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Human CD4 Protein expressed in HEK-293 Cells - ABIN2180791
Crise, Buonocore, Rose: CD4 is retained in the endoplasmic reticulum by the human immunodeficiency virus type 1 glycoprotein precursor. in Journal of virology 1990
Show all 3 references for ABIN2180791
Mouse (Murine) CD4 Protein expressed in Human Cells - ABIN2007381
Ryu, Truneh, Sweet, Hendrickson: Structures of an HIV and MHC binding fragment from human CD4 as refined in two crystal lattices. in Structure (London, England : 1993) 1994
Show all 2 references for ABIN2007381
Rhesus Monkey CD4 Protein expressed in HEK-293 Cells - ABIN2180786
Rudd, Trevillyan, Dasgupta, Wong, Schlossman: Pillars article: the CD4 receptor is complexed in detergent lysates to a protein-tyrosine kinase (pp58) from human T lymphocytes. 1988. in Journal of immunology (Baltimore, Md. : 1950) 2010
TCF-1-deficient CD4+ CD8+ double positive thymocytes fail to undergo TCR alpha Valpha14-Jalpha18 rearrangement and produce significantly fewer Natural killer T cells.
High-fat diet - induced type 2 diabetes decreases the number of ileum IL17 (show IL17A Proteins)/RORgammaT CD4 T cells.
Results indicate that hypomethylation of Cd4 antigen correlates with stable CD4 expression.
CD4 is expressed in distinct nanoclusters and does not colocalize with T-cell receptor and active protein tyrosine kinase (show YES1 Proteins) p56lck (show LCK Proteins)
This study establishes an important role of IgE in abdominal aortic aneurysms pathogenesis by activating CD4+ T cells, mast cells, and macrophages.
5-kb cis (show CISH Proteins)-element is required in postselection thymocytes for helper lineage commitment, presumably mediating the maintenance of CD4 expression, and suggest that inactivation of the cis (show CISH Proteins)-element by DNA methylation (show HELLS Proteins)
Both type I CD8 (show CD8A Proteins)+ cytotoxic (Tc1 (show C8orf4 Proteins)) cells and interleukin (IL)-17 (show IL17A Proteins)-producing CD8 (show CD8A Proteins)+ (Tc17) cells mediate effective antitumor immunity through distinct effector mechanisms, but Tc1 (show C8orf4 Proteins) cells are superior to Tc17 cells in mediating tumor regression.
Accumulation of CD4 positive effector T cells is a critical step in the progression from mild glomerulonephritis to severe crescentic glomerulonephritis accompanied by tubulointerstitial inflammation and loss of kidney function.
Thymic selection does not appear to play an important role in CD4+CD8+ T cell receptor (TCR)beta repertoire overlap between individuals.
CD4-positive cell deficiency impairs IFN-gamma (show IFNG Proteins) production by CD8 (show CD8A Proteins)-positive effector cells at the site of Mycobacterium tuberculosis infection in mice.
The percentage of lamina propia CD4+LAP+ cells is increased in active ulcerative colitis, showing reduced suppressor activity due to their increased proportion of intracellular IL-17 (show IL17A Proteins) expression.
The study gives insights into the role of CD4 on cell membrane mechanical characteristics.
A decrease of CD4(+) CD25 (show IL2RA Proteins)(+) CD127 (show IL7R Proteins)(low) FoxP3 (show FOXP3 Proteins)(+) regulatory T cells with impaired suppressive function had been found in untreated ulcerative colitis patients.
Redox shuffling of the allosteric disulfide results in previously undescribed conformational changes in CD4 that are likely important for its interaction with its protein partners.
Increased levels of activated and highly susceptible HIV-1 target cells, reduced CD4 and enhanced CXCR4 (show CXCR4 Proteins) cell surface expression, together with the high susceptibility to FAS (show FAS Proteins)-induced programmed cell death may contribute to the rapid CD4+ T cell depletion.
HRB (show HRB Proteins) knock-down affected CD4 downregulation induced by Nef but not by HIV-1 Vpu.
Increased CD4, IL-17 (show IL17A Proteins), and COX-2 expression are associated with subclinical inflammation in malar melasma.
Sustained expression of CD83 (show CD83 Proteins) was observed when CD4+ T cells were induced by transforming growth factor-beta to differentiate into CD4+CD25 (show IL2RA Proteins)+ forkhead box P3 (show FOXP3 Proteins)+ regulatory T (iTreg) cells.
CHD in Chinese population is strongly associated with HLA-DRB1*01 and DRB1*04 haplotypes, and formation of CD4(+)CD28(null) T cells was related to HLA-DRB1*01, DRB1*04, and DRB1*15 alleles.
These results lead to a model for the docking of the full AP-2 (show GTF3A Proteins) tetramer to membranes as bound to Nef, such that the cytosolic tail of CD4 is situated to interact with its binding site on Nef.
The frequency and expression of a CD4 variant in microminipigs are described.
These data help clarify the regulatory mechanism of DNA methylation (show HELLS Proteins) of the CD4 gene in non-immune cell response to virus replication.
These results suggested that the SNPs in CD4 and STAT5b (show STAT5B Proteins) may be potential genetic markers for SCS (show TWIST1 Proteins) and milk/protein (show CSN2 Proteins) yields selecting and warrant further functional research.
The DNA methylation (show HELLS Proteins) level of the CD4 gene was strongly influenced by mastitis in Chinese Holstein cattle.
These findings revealed that despite the existence of a distinct bovine CD4(+)CD25 (show IL2RA Proteins)(high) T cell population, which showed Foxp3 (show FOXP3 Proteins) transcription/expression, natural regulatory activity did not reside in this cell population
The absence of CD4 T cells results in failure to produce antibodies that neutralize CD4-independent SIV Envs and CD4-pretriggered control SIV Envs.
study found noticeable variation in the first variable region V1 of CD4 and in intron six among the subspecies of chimpanzees.
This gene encodes a membrane glycoprotein of T lymphocytes that interacts with major histocompatibility complex class II antigenes and is also a receptor for the human immunodeficiency virus. This gene is expressed not only in T lymphocytes, but also in B cells, macrophages, and granulocytes. It is also expressed in specific regions of the brain. The protein functions to initiate or augment the early phase of T-cell activation, and may function as an important mediator of indirect neuronal damage in infectious and immune-mediated diseases of the central nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been identified in this gene.
, T-cell surface glycoprotein CD4
, T-cell differentiation antigen L3T4
, T-cell surface antigen T4/Leu-3
, T-cell surface glycoprotein CD4 precursor (T-cell surface antigen T4/Leu-3) (T-cell differentiation antigen L3T4)
, CD4 antigen (p55)
, CD4 receptor
, W3/25 antigen
, lymphocyte antigen CD4
, cell surface glycoprotein CD4