Loading...
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> HLH / Leucine Zipper >> Leucine Zipper
Anti-JunB antibody
See all JunB products (9) ...
Rabbit polyclonal to JunB
Antibody detects endogenous levels of JunB protein around Serine 259.
ICC/IF, WB, IP, IHC-P, ELISAmore details
Reacts with
Mouse, Rat, Human
Synthetic non-phosphopeptide derived from Human JunB around the phosphorylation site of Serine 259.
Extracts of Hela cells and breast carcinoma tissue.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS (without Mg2+ and Ca2+), 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Our Abpromise guarantee covers the use of ab31421 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 a concentration of 5 µg/ml
WB: 1/500 - 1/1000.Predicted molecular weight: 35 kDa.
IP: Use at an assay dependent dilution.
IHC-P: 1/50 - 1/100.
ELISA: 1/20000
The cJun proto-oncogene was first identified as the cellular homolog of the avian sarcoma virus vjun oncogene. JunB and JunD have been shown to be almost identical to cJun in their C terminal regions, which are involved in dimerization and DNA binding, whereas their N terminal domains, which are involved in transcriptional activation, diverge. JunB is a transcription factor involved in regulating gene activity following the primary growth factor response. It binds to the DNA sequence 5'-TGA[CG]TCA-3'.
Nuclear
Immunohistochemistry (Paraffin-embedded sections) - JunB antibody (ab31421)

ab31421 at a 1:50-1:100 dilution, staining JunB in human breast carcinoma using Immunohistochemistry, Paraffin Embedded Tissue.
Left image : Un-treated.
Right image : Antibody pre-incubated with synthesized peptide.
Western blot - JunB antibody (ab31421)

All lanes : Anti-JunB antibody (ab31421) at 1/500 dilution
Lane 1 : Extracts of Hela cells.
Lane 2 : Extracts of Hela cells. Antibody pre-incubated with synthesized peptide.
Predicted band size : 35 kDa
Observed band size : 41 kDa (why is the actual band size different from the predicted?)
Immunocytochemistry/ Immunofluorescence-Anti-JunB antibody(ab31421)

ICC/IF image of ab31421 stained Hek293 cells. The cells were 4% formaldehyde (10 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 (ab31421, 5µg/ml) overnight at +4°C. The secondary antibody (green) was 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.
This product has been referenced in:
See all 3 publications for this product
Publishing research using ab31421? 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.
Find concentration of your lot:

ab31421 at a 1:50-1:100 dilution, staining JunB in human breast carcinoma using Immunohistochemistry, Paraffin Embedded Tissue.
Left image : Un-treated.
Right image : Antibody pre-incubated with synthesized peptide.

All lanes : Anti-JunB antibody (ab31421) at 1/500 dilution
Lane 1 : Extracts of Hela cells.
Lane 2 : Extracts of Hela cells. Antibody pre-incubated with synthesized peptide.
Predicted band size : 35 kDa
Observed band size : 41 kDa (why is the actual band size different from the predicted?)

ICC/IF image of ab31421 stained Hek293 cells. The cells were 4% formaldehyde (10 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 (ab31421, 5µg/ml) overnight at +4°C. The secondary antibody (green) was 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.
0
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
