-gamma secretion in NK-92 human natural killer lymphoma cells. The ED50 for this effect is ≤8 ng/mL. Three independent lots were tested for activity and plotted on the same graph to show lot-to-lot consistency of GMP IL-21.Recombinant Human IL-21 GMP Protein SDS-PAGE
2 μg/lane of GMP-grade Recombinant Human IL-21 (Catalog # 8879-GMP) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, showing R band at 16.4 kDa and NR band at 14.8 kDa, respectively.Formulation, Preparation, and Storage
8879-GMP
| Formulation | Lyophilized from a 0.2 μm filtered solution in PBS. |
| Reconstitution | Reconstitute at 100-200 μg/mL in PBS. |
| Shipping | The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below. |
| Stability & Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
|
Calculators
Background: IL-21
References
- Tangye, S.G. (2015) Curr. Opin. Immunol. 34:107.
- Parrish-Novak, et al. (2000) Nature 408:57.
- Coquet, J.M. et al. (2007) J. Immunol. 178:2827.
- Vogelzang, A. et al. (2008) Immunity 29:127.
- Korn, T. et al. (2007) Nature 448:484.
- Nurieva, R. et al. (2007) Nature 448:480.
- Asao, H. et al. (2001) J. Immunol. 167:1.
- Zotos, D. et al. (2010) J. Exp. Med. 207:365.
- Rankin, A.L. et al. (2011) J. Immunol. 186:667.
- Jin, H. et al. (2009) J. Clin. Invest. 119:47.
- Frohlich, A. et al. (2009) Science 324:1576.
- Yi, J.S., et al. (2009) Science 324:1572.
- Peluso, I. et al. (2007) J. Immunol. 178:732.
- Bucher, C. et al. (2009) Blood 114:5375.
- Kasaian, M.T. et al. (2002) Immunity 16:559.
- Tamagawa-Mineoka, R. et al. (2011) J. Invest. Dermatol. 131:1513.
- Ma, J. et al. (2011) Cytokine 56:133.
- Rahman, M. et al. (2007) FEBS Lett. 581:4001.
Long Name
Alternate Names
Gene Symbol
UniProt
Additional IL-21 Products
Product Documents for Recombinant Human IL-21 GMP Protein, CF
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Manufacturing Specifications
GMP ProteinsR&D Systems, a Bio-Techne Brand's GMP proteins are produced according to relevant sections of the following documents: USP Chapter 1043, Ancillary Materials for Cell, Gene and Tissue-Engineered Products and Eu. Ph. 5.2.12, Raw Materials of Biological Origin for the Production of Cell-based and Gene Therapy Medicinal Products.
R&D Systems' quality focus includes:
- Designed, manufactured and tested under an ISO 9001:2015 and ISO 13485:2016 certified quality system
- Documented and controlled manufacturing process
- Control of documentation and process changes by QA
- Personnel training programs
- Raw material inspection and vendor qualification/monitoring program
- Validated equipment, processes and test methods
- Equipment calibration and maintenance schedules using a Regulatory Asset Manager
- Facility/Utilities maintenance, contamination controls, safety and pest control programs
- Material review process for variances
- Robust product stability program following relevant ICH guidelines
- N-terminal amino acid analysis
- SDS-PAGE purity analysis
- Molecular weight analysis via mass spectrometry
- Endotoxin assessment per USP <85> and Ph. Eur. 2.6.14 guidelines
- Bioassay analysis
- Microbial testing per USP <71> and Ph. Eur. 2.6.1 guidelines
- Host cell protein assessment
- Host cell DNA assessment
- Mycoplasma assessment
Production records and facilities are available for examination by appropriate personnel on-site at R&D Systems in Minneapolis and St. Paul, Minnesota USA.
R&D Systems sells GMP grade products for preclinical or clinical ex vivo use. They are not for in vivo use. Please read the following End User Terms prior to using this product.
Animal-Free Manufacturing Conditions
Our dedicated controlled-access animal-free laboratories ensure that at no point in production are the products exposed to potential contamination by animal components or byproducts. Every stage of manufacturing is conducted in compliance with R&D Systems' stringent Standard Operating Procedures (SOPs). Production and purification procedures use equipment and media that are confirmed animal-free.
Production
- All molecular biology procedures use animal-free media and dedicated labware.
- Dedicated fermentors are utilized in committed animal-free areas.
- Protein purification columns are animal-free.
- Bulk proteins are filtered using animal-free filters.
- Purified proteins are stored in animal-free containers.
Product Specific Notices for Recombinant Human IL-21 GMP Protein, CF
Full terms and conditions of sale can be found online in the Protein Sciences Segment T&Cs at: Terms & Conditions.
For preclinical, or clinical ex vivo use
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FAQs for Recombinant Human IL-21 GMP Protein, CF
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Q: What are the units of activity for Recombinant Human IL-21 GMP Protein, CF GMP (Catalog # 8879-GMP)?
A: Currently, no NIBSC reference standard is available for human IL-21, so we do not have a unit conversion factor available for Recombinant Human IL-21 GMP Protein, CF GMP (Catalog # 8879-GMP). We recommend checking the Citations tab on the product-specific page to review publications citing use of the product. We would also recommend peforming a dose-response study for your assay to determine the optimal concentration for your experiment. If you need additional assistance determining how to use the protein in your application, please contact Technical Support.