Product nameAnti-BTF antibody - C-terminal
See all BTF primary antibodies
DescriptionRabbit polyclonal to BTF - C-terminal
Tested applicationsSuitable for: WB, ICC/IFmore details
Species reactivityReacts with: Human
Predicted to work with: Mouse, Rat, Cow, Pig
Recombinant fragment within Human BTF (C terminal). The exact sequence is proprietary.
Database link: Q9NYF8
- WB: HEK-293T, A431, HeLa and HepG2 whole cell extracts. ICC/IF: A431 cells.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Storage bufferpH: 7.00
Preservative: 0.025% Proclin
Constituents: PBS, 1% BSA, 20% Glycerol
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab226796 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/500 - 1/3000. Predicted molecular weight: 106 kDa.|
|ICC/IF||1/100 - 1/1000.|
FunctionDeath-promoting transcriptional repressor.
Cellular localizationCytoplasm. Nucleus.
- Information by UniProt
- Bcl 2 associated transcription factor antibody
- Bcl-2-associated transcription factor 1 antibody
- BCL2 associated transcription factor 1 antibody
All lanes : Anti-BTF antibody - C-terminal (ab226796) at 1/1000 dilution
Lane 1 : HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell extract
Lane 2 : A431 (human epidermoid carcinoma cell line) whole cell extract
Lane 3 : HeLa (human epithelial cell line from cervix adenocarcinoma) whole cell extract
Lane 4 : HepG2 (human liver hepatocellular carcinoma cell line) whole cell extract
Lysates/proteins at 30 µg per lane.
Predicted band size: 106 kDa
4% paraformaldehyde-fixed, A431 (human epidermoid carcinoma cell line) cells stained for BTF (green) using ab226796 at 1/500 dilution in ICC/IF.
The cytoskeleton is stained with phalloidin (red).
ab226796 has not yet been referenced specifically in any publications.