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CEBPE expression was highest in multipotent progenitor cells (S1) and declined sharply as cells progressed to B (zeige TDO2 Antikörper)-cell-committed progenitors, including pre-B-I cells (S2), pre-B-II cells (S3) and immature B cells (S4)
IKZF1 (zeige IKZF1 Antikörper) rs10235796 C allele, IKZF1 (zeige IKZF1 Antikörper) rs6964969A>G, CDKN2A rs3731246 G>C, and CDKN2A rs3731246 C allele were signi fi cantly associated with Acute Lymphoblastic Leukemia in Yemenis of Arab-Asian descent. Borderline association found in IKZF1 (zeige IKZF1 Antikörper) rs4132601 T>G variant. No associations found with IKZF1 (zeige IKZF1 Antikörper) rs11978267 or rs7789635, DDC (zeige DDC Antikörper) rs3779084; rs880028; rs7809758, CDKN2A rs3731217, CEBPE rs2239633; rs12434881
Data show that both CEBPE and SMARCD2 (zeige SMARCD2 Antikörper) loss-of-function mutations identified in patients with neutrophil-specific granule deficiency (SGD (zeige SGCD Antikörper)) abolish the interaction with SWI (zeige SMARCA1 Antikörper)/SNF (zeige SNRPA Antikörper) and secondary granule gene expression, thus providing a molecular basis for this disease.
PML (zeige PML Antikörper)/RARalpha (zeige RARA Antikörper) synergizes with C/EBPepsilon to reactivate the C/EBPepsilon target G0S2 (zeige G0S2 Antikörper), thereby contributing to All-trans retinoic acid -mediated acute promyelocytic leukemia (zeige PML Antikörper) differentiation and potentially, clinical remission.
the rs7088318 (PIP4K2A (zeige PIP4K2A Antikörper)) and rs2239633 (CEBPE) polymorphisms were not associated with ALL risk.
The minor allele of the CEBPE variant associated with lower basophil count has been previously associated with Amerindian ancestry and higher risk of acute lymphoblastic leukemia in Hispanics.
variants within IKZF1 (zeige IKZF1 Antikörper), ARID5B (zeige ARID5B Antikörper), and CEBPE were associated with pediatric ALL risks.
Genotypic and allelic frequencies differed significantly between cases and controls at IKZF1 (zeige IKZF1 Antikörper)-rs4132601 (p=0.039, p=0.015) and ARID5B (zeige ARID5B Antikörper)-rs10821936 (p=0.028, p=0.026).
variants within IKZF1 (zeige IKZF1 Antikörper), ARID5B (zeige ARID5B Antikörper), and CEBPE were associated with increased acute lymphoblastic leukemia (ALL) risk, and the effects for ARID5B (zeige ARID5B Antikörper) and CEBPE were most prominent in high-hyperdiploid ALL subtype in the California Hispanic population
Data indicate no significant associations of transcription factors rs4132601 (IKZF1 (zeige IKZF1 Antikörper)), rs7089424 (ARID5B (zeige ARID5B Antikörper)) and rs2239633 (CEBPE) with risk of pediatric non-Hodgkin lymphoma (NHL (zeige RTEL1 Antikörper)).
study suggests that the myeloid specific factor C/EBPepsilon is involved in systemic lipid metabolism and that silencing of C/EBPepsilon could decrease the development of atherosclerosis.
in the absence of CCAAT enhancer binding protein epsilon (C/EBPepsilon), there is not only incomplete differentiation of granulocytes, but myelopoiesis is disrupted and neutrophils have abnormal chemotaxis
C/EBP epsilon gene as an important transcription factor required for normal function and development of macrophages.
C/EBPepsilon interacts with Rb and E2F1 (zeige E2F1 Antikörper) during granulocytic differentiation
in the later stages of myeloid development, MMP8 (zeige MMP8 Antikörper) and other SGP genes are coordinately upregulated, and members of the C/EBP (zeige CEBPA Antikörper) family, in particular C/EBPalpha (zeige CEBPA Antikörper) and C/EBPepsilon, play specific and unique roles in upregulating their expression
Gfi-1 down-regulates C/EBPepsilon expression; increased expression of C/EBPepsilon as a consequence of loss of Gfi-1 function may be deleterious to the proliferation and survival of early myeloid cells
the N terminus of C/EBPepsilon is solely responsible for most aspects of myeloid differentiation, and these events are differentially affected by c-Myc (zeige MYC Antikörper)
the requirement for C/EBP epsilon in mediating BPI (zeige BPI Antikörper) gene expression in myeloid cells in vitro and in vivo.
The type IV isoform of PML (zeige PML Antikörper) interacted with PU.1, promoted its association with p300 (zeige NOTCH1 Antikörper), and then enhanced PU.1-induced transcription and granulocytic differentiation and PU.1 directly activates the transcription of the C/EBPepsilon gene.
Phosphorylation of PML (zeige PML Antikörper) was required for stimulating C/EBP epsilon-dependent transcription and accelerating C/EBP epsilon-induced granulocytic differentiation.
The protein encoded by this gene is a bZIP transcription factor which can bind as a homodimer to certain DNA regulatory regions. It can also form heterodimers with the related protein CEBP-delta. The encoded protein may be essential for terminal differentiation and functional maturation of committed granulocyte progenitor cells. Mutations in this gene have been associated with Specific Granule Deficiency, a rare congenital disorder. Multiple variants of this gene have been described, but the full-length nature of only one has been determined.
CCAAT/enhancer binding protein (C/EBP), epsilon
, CCAAT/enhancer-binding protein epsilon
, CCAAT/enhancer binding protein epsilon
, c/EBP epsilon
, C/EBP-related protein 1
, CCAAT/enhancer binding protein , epsilon
, c/EBP-related protein 1