Anti-Human PD-L1 (CD274) (Clone 29E.2A3) – Biotin
Anti-Human PD-L1 (CD274) (Clone 29E.2A3) – Biotin
Product No.: P604
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Clone 29E.2A3 Target PD-L1 Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names CD274, B7-H1, Programmed death-ligand 1 Isotype Mouse IgG2b κ Applications FC |
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Antibody DetailsProduct DetailsReactive Species Human Host Species Mouse Immunogen Full length Human PD-L1 Product Concentration 0.5 mg/ml Formulation This Biotinylated antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.4, 1% BSA and 0.09% sodium azide as a preservative. State of Matter Liquid Product Preparation Functional grade preclinical antibodies are manufactured in an animal free facility using only In vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling This biotinylated antibody is stable when stored at 2-8°C. Do not freeze. Regulatory Status Research Use Only Country of Origin USA Shipping 2-8°C Wet Ice Additional Applications Reported In Literature ? FC Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity Human PD-L1 (CD274) Background Programmed cell death 1 ligand 1 (PD-L1; CD274; B7-H1) is a type I transmembrane glycoprotein widely expressed in many types of tissues that acts as a ligand for the immune inhibitory receptor programmed cell death 1 (PD-1; CD279)1, 2, 3. The PD-1 pathway is responsible for T cell activation, proliferation, and cytotoxic secretion, with PD-1/PD-L1 interaction triggering inhibitory signals that dampen T cell function. PD-L1 also plays a critical role in the differentiation of inducible regulatory T cells4. In normal tissues, PD-L1/PD-1 ligation is crucial to maintaining homeostasis of the immune system and preventing autoimmunity during infection and inflammation4. In the tumor microenvironment, their interaction provides an immune escape mechanism for tumor cells by turning off cytotoxic T cells. As such, blocking the PD-L1/PD-1 interaction is a target of many anti-cancer immunotherapies. 29E.2A3 was generated by immunizing female BALB/c mice with purified hPD-L1 cDNA5. Spleen cells were fused with SP2/0 myeloma cells, and the resulting hybridomas were screened by ELISA for reactivity against hPD-L1–Ig fusion protein followed by cell-surface staining of hPD-L1–transfected Chinese hamster ovary cells and 300.19 cells. Antigen Distribution PD-L1 is commonly expressed on the surface of antigen presenting cells (macrophages, activated B cells, dendritic cells), some epithelial cells under inflammatory conditions, some activated T cells, and several types of tumors as well as tumor infiltrating immune cells. PD-L1 can also exist in a soluble form (sPD-L1) in myeloid-derived cells (monocytes, macrophages, and dendritic cells) and several human cancer lines. Ligand/Receptor PD-1 (CD279) NCBI Gene Bank ID UniProt.org Research Area Apoptosis . Cancer . Cell Biology . Cell Death . Immunology . Inhibitory Molecules . Tumor Suppressors References & Citations1. Freeman GJ, Long AJ, Iwai Y, et al. J Exp Med. 2000192(7):1027-1034. 2000. 2. Tsai KK, Zarzoso I, Daud AI. Hum Vaccin Immunother. 10(11):3111-3116. 2014. 3. Han Y, Liu D, Li L. Am J Cancer Res. 10(3):727-742. 2020. 4. Dermani FK, Samadi P, Rahmani G, et al. J Cell Physiol. 234(2):1313-1325. 2019. 5. Latchman Y, Wood CR, Chernova T, et al. Nat Immunol. 2(3):261-268. 2001. 6. Brown JA, Dorfman DM, Ma FR, et al. J Immunol. 170(3):1257-1266. 2003. 7. Cai G, Karni A, Oliveira EM, et al. Cell Immunol. 230(2):89-98. 2004. 8. Porichis F, Hart MG, Zupkosky J, et al. J Virol. 88(5):2508-2518. 2014. 9. Hughes MJ, McGettrick HM, Sapey E. J Immunol Methods. 483:112795. 2020. 10. Boyerinas B, Jochems C, Fantini M, et al. Cancer Immunol Res. 3(10):1148-1157. 2015. 11. Nakamoto N, Cho H, Shaked A, et al. PLoS Pathog. 5(2):e1000313. 2009. 12. Hegde S, Lockridge JL, Becker YA, et al. J Autoimmun. 37(1):28-38. 2011. 13. Broos K, Lecocq Q, Keersmaecker B, et al. Vaccines (Basel). 7(3):85. 2019. 14. Darga EP, Dolce EM, Fang F, et al. PLoS One. 16(11):e0260124. 2021. Technical ProtocolsCertificate of Analysis |
Formats Available
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Prod No. | Description |
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P604 | |
P611 | |
P609 | |
P610 | |
P602 | |
P605 | |
P606 | |
P607 | |
P608 | |
P603 |
