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anti-Human Cyclin E1 Antibodies:
anti-Mouse (Murine) Cyclin E1 Antibodies:
anti-Rat (Rattus) Cyclin E1 Antibodies:
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Human Monoclonal Cyclin E1 Primary Antibody for BI, FACS - ABIN967325
Darzynkiewicz, Gong, Juan, Ardelt, Traganos: Cytometry of cyclin proteins. in Cytometry 1997
Show all 11 Pubmed References
Human Monoclonal Cyclin E1 Primary Antibody for IP - ABIN2689485
Keyomarsi, Herliczek: The role of cyclin E in cell proliferation, development and cancer. in Progress in cell cycle research 1998
Show all 4 Pubmed References
Human Polyclonal Cyclin E1 Primary Antibody for IF (p), IHC (p) - ABIN1713477
Wang, Wang: Studying the relationship between cell cycle and Alzheimer's disease by gold nanoparticle probes. in Analytical biochemistry 2015
Human Monoclonal Cyclin E1 Primary Antibody for BI, FACS - ABIN967324
Faha, Harlow, Lees: The adenovirus E1A-associated kinase consists of cyclin E-p33cdk2 and cyclin A-p33cdk2. in Journal of virology 1993
Show all 10 Pubmed References
Mouse (Murine) Polyclonal Cyclin E1 Primary Antibody for FACS, IF (p) - ABIN670311
Xu, Zhang, Li, Li, Zhang: Concentration-Dependent Diversifcation Effects of Free Cholesterol Loading on Macrophage Viability and Polarization. in Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2015
Human Polyclonal Cyclin E1 Primary Antibody for ELISA, WB - ABIN560214
Hudelist, Singer, Pischinger, Kaserer, Manavi, Kubista, Czerwenka: Proteomic analysis in human breast cancer: identification of a characteristic protein expression profile of malignant breast epithelium. in Proteomics 2006
Human Polyclonal Cyclin E1 Primary Antibody for ICC, IF - ABIN4301619
Fu, Kohaar, Moore, Lenz, Figueroa, Tang, Porter-Gill, Chatterjee, Scott-Johnson, Garcia-Closas, Muchmore, Baris, Paquin, Ylaya, Schwenn, Apolo, Karagas, Tarway, Johnson, Mumy, Schned, Guedez, Jones et al.: The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease. ... in Cancer research 2014
Human Polyclonal Cyclin E1 Primary Antibody for ELISA - ABIN97973
Simone, Resta, Bagella, Giordano, Guanti: Cyclin E and chromosome instability in colorectal cancer cell lines. in Molecular pathology : MP 2002
Human Polyclonal Cyclin E1 Primary Antibody for IP, ELISA - ABIN2473143
Premack, Gardner: Role of ion channels in lymphocytes. in Journal of clinical immunology 1992
Show all 2 Pubmed References
The opposing effects of ORC1 (show ORC1L Antibodies) (represor) and CDC6 (show CDC6 Antibodies) (gene activator) in controlling the level of Cyclin E ensures genome stability and a mechanism for linking directly DNA replication and cell division commitment.
High cyclin E expression is associated with breast cancer.
High CCNC1 (show CNGA3 Antibodies) expression is associated with inflammatory breast cancer.
Inhibition of cell division cycle associated 2 (CDCA2 (show CDCA2 Antibodies)) suppressed the proliferation of lung adenocarcinoma (LAC (show LCT Antibodies)) cells via G1 phase arrest by downregulating cyclin E1(CCNE1), while overexpression of CDCA2 (show CDCA2 Antibodies) promoted LAC (show LCT Antibodies) cells proliferation by upregulating CCNE1.
a PI3K (show PIK3CA Antibodies)/PKCiota/cyclin E signaling pathway as a therapeutic target during ovarian tumorigenesis
Amplification of the G1-S regulatory genes, CCNE1, CCND1 and CdK6, represent an early event, which precedes ERBB2, EGFR, or KRAS amplification in gastric adenocarcinoma.
Amplification of 19q12 CCNE1/URI (show C19orf2 Antibodies) was found in 10.4% (28/270) and was significantly associated with type II endometrial cancer (EC) high grade, advanced FIGO stage, and aberrant tumor supressor p53 (show TP53 Antibodies) expression.
Data reveal that the presence of rs200996365, a SNP in high-linkage disequilibrium with rs8102137 residing in the center of a KLF5 (show KLF5 Antibodies) motif, alters KLF5 (show KLF5 Antibodies) binding to this genomic region and provide evidence that KLF5 (show KLF5 Antibodies) binds CCNE1 polymorphic intronic enhancer to confer increased bladder cancer risk.
