Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Human CD247 Antibodies:
anti-Mouse (Murine) CD247 Antibodies:
anti-Rat (Rattus) CD247 Antibodies:
Go to our pre-filtered search.
Mouse (Murine) Monoclonal CD247 Primary Antibody for CyTOF, FACS - ABIN4900709
Jones, Stumhofer, Foster, Twohig, Hertzog, Topley, Williams, Hunter, Jenkins, Wang, Jones: Naive and activated T cells display differential responsiveness to TL1A that affects Th17 generation, maintenance, and proliferation. in FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2011
Show all 8 Pubmed References
Mouse (Murine) Monoclonal CD247 Primary Antibody for CyTOF, FACS - ABIN4900705
Vang, Housley, Dong, Basole, Ben-Sasson, Kream, Epstein, Clark, Brocke: Regulatory T-cells and cAMP suppress effector T-cells independently of PKA-CREM/ICER: a potential role for Epac. in The Biochemical journal 2013
Show all 7 Pubmed References
Human Monoclonal CD247 Primary Antibody for FACS, IF - ABIN965779
Dumont, Blanchard, Di Bartolo, Lezot, Dufour, Jauliac, Hivroz: TCR/CD3 down-modulation and zeta degradation are regulated by ZAP-70. in Journal of immunology (Baltimore, Md. : 1950) 2002
Show all 4 Pubmed References
Human Monoclonal CD247 Primary Antibody for ICC, FACS - ABIN1724734
Nambiar, Fisher, Warke, Krishnan, Mitchell, Delaney, Tsokos: Reconstitution of deficient T cell receptor zeta chain restores T cell signaling and augments T cell receptor/CD3-induced interleukin-2 production in patients with systemic lupus erythematosus. in Arthritis and rheumatism 2003
Show all 3 Pubmed References
Mouse (Murine) Monoclonal CD247 Primary Antibody for FACS - ABIN4898316
Lin, Xu, Jin, Zhong, Di, Lin: CXCL12 enhances exogenous CD4+CD25+ T cell migration and prevents embryo loss in non-obese diabetic mice. in Fertility and sterility 2009
Show all 2 Pubmed References
Human Monoclonal CD247 Primary Antibody for ICC, FACS - ABIN2749060
Dopfer, Schöpf, Louis-Dit-Sully, Dengler, Höhne, Klescová, Prouza, Suchanek, Reth, Schamel: Analysis of novel phospho-ITAM specific antibodies in a S2 reconstitution system for TCR-CD3 signalling. in Immunology letters 2010
Human Monoclonal CD247 Primary Antibody for ICS - ABIN1177045
Alberola-Ila, Takaki, Kerner, Perlmutter: Differential signaling by lymphocyte antigen receptors. in Annual review of immunology 1997
Mouse (Murine) Monoclonal CD247 Primary Antibody for FACS - ABIN4898308
Lemay, Rintoul, Kus, Paterson, Garcia, Falls, Ferreira, Bridle, Conrad, Tang, Diallo, Arulanandam, Le Boeuf, Garson, Vanderhyden, Stojdl, Lichty, Atkins, Parato, Bell, Auer: Harnessing oncolytic virus-mediated antitumor immunity in an infected cell vaccine. in Molecular therapy : the journal of the American Society of Gene Therapy 2012
analysis of the assembly and surface expression of FcepsilonR1alpha in cells shows that CD16A associates equally well with human CD247 and FcepsilonR1gamma homodimers
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
Crk-dependent increased phosphorylation of CD3zeta coincided with inhibition of TCR downmodulation, supporting a positive role for Crk adaptor proteins in TCR-mediated signal amplification.
the immunohistochemical staining patterns of CD3 (show CD3 Antibodies) and CD20 (show MS4A1 Antibodies) in Malignant Lymphoma Cells, were investigated.
CD274 (show CD274 Antibodies) up-regulation in new-onset type 1 diabetes mellitusis correlated with disease pathogenesis.
our observations suggested that CD247 gene polymorphism (rs858554) may associated with the susceptibility of RA.
