CBFB-Polyclonal Antibodies

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CBFB

Qty


Total
$220
Catalog #
A5305
Antibody Type
Polyclonal Antibody
Gene ID
865
Swiss Prot
Q13951
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC IF
Recommended DilutionWB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200
Calculated MW22kDa
Observed MWRefer to Figures
ImmunogenRecombinant protein of human CBFB
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
SynonymCBFB;CBF beta;PEBP2B;PEA2 beta;PEBP2 beta;
Images
  • A5305: image 1

    Western blot analysis of extracts of various cell lines, using CBFB antibody.

  • A5305: image 2

    Immunohistochemistry of paraffin-embedded human stomach cancer using CBFB antibody at dilution of 1:200 (x400 lens).

  • A5305: image 3

    Immunohistochemistry of paraffin-embedded Mouse brain using CBFB antibody at dilution of 1:100 (x400 lens).

  • A5305: image 4

    Immunofluorescence analysis of U2OS cell using CBFB antibody. Blue: DAPI for nuclear staining.

Background

The protein encoded by this gene is the beta subunit of a heterodimeric core-binding transcription factor belonging to the PEBP2/CBF transcription factor family which master-regulates a host of genes specific to hematopoiesis (e.g., RUNX1) and osteogenesis (e.g., RUNX2). The beta subunit is a non-DNA binding regulatory subunit; it allosterically enhances DNA binding by alpha subunit as the complex binds to the core site of various enhancers and promoters, including murine leukemia virus, polyomavirus enhancer, T-cell receptor enhancers and GM-CSF promoters. Alternative splicing generates two mRNA variants, each encoding a distinct carboxyl terminus. In some cases, a pericentric inversion of chromosome 16 [inv(16)(p13q22)] produces a chimeric transcript consisting of the N terminus of core-binding factor beta in a fusion with the C-terminal portion of the smooth muscle myosin heavy chain 11. This chromosomal rearrangement is associated with acute myeloid leukemia of the M4Eo subtype. Two transcript variants encoding different isoforms have been found for this gene.

Protocol

N/A

MSDS
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