Noxin (show C11orf82 Antibodies) facilitated the expression of Cyclin D1 (show CCND1 Antibodies) and Cyclin E1 through activating P38 (show CRK Antibodies)-activating transcription factor 2 (show ATF2 Antibodies) signaling pathway, thus enhanced cell growth of breast cancer
Results show that cyclin E1 and CDK2 (show CDK2 Antibodies) participate in STC1 (show STC1 Antibodies) promoting cell proliferation of prostate neoplasm cells.
These results demonstrate a repressor role for NFAT1 (show NFAT1 Antibodies) in cell cycle progression and Cyclin E expression in B lymphocytes, and suggest a potential function for NFAT1 (show NFAT1 Antibodies) protein in B cell malignancies.
This approach allowed us to determine the identity of cyclin E protein partners, as well as phosphorylation substrates of cyclins E (cyclin (show PCNA Antibodies) E1and cyclin E2 (show CCNE2 Antibodies))and its associated kinase, Cdk2 (show CDK2 Antibodies), in different mouse organs.
inhibition of PDK4 (show PDK4 Antibodies) activity in Hepatocellular carcinoma cells increased cyclin E1, cyclin A2 (show CCNA2 Antibodies), and E2F1 (show E2F1 Antibodies) proteins.
Spermatocytes lacking cyclin E2 (show CCNE2 Antibodies) and one E1 allele (E1+/-E2-/-) displayed a high rate of telomere abnormalities but can progress to pachytene and diplotene stages.
NF-kappaB (show NFKB1 Antibodies)-miR (show MLXIP Antibodies)-195/497-Igf1r (show IGF1R Antibodies)/Insr (show INSR Antibodies)-Ccnd2 (show CCND2 Antibodies)/Ccne1 plays important roles in myogenesis.
Myb (show MYB Antibodies) regulates Cyclin E1 expression in normal gastrointestinal tract epithelial cells and is required during intestinal tumorigenesis
These results highlight a new role for E-type cyclins (Ccne1 and Ccne2 (show CCNE2 Antibodies)) as important regulators of male meiosis.
Concurrent deletion of cyclin E1 and cyclin-dependent kinase 2 (show CDK2 Antibodies) in hepatocytes inhibits DNA replication and liver regeneration in mice.
Superoxide dismutase (show SOD1 Antibodies) induces G1-phase cell cycle arrest by down-regulated expression of Cdk-2 (show CDK2 Antibodies) and cyclin-E in sarcoma tumor cells.
Ablation of cyclin E led to a decreased number of synapses, reduced number and volume of dendritic spines, and resulted in impaired synaptic plasticity and memory formation.
miR (show MYLIP Antibodies)-15/16 and CPEB co-regulate cyclin E1 mRNA.
cyclin E is dynamically and highly conjugated to SUMO2 (show SUMO2 Antibodies)/3 on chromatin, independently of Cdk2 (show CDK2 Antibodies) activity and origin activation.
These results show that cyclin E destruction at the midblastula transition requires both phosphorylation and nuclear import, as well as proteasomal activity.
intestinal clock controls the expression of key cell cycle regulators, such as cdc2 (show CDK1 Antibodies), wee1 (show WEE1 Antibodies), p21 (show CDKN1A Antibodies), PCNA (show PCNA Antibodies) and cdk2 (show CDK2 Antibodies), but only weakly influences cyclin B1 (show CCNB1 Antibodies), cyclin B2 (show CCNB2 Antibodies) and cyclin E1 expression.
The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin forms a complex with and functions as a regulatory subunit of CDK2, whose activity is required for cell cycle G1/S transition. This protein accumulates at the G1-S phase boundary and is degraded as cells progress through S phase. Overexpression of this gene has been observed in many tumors, which results in chromosome instability, and thus may contribute to tumorigenesis. This protein was found to associate with, and be involved in, the phosphorylation of NPAT protein (nuclear protein mapped to the ATM locus), which participates in cell-cycle regulated histone gene expression and plays a critical role in promoting cell-cycle progression in the absence of pRB. Two alternatively spliced transcript variants of this gene, which encode distinct isoforms, have been described. Two additional splice variants were reported but detailed nucleotide sequence information is not yet available.
, G1/S-specific cyclin-E1
, G1/S-specific cyclin-E1-like
, g1/S-specific cyclin-E1-like
, cyclin Es
, cyclin Et
, cyclin E
, G1/S-specific cyclin-E2
, G1/S-specific cyclin-E3
, cyclin E3