Anti-CCNE1 antibody produced in rabbit

IgG fraction of antiserum, buffered aqueous solution


biological source


Quality Level

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies




buffered aqueous solution

species reactivity



proximity ligation assay: suitable
western blot: 1 μg/mL



UniProt accession no.

shipped in

dry ice

storage temp.


Gene Information

human ... CCNE1(898)

General description

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. (provided by RefSeq)
Cyclin E1 (CCNE1) is encoded by the gene mapped to human chromosome 19q12–q21.


CCNE1 (NP_001229.1, 1 a.a. ~ 410 a.a) full-length human protein.


Biochem/physiol Actions

Elevated expression of Cyclin E1 (CCNE1) results in ovarian cancer. Thus, CCNE1 can be considered as a potential therapeutic target in ovarian cancer. CCNE1 might act as a key functional mediator in G1/S transition and is considered to be a one of new direct target genes of microRNA (miRNA) precursor mir-7 in human hepatocellular carcinoma (HCC).

Physical form

Solution in phosphate buffered saline, pH 7.4


Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.


12 - Non Combustible Liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

MicroRNA-7 arrests cell cycle in G1 phase by directly targeting CCNE1 in human hepatocellular carcinoma cells.
Zhang X
Biochemical and Biophysical Research Communications, 443, 1078-1084 (2014)
Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinoma.
Snijders AM
Oncogene, 22, 4281-4286 (2003)
Gene amplification CCNE1 is related to poor survival and potential therapeutic target in ovarian cancer.
Nakayama N
Cancer, 116, 2621-2634 (2010)
Varsha Meghnani et al.
Biochimica et biophysica acta, 1842(7), 1017-1027 (2014-03-13)
The formation of melanoma metastases from primary tumor cells is a complex phenomenon that involves the regulation of multiple genes. We have previously shown that the receptor for advanced glycation end products (RAGE) was up-regulated in late metastatic stages of...
Ka Tat Siu et al.
Molecular and cellular biology, 34(17), 3244-3258 (2014-06-25)
The Fbw7 ubiquitin ligase critically regulates hematopoietic stem cell (HSC) function, though the precise contribution of individual substrate ubiquitination pathways to HSC homeostasis is unknown. In the work reported here, we used a mouse model in which we introduced two...

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