Brachyury / Bry Recombinant Rabbit Monoclonal Antibody [JE44-11]
cat.: ET7109-35
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P, FC, IP
Clonality: Monoclonal
Clone number: JE44-11
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclean 950.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 47 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human Brachyury aa 236-435 / 435.
Positive control: Mouse embryo notochord tissue, A549.
Subcellular location: Nucleus.
Recommended Dilutions:
  WB
  IHC-P
  FC
  IP

1:500-1:1,000
1:1,000
1:50-1:100
Use at an assay dependent concentration.
Uniprot #: SwissProt: O15178 Human | P20293 Mouse
Alternative names: BRAC_HUMAN Brachyury homolog Brachyury protein Bry MGC104817 Protein T SAVA T T brachyury homolog T brachyury transcription factor T Protein T, brachyury homolog (mouse) TFT Transcription factor T
Images
ET7109-35_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded mouse embryo notochord tissue with Rabbit anti-Brachyury / Bry antibody (ET7109-35) at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET7109-35) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ET7109-35_2.jpg Fig2: Flow cytometric analysis of Brachyury / Bry was done on A549 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET7109-35, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.