research use only

C/EBPβ Antibody [B2A6]

Cat.No.: F3008

    Application: Reactivity:

    Usage Information

    Dilution
    1:1000
    1:400 - 1:1600
    1:400 - 1:1600
    1:3200 - 1:6400
    Application
    WB, IHC, IF, FCM
    Reactivity
    Human, Monkey
    Source
    Rabbit Monoclonal Antibody
    Storage Buffer
    PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3
    Storage (from the date of receipt)
    -20°C (avoid freeze-thaw cycles), 2 years
    Predicted MW
    46 (LAP), 48 (Full Length)

    Datasheet & SDS

    Biological Description

    Specificity
    C/EBPβ Antibody [B2A6] detects endogenous levels of total C/EBPβ protein.
    Clone
    B2A6
    Synonym(s)
    CEBPB; CCAAT/enhancer-binding protein beta; C/EBP beta; Liver activator protein (LAP); Liver-enriched inhibitory protein (LIP); Nuclear factor NF-IL6; Transcription factor 5 (TCF-5); TCF5; PP9092
    Background
    C/EBPβ is a basic leucine-zipper (bZIP) transcription factor fundamental for the acute-phase response, adipogenesis, hematopoiesis, and immune regulation, functioning as homo- or heterodimers through its C-terminal leucine zipper that binds palindromic DNA consensus sequences via an N-terminal basic region, with three isoforms, LAP1, LAP2 (full-length activators), and LIP (truncated repressor), arising from alternative translation. It activates target genes such as IL-6, IL-8, and SAA by direct promoter binding and cooperative recruitment with NF-κB and STAT3 during inflammatory responses, promotes adipocyte differentiation by inducing PPARγ and C/EBPα, and regulates granulopoiesis through G-CSF and M-CSF expression. Phosphorylation at specific motifs, such as Thr235 by MAPK/p38, facilitates nuclear translocation and dimerization, while GSK3β-mediated Ser276 phosphorylation modulates its activation state in response to LPS and cytokines. C/EBPβ amplification can drive acute myeloid leukemia by disrupting PU.1 function, whereas deficiency impairs liver regeneration and macrophage polarization; overexpression of the LIP isoform is associated with poor prognosis in breast cancer due to its effects on cell cycle progression.
    References
    • https://pubmed.ncbi.nlm.nih.gov/12006103/
    • https://pubmed.ncbi.nlm.nih.gov/19351437/

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