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anti-Mouse (Murine) CD8 Antibodies:
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Mouse (Murine) Monoclonal CD8 Primary Antibody for BR, Func - ABIN1177008
Anel, ORourke, Kleinfeld, Mescher: T cell receptor and CD8-dependent tyrosine phosphorylation events in cytotoxic T lymphocytes: activation of p56lck by CD8 binding to class I protein. in European journal of immunology 1996
Show all 25 Pubmed References
Mouse (Murine) Monoclonal CD8 Primary Antibody for BR, IHC (f) - ABIN2689432
Alexander-Miller, Leggatt, Sarin, Berzofsky: Role of antigen, CD8, and cytotoxic T lymphocyte (CTL) avidity in high dose antigen induction of apoptosis of effector CTL. in The Journal of experimental medicine 1996
Show all 24 Pubmed References
Mouse (Murine) Monoclonal CD8 Primary Antibody for FACS, Sep - ABIN2689436
Bierer, Sleckman, Ratnofsky, Burakoff: The biologic roles of CD2, CD4, and CD8 in T-cell activation. in Annual review of immunology 1989
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Rat (Rattus) Monoclonal CD8 Primary Antibody for BR, IAC - ABIN967471
Barclay: The localization of populations of lymphocytes defined by monoclonal antibodies in rat lymphoid tissues. in Immunology 1981
Show all 16 Pubmed References
Human Monoclonal CD8 Primary Antibody for ICC, FACS - ABIN268292
Sroga, Jones, Kigerl, McGaughy, Popovich: Rats and mice exhibit distinct inflammatory reactions after spinal cord injury. in The Journal of comparative neurology 2003
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Rat (Rattus) Monoclonal CD8 Primary Antibody for BR, IAC - ABIN2689435
Brideau, Carter, McMaster, Mason, Williams: Two subsets of rat T lymphocytes defined with monoclonal antibodies. in European journal of immunology 1980
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Mouse (Murine) Monoclonal CD8 Primary Antibody for FACS, Func - ABIN349708
Bouwer, Alberti-Segui, Montfort, Berkowitz, Higgins: Directed antigen delivery as a vaccine strategy for an intracellular bacterial pathogen. in Proceedings of the National Academy of Sciences of the United States of America 2006
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Mouse (Murine) Monoclonal CD8 Primary Antibody for IHC (f), IHC (fro) - ABIN2689434
Sydora, Brossay, Hagenbaugh, Kronenberg, Cheroutre: TAP-independent selection of CD8+ intestinal intraepithelial lymphocytes. in Journal of immunology (Baltimore, Md. : 1950) 1996
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Mouse (Murine) Monoclonal CD8 Primary Antibody for CyTOF, Dep - ABIN4295972
Fazio, Zappulla, Notartomaso, Busceti, Bessede, Scarselli, Vacca, Gargaro, Volpi, Allegrucci, Lionetto, Simmaco, Belladonna, Nicoletti, Fallarino: Cinnabarinic acid, an endogenous agonist of type-4 metabotropic glutamate receptor, suppresses experimental autoimmune encephalomyelitis in mice. in Neuropharmacology 2014
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Rat (Rattus) Monoclonal CD8 Primary Antibody for FACS, Func - ABIN1027698
Pino, OSullivan-Murphy, Lidstone, Yang, Lipson, Jurczyk, diIorio, Brehm, Mordes, Greiner, Rossini, Bortell: CHOP mediates endoplasmic reticulum stress-induced apoptosis in Gimap5-deficient T cells. in PLoS ONE 2009
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results suggest that CD4 CD8 double knockout (DN)T cells can develop efficiently in vivo and chronic exposure to bacterial superantigens may precipitate a lupus-like autoimmune disease through activation of DNT cells
Depletion of Depletion of medullary thymic epithelial cells (mTECs) and CD8 antigen alpha chain (CD8alpha+) dendritic cells (DCs) leads to overt autoimmunity.
The generation of cancer-specific CD8(+) CD69(+)-expressing lymphocytes that inhibit colon cancer growth has been described.
TCF-1-deficient CD4+ CD8+ double positive thymocytes fail to undergo TCR alpha Valpha14-Jalpha18 rearrangement and produce significantly fewer Natural killer T cells.
Batf3 deficiency is not critical for the generation of CD8alpha dendritic cells
Lck-CD8 interaction is required for initial CD8 recruitment.
Brd1-mediated Hbo1 activity is crucial for efficient activation of CD8 expression via acetylation at H3K14, which serves as an epigenetic mark that promotes the recruitment of transcription machinery to the CD8 enhancers.
Ly49E is expressed on a high proportion of CD8alphaalpha-positive intestinal intraepithelial lymphocytes.
Comparing the sequences of mouse, human, rat and dog Cd8a and Cd8b1 gene loci identified 10 evolutionarily conserved regions (ECR). 6 ECRs overlapped with previously identified Cd8 enhancers. ECR-4 recruits transcription factors to the Cd8ab gene complex.
Data indicate that orphan G-protein-coupled receptor GPR18 is required for the normal homeostasis of CD8alphaalpha gammadeltaT and alphabetaT and CD8alphabeta intestinal intraepithelial lymphocyte compartment.
CD8alpha DCs, rather than CD8 T cells, are responsible for enhanced viral latency and recurrences.
Data show that targeting nanoparticles containing alpha-galactosylceramide (alpha-GalCer) and Ag to CD8alpha(+) dendritic cells promotes potent antitumor responses, both in prophylactic and in therapeutic settings.
Downregulation of CD8 during type 2 olarization of murine CD8(+) effector T cells is associated with CpG methylation of several regions of the Cd8a locus.
Data indicate that CD8alpha knockout mice reconstituted with CD8(+) T cells restored the sensitivity to Ang II.
