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Anti-BID Antibody Y8
|A synthetic peptide corresponding to residues before the BH3 domain of human Bid was used as the immunogen. This antibody does not cross-react with other Bcl-2 family members.|
||0.5~1.0 mg/ml (Lot Dependent)
|WB, IHC, FC
||WB: 1:1000; IHC-P: Use at an assay dependent dilution; ICC/IF: 1:100; FC: 1:50; IP: 1:10
|PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%|
|Does not react with Mouse, Rat
|Homo sapiens BH3 interacting domain death agonist (BID), transcript variant 1|
|Bid, BH3 interacting domain death agonist, is a pro-apoptotic member of the Bcl-2 family of proteins that regulate aptosis. Bid is localized to the cytosol in an inactive precursor form. Upon caspase-8 binding in the Fas signaling pathway, Bid is cleaved and the active Bid fragment translocates to mitochondria and induces cytochrome c release and the resulting apoptotic cascade (1-3). Bid contains a BH3 domain which allows it to dimerize with and counter the death repressor effects of Bcl-2. BID has also been shown to heterodimerize with Bcl-x and the death agonist Bax (4).|
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Western blot - Bid antibody [Y8]; Anti-Bid antibody [Y8] at 1/1000 dilution + Jurkat cell lysate.Predicted band size : 22 kDa.Observed band size : 22 kDa.
Western blot - Bid antibody [Y8]; All lanes : Anti-Bid antibody [Y8] at 1/500 dilution.Lane 1 : Whole cell lysate prepared from breast cancer clinical extract.Lane 2 : Whole cell lysate prepared from breast cancer clinical extract.Lane 3 : Whole cell lysate prepared from MCF7 cells.Lysates/proteins at 20 µg per lane.Secondary.Goat anti-rabbit IgG-HRP at 1/1000 dilution.developed using the ECL technique.Predicted band size : 22 kDa.Observed band size : 22 kDa.Exposure time : 25 minutesImage courtesy of an anonymous Abreview.
Immunohistochemistry (Paraffin-embedded sections) - Bid antibody [Y8]; Immunohistochemical analysis of paraffin-embedded human prostate carcinoma using ab32060 at 1/100 dilution.
Flow Cytometry-Anti-Bid antibody [Y8](ab32060); Overlay histogram showing HeLa cells stained with ab32060 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody for 30 min at 22°C. The secondary antibody used was DyLight? 488 goat anti-rabbit IgG (H+L) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1µg/1x10^6 cells) used under the same conditions. Unlabelled sample (blue line). Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.