CD3 (show CD3 Antibodies)/28-activated T cells expanded in IL-7 (show IL7 Antibodies) and IL-15 (show IL15 Antibodies) produced greater expansion of memory stem T cells and central memory T cell-derived T cells compared with IL-2 (show IL2 Antibodies). Our strategy provides a powerful tool to elucidate the characteristics of CAR-modified T cells, regardless of the protocol used for expansion, reveals the functional properties of each expanded T cell subset.
Multiple mutations were found in CD247 complementary DNAs (cDNAs) cloned from the patient as well as in cDNA and genomic DNA from other individuals, suggesting that genetic variation in this gene is frequent.
Single-nucleotide polymorphism in CD247 gene is associated with sclerotic graft-versus-host disease.
CD3Z hypermethylation was significantly correlated with SLE. CD3Z hypermethylation is an SLE risk factor that can be modified by environmental factors and is associated with more severe SLE clinical manifestations, which are related to deranged T cell function by downregulating the CD3zeta-chain.
ITAM sequence diversity is required for optimal TCR signal transduction and subsequent T cell maturation
Comprehensive Survey of miRNA-mRNA Interactions Reveals That Ccr7 (show CCR7 Antibodies) and Cd247 (CD3 zeta) are Posttranscriptionally Controlled in Pancreas Infiltrating T Lymphocytes of Non-Obese Diabetic (NOD) Mice
There is an early (within seconds) interaction between CD3zeta and the coreceptor CD8 that is independent of the binding of CD8 to MHC.
The resting TCR localized in the disordered domain of giant plasma membrane (PM) vesicles (GPMVs) and PM spheres (PMSs) and single and nanoclustered TCRs are found in the high-density fractions in sucrose gradients.
When Ly108 (show SLAMF6 Antibodies) is engaged in trans during cell-cell interactions, Ly108 (show SLAMF6 Antibodies)-CD3zeta interactions are promoted in a manner that uniquely depends on Ly108 (show SLAMF6 Antibodies) TM domain, leading to more efficient CD3zeta dephosphorylation.
Two transcription factor binding sites and a long non-coding RNA are identified within the Cd247 gene.
Zfat (show ZFAT Antibodies)-deficiency results in a loss of CD3zeta phosphorylation with dysregulation of ERK (show EPHB2 Antibodies) and Egr (show EGR1 Antibodies) activities leading to impaired positive selection.
The results of this study supported the model that the procognitive function of CD3zeta may be mediated through its involvement in the NMDAR (show GRIN1 Antibodies) downstream signaling pathway leading to CaMKII (show CAMK2G Antibodies)-dependent LTP (show SCP2 Antibodies) induction.
T cell CD3zeta deficiency enables multiorgan tissue inflammation.
Tyrosine phosphorylation of the TCR-zeta cytoplasmic domain regulates its association with the plasma membrane
The structure of the adaptor protein cd3zeta has been identified in the zebrafish genome.
The protein encoded by this gene is T-cell receptor zeta, which together with T-cell receptor alpha/beta and gamma/delta heterodimers, and with CD3-gamma, -delta and -epsilon, forms the T-cell receptor-CD3 complex. The zeta chain plays an important role in coupling antigen recognition to several intracellular signal-transduction pathways. Low expression of the antigen results in impaired immune response. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
CD247 antigen, zeta subunit
, CD3Z antigen, zeta polypeptide (TiT3 complex)
, CD3zeta chain
, T-cell antigen receptor complex, zeta subunit of CD3
, T-cell receptor T3 zeta chain
, T-cell surface glycoprotein CD3 zeta chain
, TCR zeta chain
, CD3 antigen, zeta polypeptide
, T-cell receptor T3 eta chain
, CD3 zeta
, CD247 molecule
, CD247 antigen
, T-cell receptor CD3 subunit zeta
, T-cell receptor CD3, subunit zeta
, CD3 zeta chain
, CD3 Zeta chain
, antigen CD3Z, zeta polypeptide
, T-cell receptor zeta chain