×
For best experience we recommend to activate Javascript in your browser.
CEBPE antibody
CEBPE
Reactivity: Human, Rat, Mouse
IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-CEBPE Antibody
(hide)
Target
See all CEBPE Antibodies
CEBPE
(CCAAT/enhancer Binding Protein (C/EBP), epsilon (CEBPE))
Reactivity
Human, Rat, Mouse
Host
All hosts for CEBPE antibodies
Rabbit
Clonality
All clonalities for CEBPE antibodies
Polyclonal
Conjugate
All conjugates for CEBPE antibodies
This CEBPE antibody is un-conjugated
Application
All applications for CEBPE antibodies
Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human CEBPE (NP_001796.2).
Isotype
IgG
Top Product
Discover our top product CEBPE Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
(hide)
Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for CEBPE
(hide)
Target
CEBPE
(CCAAT/enhancer Binding Protein (C/EBP), epsilon (CEBPE))
Alternative Name
CEBPE (CEBPE Products )
Synonyms
CEBPE antibody, crp1 antibody, C/EBP-epsilon antibody, CRP1 antibody, C/EBPe antibody, Gm294 antibody, C/EPBe antibody, CCAAT/enhancer binding protein epsilon antibody, CCAAT/enhancer binding protein (C/EBP), epsilon antibody, CEBPE antibody, cebpe antibody, Cebpe antibody
Background
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.
Gene ID
1053
UniProt
Q15744
Pathways
Cellular Response to Molecule of Bacterial Origin
Recently viewed
(hide)