CREMalpha orchestrates epigenetic remodeling of the CD8A,B through the recruitment of DNA methyltransferase (DNMT) 3a and histone methyltransferase G9a.
Therefore, EXOs derived from natural CD4(+)25(+) and CD8(+)25(+) Tr cells may become an alternative for immunotherapy of autoimmune diseases.
Data indicate that CD8low cells survive long term in vivo.
A previously undescribed pathway by which CD8alpha+ Dendritic cells emerge independent of Id2, Nfil3, and Batf3, but dependent on Irf8.
Age-associated alterations in CD8alpha+ dendritic cells impair CD8 T-cell expansion in response to an intracellular bacterium.
During establishment of viral persistence, the cellular subset with the most prevalent expression of IL-10 was CD8alpha(-)CD4(+) dendritic cells (DCs), which produced IL-10 with increasing kinetics until 9 d postinfection.
High CD8 expression is associated with gastric Cancer.
Studied lymphocyte phenotype in resected lymph nodes of patients with lung cancer by analyzing levels of Foxp3 and CD8 by immunohistochemical staining.
This study compares the differences of PD-L1 expression and CD8+ tumor-infiltrating lymphocyte density, two major response biomarkers of PD-1/PD-L1 blockade, between paired primary and brain metastatic lesions in advanced non-small cell lung cancer (NSCLC). For NSCLC brain metastases patients, CD8+ tumor-infiltrating lymphocyte density showed a spatial and temporal heterogeneity.
Long-term lung function decline in asthma is associated with elevation of bronchial CD8 and CD4 at baseline, and CD8, CD3 and granzyme B at follow-up
Endometrioid endometrial carcinomas are capable of down-regulating CD8 expression by cytotoxic T lymphocytes.
The PD-1/CD8 ratio may, therefore, be a useful prognostic marker for stage II/III CRC. What is important for predicting the prognosis may be the PD-1/CD8 ratio rather than the absolute number of PD-1(+) tumor-infiltrating lymphocytes .
We also observed a significant association between forkhead box protein 3 ( p = 0.001) and the Neo-Bioscore, while only a marginal difference was observed with CD8+ expression ( p = 0.074). This study demonstrated that forkhead box protein 3 expression has value as the only independent marker that predicts a good response to neoadjuvant chemotherapy and that it is related with a good prognosis according to the Neo-Biosc
missense mutation increases susceptibility to recurrent respiratory infections
Human mesenchymal stromal cells enhance the immunomodulatory function of CD8(+)CD28(-) regulatory T cells.
In localized colorectal cancer carriers, mRNA-based CD3Z/CD8 profiling of tumor immune response may have stage, site and tissue-specific prognostic significance, along with ESR1 expression.
Dendritic cells accumulate in the bone marrow of multiple myeloma patients and protect tumor plasma cells from CD8+ T-cell killing.
Patients with the presence of CD8- and CD45RO-positive T cells in bone marrow demonstrated better survival of gastric cancer patients than those with the absence of these cells in bone marrow.
CD58/CD2 is the primary costimulatory pathway in human CD28-CD8+ T cells.
We suggest that unique set of interactions between CEACAM5, CD1d, and CD8 render CD1d more class I-like molecule, facilitating antigen presentation and activation of CD8(+)-suppressor regulatory T cells.
More sCD8 circulating molecules were found in patients transfused with post-storage leucodepleted RBCs whose supernatants had large amounts of sHLA-I. sCD8 is a possible modulator of sHLA-I-mediated transfusion-related immunomodulation.
CD8-positivity proved to be an independent prognostic predictor of worse outcome in pediatric anaplastic lymphoma kinase-positive anaplastic large cell lymphoma.
Modified CD8A gene function may contribute to the development of refractory chronic rhinosinusitis via reduction of circulating CD8 lymphocytes.
transcription factor cAMP-responsive element modulator alpha (CREMalpha), which is expressed at increased levels in T cells from systemic lupus erythematosus patients, contributes to transcriptional silencing of CD8A and CD8B.
The CD8(+)CCR7(+) T-cell frequency in HNSCC patients' blood tested at diagnosis can discriminate them from normal controls and predicts disease recurrence
Findings indicate associations of differentiation 8 alpha (CD8A) variants with T lymphocyte subpopulations and suggest applications in porcine breeding programs.
Crystallographic analysis of swine CD8alpha (sCD8alpha) to 1.8 A resolution revealed that the crystals belonged to space group P3(2)21, with unit-cell parameters a = 80.97, b = 80.97, c = 95.19 A
The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen acts as a coreceptor with the T-cell receptor on the T lymphocyte to recognize antigens displayed by an antigen presenting cell in the context of class I MHC molecules. The coreceptor functions as either a homodimer composed of two alpha chains or as a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 alpha chain. Multiple transcript variants encoding different isoforms have been found for this gene.
, CD8a molecule
, T-cell surface glycoprotein CD8 alpha chain
, CD8 antigen, alpha polypeptide
, T-cell surface glycoprotein CD8 alpha chain-like
, Lyt-2.1 lymphocyte differentiation antigen (AA at 100)
, T-cell surface glycoprotein Lyt-2
, CD8 antigen, alpha polypeptide (p32)
, Leu2 T-lymphocyte antigen
, OKT8 T-cell antigen
, T cell co-receptor
, T-cell antigen Leu2
, T-lymphocyte differentiation antigen T8/Leu-2
, T8 T-cell antigen
, CD8 antigen 32 kDa chain
, CD8 antigen alpha-chain
, CD8 antigen, alpha chain
, CD8 antigen, alpha-chain
, OX-8 membrane antigen
, CD8 antigen alpha polypeptide
, CD8 alpha chain
, T-cell surface molecule
, CD8 alpha molecule