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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> DNA / RNA >> Translation >> Regulation
Anti-EEF2 antibody [EP880Y] - C-terminal
See all EEF2 products (11) ...
Rabbit monoclonal [EP880Y] to EEF2 - C-terminal
WB, IP, Flow Cyt, IHC-P, ICC, ICC/IFmore details
Reacts with
Mouse, Rat, Human
A synthetic peptide corresponding to residues on the C terminal of human EEF2.
A431, NIH3T3, HeLa or 293 cell lysates. Human kidney carcinoma tissue.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.01% Sodium Azide
Constituents: 40% Glycerol, 0.05% BSA, Tissue culture supernatant, 0.15M Sodium chloride, 50mM Tris glycine, pH 7.4
Tissue culture supernatant
Monoclonal
EP880Y
IgG
Epigenetics and Nuclear Signaling >> DNA / RNA >> Translation >> Regulation
Western blot - EEF2 antibody [EP880Y] - Carboxyterminal end (ab75748)
(enlarge)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EEF2 antibody [EP880Y] - C-terminal (ab75748)
(enlarge)
Immunocytochemistry/ Immunofluorescence-EEF2 antibody [EP880Y] - C-terminal(ab75748)
(enlarge)
Our Abpromise guarantee covers the use of ab75748 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/10000 - 1/20000.Detects a band of approximately 95 kDa (predicted molecular weight: 95 kDa).
IP: 1/20
Flow Cyt: 1/20
IHC-P: 1/100 - 1/250.(Perform heat mediated antigen retrieval using 0.01M Sodium Citrate Buffer, pH 6.0 before commencing with IHC staining protocol.)
ICC: 1/100 - 1/250.
ICC/IF: Use a concentration of 1 µg/ml
Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome.
Belongs to the GTP-binding elongation factor family. EF-G/EF-2 subfamily.
Phosphorylation by EF-2 kinase completely inactivates EF-2.
Diphthamide is 2-[3-carboxyamido-3-(trimethyl-ammonio)propyl]histidine. Diphthamide can be ADP-ribosylated by diphtheria toxin and by Pseudomonas exotoxin A, thus arresting protein synthesis.
ISGylated.
Cytoplasm.
Target information above from: UniProt accessionP13639
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - EEF2 antibody [EP880Y] - Carboxyterminal end (ab75748)
![Western blot - EEF2 antibody [EP880Y] - Carboxyterminal end (ab75748)](/ps/datasheet/Images/75/ab75748/ab75748_1.jpg)
All lanes : Anti-EEF2 antibody [EP880Y] - C-terminal (ab75748) at 1/10000 dilution
Lane 1 : 293 cell lysate
Lane 2 : HeLa cell lysate
Lane 3 : A431 cell lysate
Lane 4 : NIH3T3 cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size : 95 kDa
Observed band size : 95 kDa
Additional bands at : 30 kDa,70 kDa. We are unsure as to the identity of these extra bands.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EEF2 antibody [EP880Y] - C-terminal (ab75748)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EEF2 antibody [EP880Y] - C-terminal (ab75748)](/ps/datasheet/Images/75/ab75748/ab75748_4.jpg)
ab75748 at 1/100 dilution staining EEF2 in human kidney carcinoma tissue.
Immunocytochemistry/ Immunofluorescence-EEF2 antibody [EP880Y] - C-terminal(ab75748)
![Immunocytochemistry/ Immunofluorescence-EEF2 antibody [EP880Y] - C-terminal(ab75748)](/ps/datasheet/images/75/ab75748/EEF2-Primary-antibodies-ab75748-1.jpg)
ICC/IF image of ab75748 stained HeLa 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 (ab75748, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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-EEF2 antibody [EP880Y] - C-terminal (ab75748)
![Flow Cytometry - Anti-EEF2 antibody [EP880Y] - C-terminal (ab75748)](/ps/datasheet/images/75/ab75748/EEF2-Primary-antibodies-ab75748-2.jpg)
Overlay histogram showing HeLa cells stained with ab75748 (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 (ab75748, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
ab75748 has not yet been referenced specifically in any publications.
Publishing research using ab75748? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
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![Western blot - EEF2 antibody [EP880Y] - Carboxyterminal end (ab75748)](/ps/datasheet/Images/75/ab75748/ab75748_1.jpg)
All lanes : Anti-EEF2 antibody [EP880Y] - C-terminal (ab75748) at 1/10000 dilution
Lane 1 : 293 cell lysate
Lane 2 : HeLa cell lysate
Lane 3 : A431 cell lysate
Lane 4 : NIH3T3 cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size : 95 kDa
Observed band size : 95 kDa
Additional bands at : 30 kDa,70 kDa. We are unsure as to the identity of these extra bands.
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - EEF2 antibody [EP880Y] - C-terminal (ab75748)](/ps/datasheet/Images/75/ab75748/ab75748_4.jpg)
ab75748 at 1/100 dilution staining EEF2 in human kidney carcinoma tissue.
![Immunocytochemistry/ Immunofluorescence-EEF2 antibody [EP880Y] - C-terminal(ab75748)](/ps/datasheet/images/75/ab75748/EEF2-Primary-antibodies-ab75748-1.jpg)
ICC/IF image of ab75748 stained HeLa 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 (ab75748, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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-EEF2 antibody [EP880Y] - C-terminal (ab75748)](/ps/datasheet/images/75/ab75748/EEF2-Primary-antibodies-ab75748-2.jpg)
Overlay histogram showing HeLa cells stained with ab75748 (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 (ab75748, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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