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Western blot analysis of CEBPE using rabbit polyclonal CEBPE Antibody using 293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected (Lane 2) with the CEBPE gene.
Western blot analysis in NCI-H460 cell line lysates (35ug/lane).
Western blot analysis in mouse heart tissue lysates (35ug/lane).
Western blot analysis of CEBPE using rabbit polyclonal CEBPE Antibody using 293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected (Lane 2) with the CEBPE gene.

CEBPE Antibody

CATALOG NUMBER: 57-485

Clonality:
Polyclonal
Tested Applications:
WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Immunogen:
This CEBPE antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 203-232 amino acids from the C-terminal region of human CEBPE.
Conjugate:
Unconjugated
Tested Applications:
WB
Application Note:
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
31 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
CEBPE
Additional Names:
CCAAT/enhancer-binding protein epsilon, C/EBP epsilon, CEBPE
Protein Accession Number:
Q15744
Protein Gi Number:
62512175
Ncbi Gene Id Number:
1053
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
The protein encoded by this gene is a bZIP transcriptionfactor which can bind as a homodimer to certain DNA regulatoryregions. It can also form heterodimers with the related proteinCEBP-delta. The encoded protein may be essential for terminaldifferentiation and functional maturation of committed granulocyteprogenitor cells. Mutations in this gene have been associated withSpecific Granule Deficiency, a rare congenital disorder. Multiplevariants of this gene have been described, but the full-lengthnature of only one has been determined.
Background Reference 1:
Prasad, R.B., et al. Blood (2009) In press :
Background Reference 2:
Papaemmanuil, E., et al. Nat. Genet. 41(9):1006-1010(2009)
Background Reference 3:
Bedi, R., et al. Blood 113(2):317-327(2009)
Background Reference 4:
Cloutier, A., et al. J. Immunol. 182(1):563-571(2009)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

57-485

List Size:
400 ul

List Price:

$469.00

Out of stock

Datasheet
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