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Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
Registration enables users to use special features of this website, such as past
order histories, retained contact details for faster checkout, review submissions, and special promotions.
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CD8
CD8 (cluster of differentiation 8) is a transmembrane glycoprotein that serves as a co-receptor for the T cell receptor (TCR). Like the TCR, CD8 binds to a major histocompatibility complex (MHC) molecule, but is specific for the class I MHC protein. There are two isoforms of the protein, alpha and beta, each encoded by a different gene. In humans, both genes are located on chromosome 2 in position 2p12. The CD8 co-receptor is predominantly expressed on the surface of cytotoxic T cells, but can also be found on natural killer cells, cortical thymocytes, and dendritic cells. It is expressed in T cell lymphoblastic lymphoma and hypo-pigmented mycosis fungoides. To function, CD8 forms a dimer, consisting of a pair of CD8 chains. The most common form of CD8 is composed of a CD8-alpha and CD8-beta chain, both members of the immunoglobulin superfamily with an immunoglobulin variable (IgV)-like extracellular domain connected to the membrane by a thin stalk, and an intracellular tail. Less-common homodimers of the CD8-alpha chain are also expressed on some cells.
Inhibition of adaptive immunity by IL9 can be disrupted to achieve rapid T-cell sensitization and rejection of progressive tumor challenges. Hoelzinger DB, Dominguez AL, Cohen PA, Gendler SJ. Cancer research. 2014 74:6845-55. (WB; Mouse)[Full Text Article]
[PubMed:25297635]
[PMC:PMC4254354]
2
A canine chimeric monoclonal antibody targeting PD-L1 and its clinical efficacy in canine oral malignant melanoma or undifferentiated sarcoma. Maekawa N, Konnai S, Takagi S, Kagawa Y, Okagawa T, Nishimori A, Ikebuchi R, Izumi Y, Deguchi T, Nakajima C, Kato Y, Yamamoto K, Uemura H, Suzuki Y, Murata S, Ohashi K. Scientific reports. 2017 7:8951. (Flo; Dog)[Full Text Article]
[PubMed:28827658]
[PMC:PMC5567082]
Related Antibodies: LS-C188088.
3
Systemic Blockade of Clever-1 Elicits Lymphocyte Activation Alongside Checkpoint Molecule Downregulation in Patients with Solid Tumors: Results from a Phase I/II Clinical Trial10<sup> Drug Development Unit, Royal Marsden NHS Foundation Trust/Institute of Cancer Research, Sutton, United Kingdom12<sup> Terveystalo Finland, Helsinki, Finland14<sup> MediCity Research Laboratory, University of Turku, Turku, Finland. maijal@utu.fi. Reetta Virtakoivu #, Jenna H Rannikko # , Miro Viitala # , Felix Vaura, Akira Takeda, Tapio Lönnberg, Jussi Koivunen, Panu Jaakkola, Annika Pasanen, Shishir Shetty, Maja J A de Jonge, Debbie Robbrecht, Yuk Ting Ma, Tanja Skyttä, Anna Minchom, Sirpa Jalkanen, Matti K Karvonen, Jami Mandelin, Petri Bono , Maija Hollmén. The Breast : official journal of the European Society of Mastology. 2021 Aug;27:4205-4220. [Full Text Article]
[PubMed:34078651]
Related Antibodies: LS-C311966.
4
Comparison of H7N9 and H9N2 influenza infections in mouse model unravels the importance of early innate immune response in host protection. Cuisong Zhu, Miaomiao Zhang, Weihui Fu, Yongquan He, Yu Yang, Linxia Zhang, Songhua Yuan, Lang Jiang, Jianqing Xu, Xiaoyan Zhang. Frontiers in cellular and infection microbiology. 2022 August;12:941078. [Full Text Article]
[PubMed:36034707]
[PMC:PMC9414078]
Related Antibodies: LS-C43572.
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PLEASE NOTE
For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.
The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).