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Recombinant Mouse Fas Ligand/TNFSF6 Protein, CF

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Product Details

Summary
Reactivity MuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

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Recombinant Mouse Fas Ligand/TNFSF6 Protein, CF Summary

Details of Functionality
Measured by its ability to induce apoptosis of Jurkat human acute T cell leukemia cells. The ED50 for this effect is 1-8 ng/mL in the presence of 2.5 µg/mL of a cross-linking antibody, Mouse Anti-Hemagglutinin/HA Peptide Monoclonal Antibody (Catalog # MAB060).
Source
Chinese Hamster Ovary cell line, CHO-derived mouse Fas Ligand/TNFSF6 protein
Hemagglutinin Tag 
(YPYDVPDYA)
GCN4-IZ (GGGS)3 Mouse Fas Ligand
(Gln101-Leu279)
Accession # P41047
N-terminus C-terminus
Accession #
N-terminal Sequence
Tyr
Protein/Peptide Type
Recombinant Proteins
Gene
Fasl
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<0.01 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
25.9 kDa (monomer).
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
40-55 kDa, reducing conditions
Publications
Read Publication using
6128-SA/CF in the following applications:

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 100 μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Mouse Fas Ligand/TNFSF6 Protein, CF

  • apoptosis (APO-1) antigen ligand 1
  • Apoptosis antigen ligand
  • APT1LG1CD95L
  • APTL
  • CD178 antigen
  • CD178
  • CD95L
  • CD95-L
  • Fas antigen ligand
  • Fas ligand (TNF superfamily, member 6)
  • Fas Ligand
  • FASLCD95 ligand
  • FASLG
  • TNFSF6
  • TNFSF6FasL
  • tumor necrosis factor (ligand) superfamily, member 6
  • tumor necrosis factor ligand superfamily member 6

Background

Fas Ligand (FasL), also known as CD178, CD95L, or TNFSF6, is a 40 kDa type II transmembrane member of the TNF superfamily of proteins. Its ability to induce apoptosis in target cells plays an important role in the development, homeostasis, and function of the immune system (1). Mature mouse Fas Ligand consists of a 179 amino acid (aa) extracellular domain (ECD), a 22 aa transmembrane segment, and a 78 aa cytoplasmic domain (2). Within the ECD, mouse Fas Ligand shares 81% and 93% aa sequence identity with human and rat Fas Ligand, respectively. Alternate splicing generates a 16 kDa isoform that corresponds to the C-terminal 69 amino acids of the ECD (3). Both mouse and human Fas Ligand are active on mouse and human cells (4, 5). Fas Ligand is expressed as a nondisulfide-linked homotrimer on activated CD4+ Th1 cells, CD8+ cytotoxic T cells, and NK cells (1). Fas Ligand binding to Fas/CD95 on an adjacent cell triggers apoptosis in the Fas‑expressing cell (2, 4). Fas Ligand also binds DcR3 which is a soluble decoy receptor that interferes with Fas Ligand-induced apoptosis (6). Fas Ligand can be released from the cell surface by metalloproteinases as a 26 kDa soluble molecule which remains trimeric (7, 8). Shed Fas Ligand retains the ability to bind Fas, although its ability to trigger apoptosis is dramatically reduced (7, 8). In the absence of TGF‑ beta , however, Fas Ligand/Fas interactions instead promote neutrophil-mediated inflammatory responses (5, 9). Fas Ligand itself transmits reverse signals that costimulate the proliferation of freshly antigen-stimulated T cells (10). Fas Ligand‑induced apoptosis plays a central role in the development of immune tolerance and the maintance of immune privileged sites (11). This function is exploited by tumor cells which evade immune surveillance by upregulating Fas Ligand to kill tumor infiltrating lymphocytes (9, 12). In gld mice, a Fas Ligand point mutation is the cause of severe lymphoproliferation and systemic autoimmunity (13, 14).

  1. Lettau, M. et al. (2008) Curr. Med. Chem. 15:1684.
  2. Suda, T. et al. (1993) Cell 75:1169.
  3. Ayroldi, E. et al. (1999) Blood 94:3456.
  4. Takahashi, T. et al. (1994) Int. Immunol. 6:1567.
  5. Seino, K-I. et al. (1998) J. Immunol. 161:4484.
  6. Pitti, R.M. et al. (1998) Nature 396:699.
  7. Schneider, P. et al. (1998) J. Exp. Med. 187:1205.
  8. Tanaka, M. et al. (1998) Nature Med. 4:31.
  9. Chen, J.-J. et al. (1998) Science 282:1714.
  10. Suzuki, I. and P.J. Fink (2000) Proc. Natl. Acad. Sci. 97:1707.
  11. Ferguson, T.A. and T.S. Griffith (2006) Immunol. Rev. 213:228.
  12. Ryan, A.E. et al. (2005) Cancer Res. 65:9817.
  13. Takahashi, T. et al. (1994) Cell 76:969.
  14. Lynch, D.H. et al. (1994) Immunity 1:131.

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Publications for Fas Ligand/TNFSF6 (6128-SA/CF)(1)

We have publications tested in 1 confirmed species: Mouse.

We have publications tested in 1 application: Bioassay.


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Bioinformatics

Gene Symbol Fasl
Uniprot