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Anti-ATF6 antibody [70B1413] - ChIP Grade
See all ATF6 products (8) ...
Mouse monoclonal [70B1413] to ATF6 - ChIP Grade
This antibody recognizes both full length and active/Cleaved ATF6.
ICC/IF, IHC-P, IHC-Fr, IP, ChIP, Flow Cyt, WBmore details
Reacts with
Mouse, Rat, Rabbit, Hamster, Human
Full length protein (Human).
293 whole cell extract.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: 0.05% BSA, PBS
Concentration information loading...
Protein G purified
Monoclonal
70B1413
IgG1
Our Abpromise guarantee covers the use of ab11909 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use at an assay dependent dilution.
IHC-P: Use at an assay dependent dilution.
IHC-Fr: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
ChIP: Use at an assay dependent dilution.
Flow Cyt: Use 1µg for 106 cells.
WB: Use a concentration of 1 - 5 µg/ml.Detects a band of approximately 90 kDa (predicted molecular weight: 75 kDa).
Transcription factor that acts during endoplasmic reticulum stress by activating unfolded protein response target genes. Binds DNA on the 5'-CCAC[GA]-3'half of the ER stress response element (ERSE) (5'-CCAAT-N(9)-CCAC[GA]-3') and of ERSE II (5'-ATTGG-N-CCACG-3'). Binding to ERSE requires binding of NF-Y to ERSE. Could also be involved in activation of transcription by the serum response factor.
Ubiquitous.
Belongs to the bZIP family. ATF subfamily.
Contains 1 bZIP domain.
The basic domain functions as a nuclear localization signal.
The basic leucine-zipper domain is sufficient for association with the NF-Y trimer and binding to ERSE.
During unfolded protein response an approximative 50 kDa fragment containing the cytoplasmic transcription factor domain is released by proteolysis. The cleavage seems to be performed sequentially by site-1 and site-2 proteases.
N-glycosylated. The glycosylation status may serve as a sensor for ER homeostasis, resulting in ATF6 activation to trigger the unfolded protein response (UPR).
Phosphorylated in vitro by MAPK14/P38MAPK.
Endoplasmic reticulum membrane and Nucleus. Under ER stress the cleaved N-terminal cytoplasmic domain translocates into the nucleus.
Target information above from: UniProt accessionP18850
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
- ATF6 antibody [70B1413] - ChIP Grade (ab11909)
![- ATF6 antibody [70B1413] - ChIP Grade (ab11909)](/ps/datasheet/Images/11/ab11909/11909_2.jpg)
Ab11909 (3ug/ml) staining of mouse ATF6 in NIH3T3 cell lysate by Western Blot. The ~36 kDa observed band has not been characterized; it may be an ATF6 breakdown/cleavage product.
Immunocytochemistry/ Immunofluorescence-ATF6 antibody [70B1413] - ChIP Grade(ab11909)
![Immunocytochemistry/ Immunofluorescence-ATF6 antibody [70B1413] - ChIP Grade(ab11909)](/ps/datasheet/images/11/ab11909/ATF6-Primary-antibodies-ab11909-1.jpg)
ICC/IF image of ab11909 stained MCF7 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab11909, 10µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Flow Cytometry-Anti-ATF6 antibody [70B1413] - ChIP Grade(ab11909)
![Flow Cytometry-Anti-ATF6 antibody [70B1413] - ChIP Grade(ab11909)](/ps/datasheet/images/11/ab11909/ATF6-Primary-antibodies-ab11909-2.jpg)
Overlay histogram showing HeLa cells stained with ab11909 (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. The cells were then incubated with the antibody (ab11909, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells ) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See 1 publication for this product
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![- ATF6 antibody [70B1413] - ChIP Grade (ab11909)](/ps/datasheet/Images/11/ab11909/11909_2.jpg)
Ab11909 (3ug/ml) staining of mouse ATF6 in NIH3T3 cell lysate by Western Blot. The ~36 kDa observed band has not been characterized; it may be an ATF6 breakdown/cleavage product.
![Immunocytochemistry/ Immunofluorescence-ATF6 antibody [70B1413] - ChIP Grade(ab11909)](/ps/datasheet/images/11/ab11909/ATF6-Primary-antibodies-ab11909-1.jpg)
ICC/IF image of ab11909 stained MCF7 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab11909, 10µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
![Flow Cytometry-Anti-ATF6 antibody [70B1413] - ChIP Grade(ab11909)](/ps/datasheet/images/11/ab11909/ATF6-Primary-antibodies-ab11909-2.jpg)
Overlay histogram showing HeLa cells stained with ab11909 (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. The cells were then incubated with the antibody (ab11909, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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