NY-ESO-1 94-102 (HLA-B*35:01) (HLA-B*51:01) MPFATPMEA
€105.00*
Description
NY-ESO-1 94-102 (MPFATPMEA) is a specialized nonamer covering the sequence position 94-102 of the human Cancer/Testis Antigen 1 (NY-ESO-1; UniProt: P78358). This epitope is uniquely recognized by human CD8+ T-cells in the context of both HLA-B*35:01 and HLA-B*51:01 molecules.
Key Features:
- Dual HLA Restriction: Ideal for research involving diverse donor groups with B35 or B51 backgrounds.
- Single-Cell Analysis: Highly effective for the analysis and sorting of individual antigen-specific T-cells via multimer staining or functional assays.
- Immunodominant Region: Part of the high-density epitope cluster (aa 86-102), essential for comprehensive epitope mapping.
Applications:
- Identification and characterization of rare antigen-specific T-cell populations.
- Research into HLA cross-reactivity and MHC-peptide stability.
- Development of personalized immunotherapy protocols.
Explore the NY-ESO-1 86-102 Epitope Cluster
Depending on your HLA-restriction of interest, you might also consider:
- NY-ESO-1 86-94 (RLLEFYLAM) – Optimized for HLA-A*02:01
- NY-ESO-1_LAGE-2 91-101 (YLAMPFATPME) – Optimized for HLA-A*24:02
- NY-ESO-1 93-101 (AMPFATPME) – Optimized for HLA-B*07:02
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TechData
| Sequence: | MPFATPMEA |
| Gene: | CTAG1A |
| Delivery: | 3 weeks |
| C-Terminus: | OH |
| N-Terminus: | H |
| Amount: | 1 mg |
| Counterion: | TFA |
| Protein: | Cancer testis antigen, NY-ESO-1 |
| Species: | Human |
| Allele: | HLA-B*35:01, HLA-B*51:01 |
| Application: | Flow Cytometry |
| Indication: | Cancer |
| Purity: | 95% HPLC-MS |
Documents
References
Callahan, Margaret K et al. “Paradoxical activation of T cells via augmented ERK signaling mediated by a RAF inhibitor.” Cancer immunology research vol. 2,1 (2014): 70-9. doi:10.1158/2326-6066.CIR-13-0160
Sun, Zhaojun et al. “A new LAGE-1 peptide recognized by cytolytic T lymphocytes on HLA-A68 tumors.” Cancer immunology, immunotherapy : CII vol. 55,6 (2006): 644-52. doi:10.1007/s00262-005-0066-x
Lin, Yun et al. “Optimization and validation of a robust human T-cell culture method for monitoring phenotypic and polyfunctional antigen-specific CD4 and CD8 T-cell responses.” Cytotherapy vol. 11,7 (2009): 912-22. doi:10.3109/14653240903136987
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