Loading...
|
ab86150 |
|
|
ab111659 |
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 >> Zinc Finger
Anti-Gli1 antibody
See all Gli1 products (3) ...
Rabbit polyclonal to Gli1
This antibody is specific for Gli1.
ICC/IF, WB, ELISAmore details
Reacts with
Human
Predicted to work with
Mouse, Cow, Dog
A region within Synthetic peptide: TNPSCGHPEV GRLGGGPALY PPPEGQVCNP LDSLDLDNTQ LDFVAILDEP , corresponding to amino acids 1007-1056 of Human Gli1
TNPSCGHPEV GRLGGGPALY PPPEGQVCNP LDSLDLDNTQ LDFVAILDEP
HepG2 cell lysate.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: None
Constituents: 2% Sucrose, PBS
Concentration information loading...
Protein A purified
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> Krueppel like factor
Cancer >> Oncoproteins/suppressors >> Tumor suppressors >> PTC & Wnt pathway
Stem Cells >> Signaling Pathways >> Hedgehog >> Nuclear
Neuroscience >> Neurology process >> Neural Signal Transduction
Epigenetics and Nuclear Signaling >> Transcription >> Domain Families >> Zinc Finger
Our Abpromise guarantee covers the use of ab49314 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: Use a concentration of 2.5 µg/mlDetects a band of approximately 118 kDa (predicted molecular weight: 118 kDa).Can be blocked with Gli1 peptide (1009-1058) (ab86150). (5% skim milk in PBS buffer. (An HRP conjugated anti-Rabbit IgG could be used as a secondary, a suggested dilution of 1/50000 to 1/100000). )
ELISA: 1/312500
Gli1 is a member of the Kruppel family of zinc finger proteins. The Gli transcription factors constitute the final effectors of the Hedgehog signalling pathway, which is critical to vertebrate development. Gli1 may play a role in craniofacial and digital development, as well as development of the central nervous system and gastrointestinal tract. Ectopic activation of Gli proteins is linked to tumorigenesis. In addition, both the Ras and Transforming Growth Factor Beta pathways also stimulate and/or induce Gli1 and Gli2 activity independently of Hedgehog ligands.
Cytoplasmic and Nuclear
Western blot - Gli1 antibody (ab49314)

Lane 1 : MARKER
Lane 2 : Anti-Gli1 antibody (ab49314) at 2.5 µg/ml
Lane 1 : As above
Lane 2 : HepG2 cell lysate at 10 µg
Secondary
Lane 1 :
Lane 2 : HRP conjugated anti-Rabbit IgG at 1/50000 dilution
Predicted band size : 118 kDa
Observed band size : 118 kDa
Western blot - Gli1 antibody (ab49314)

Lane 1 : Anti-Gli1 antibody (ab49314) at 1.25 µg/ml
Lane 2 : Anti-Gli1 antibody (ab49314) at 2.5 µg/ml
Lane 3 : Anti-Gli1 antibody (ab49314) at 5 µg/ml
Lane 1 : Cell lysate prepared from human HepG2 cells
Lane 2 : Cell lysate prepared from human HepG2 cells
Lane 3 : Cell lysate prepared from human HepG2 cells
Lysates/proteins at 25 µg per lane.
Predicted band size : 118 kDa
Immunocytochemistry/ Immunofluorescence-Gli1 antibody(ab49314)

ICC/IF image of ab49314 stained HepG2 cells. The cells were 4% formaldehyde fixed (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 (ab49314, 5µg/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.
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab49314? 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:

Lane 1 : MARKER
Lane 2 : Anti-Gli1 antibody (ab49314) at 2.5 µg/ml
Lane 1 : As above
Lane 2 : HepG2 cell lysate at 10 µg
Secondary
Lane 1 :
Lane 2 : HRP conjugated anti-Rabbit IgG at 1/50000 dilution
Predicted band size : 118 kDa
Observed band size : 118 kDa

Lane 1 : Anti-Gli1 antibody (ab49314) at 1.25 µg/ml
Lane 2 : Anti-Gli1 antibody (ab49314) at 2.5 µg/ml
Lane 3 : Anti-Gli1 antibody (ab49314) at 5 µg/ml
Lane 1 : Cell lysate prepared from human HepG2 cells
Lane 2 : Cell lysate prepared from human HepG2 cells
Lane 3 : Cell lysate prepared from human HepG2 cells
Lysates/proteins at 25 µg per lane.
Predicted band size : 118 kDa

ICC/IF image of ab49314 stained HepG2 cells. The cells were 4% formaldehyde fixed (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 (ab49314, 5µg/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.
2
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
