Product Name
C/EBP-epsilon (CEBPE), Polyclonal Antibody
Full Product Name
C/EBP-epsilon Antibody
Product Synonym Names
C/EBP epsilon; CCAAT/enhancer binding protein epsilon; CEBPE
Product Gene Name
anti-CEBPE antibody
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Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q15744
Specificity
C/EBP-epsilon Antibody detects endogenous levels of total C/EBP-epsilon protein.
Purity/Purification
Purified from rabbit antiserum by affinity-chromatography using immunogen.
Form/Format
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Concentration
1 mg/ml (lot specific)
Target Modification
Unmodified/Total
Immunogen
The antiserum was produced against synthesized peptide derived from human C/EBP-epsilon.
Preparation and Storage
Stable at -20 degree C for at least 1 year.
Other Notes
Small volumes of anti-CEBPE antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Applications Tested/Suitable for anti-CEBPE antibody
Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), ELISA (EIA)
Application Notes for anti-CEBPE antibody
WB: 1:500~1:1000
IHC: 1:50~1:100
IF: 1:100~1:500
ELISA: 1:1000
Immunofluorescence (IF) of anti-CEBPE antibody
Immunofluorescence analysis of HeLa cells, using C/EBP-epsilon Antibody. The picture on the right is blocked with the synthesized peptide.

Immunohistochemistry (IHC) of anti-CEBPE antibody
Immunohistochemistry analysis of paraffin-embedded human brain tissue, using C/EBP-epsilon Antibody. The picture on the right is blocked with the synthesized peptide.

Western Blot (WB) of anti-CEBPE antibody
Western blot analysis of lysates from JurKat cells, treated with Insulin 0.01U/ml 15', using C/EBP-epsilon Antibody. The lane on the right is blocked with the synthesized peptide.

NCBI/Uniprot data below describe general gene information for CEBPE. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001796.2
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NCBI GenBank Nucleotide #
NM_001805.3
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UniProt Primary Accession #
Q15744
[Other Products]
UniProt Secondary Accession #
Q15745; Q8IYI2; Q99803[Other Products]
UniProt Related Accession #
Q15744[Other Products]
NCBI Official Full Name
CCAAT/enhancer-binding protein epsilon
NCBI Official Synonym Full Names
CCAAT/enhancer binding protein epsilon
NCBI Official Symbol
CEBPE??[Similar Products]
NCBI Official Synonym Symbols
CRP1; C/EBP-epsilon
??[Similar Products]
NCBI Protein Information
CCAAT/enhancer-binding protein epsilon
UniProt Protein Name
CCAAT/enhancer-binding protein epsilon
Protein Family
CCAAT/enhancer-binding protein
UniProt Gene Name
CEBPE??[Similar Products]
UniProt Synonym Gene Names
C/EBP epsilon??[Similar Products]
NCBI Summary for CEBPE
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. [provided by RefSeq, Jul 2008]
UniProt Comments for CEBPE
Transcriptional activator (PubMed:26019275). C/EBP are DNA-binding proteins that recognize two different motifs: the CCAAT homology common to many promoters and the enhanced core homology common to many enhancers. Required for the promyelocyte-myelocyte transition in myeloid differentiation (PubMed:10359588).
Research Articles on CEBPE
1. Data show that both CEBPE and SMARCD2 loss-of-function mutations identified in patients with neutrophil-specific granule deficiency (SGD) abolish the interaction with SWI/SNF and secondary granule gene expression, thus providing a molecular basis for this disease.
Precautions
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Disclaimer
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