Anti-ABL1 antibody [EPR23406-32]
- 20ul selling size
- KO Validated
- RabMAb
- Recombinant
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Knockout Tested Rabbit Recombinant Monoclonal ABL1 antibody. Suitable for WB, Flow Cyt (Intra) and reacts with Human samples.
View Alternative Names
ABL, JTK7, ABL1, Tyrosine-protein kinase ABL1, Abelson murine leukemia viral oncogene homolog 1, Abelson tyrosine-protein kinase 1, Proto-oncogene c-Abl, p150
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-ABL1 antibody [EPR23406-32] (AB254341)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed, 90% methanol-permeabilized K-562 (Human chronic myelogenous leukemia lymphoblast) cells labelling ABL1 with ab254341 at 1/500 dilution (0.1μg) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
- WB
Lab
Western blot - Anti-ABL1 antibody [EPR23406-32] (AB254341)
Lanes 1 - 3 : Merged signal (red and green). Green - ab254341 observed at 130 kDa. Red - loading control, ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55 kDa. ab254341 was shown to react with ABL1 in wild-type HeLa cells in western blot. The bands observed in ABL1 knockout cell line ab265612 (ABL1 knockout cell lysate ab263077) below 130 kDa may represent truncated forms and cleaved fragments. This has not been investigated further. HeLa wild-type and ABL1 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1 % Tween®) before incubation with ab254341 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4°C at a 1 : 1000 dilution and a 1 : 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 : 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-ABL1 antibody [EPR23406-32] (ab254341) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human ABL1 knockout HeLa cell lysate (<a href='/en-us/products/cell-lysates/human-abl1-knockout-hela-cell-lysate-ab263077'>ab263077</a>) at 20 µg
Lane 3:
K562 cell lysate at 20 µg
Predicted band size: 122 kDa
Observed band size: 130 kDa
false
- WB
Lab
Western blot - Anti-ABL1 antibody [EPR23406-32] (AB254341)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Fresh lysates are recommended for loading to minimize target degradation.
Exposure time : 48 seconds.
All lanes:
Western blot - Anti-ABL1 antibody [EPR23406-32] (ab254341) at 1/1000 dilution
Lane 1:
MCF7 (human breast adenocarcinoma epithelial cell) whole cell lysate at 10 µg
Lane 2:
Daudi (human burkitts lymphoma lymphoblast) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 122 kDa
Observed band size: 135 kDa
false
- WB
Lab
Western blot - Anti-ABL1 antibody [EPR23406-32] (AB254341)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure time : 48 seconds.
All lanes:
Western blot - Anti-ABL1 antibody [EPR23406-32] (ab254341) at 1/1000 dilution
All lanes:
K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 122 kDa
Observed band size: 135 kDa,210 kDa
false
- WB
Lab
Western blot - Anti-ABL1 antibody [EPR23406-32] (AB254341)
Lanes 1 - 3 : Merged signal (red and green). Green - ab254341 observed at 130 kDa. Red - loading control, ab7291 (Mouse anti-Alpha Tubulin [DM1A]) observed at 55 kDa.
ab254341 was shown to react with ABL1 in wild-type HeLa cells in western blot. The bands observed in ABL1 knockout cell line ab265612 (ABL1 knockout cell lysate ab263077) below 130 kDa may represent truncated forms and cleaved fragments. This has not been investigated further. HeLa wild-type and ABL1 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1 % Tween®) before incubation with ab254341 and ab7291 (Mouse anti-Alpha Tubulin [DM1A]) overnight at 4°C at a 1 : 1000 dilution and a 1 : 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 : 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-ABL1 antibody [EPR23406-32] (ab254341) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
ABL1 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human ABL1 knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-abl1-knockout-hela-cell-line-ab265612'>ab265612</a>)
Lane 3:
K562 cell lysate at 20 µg
Predicted band size: 122 kDa
Observed band size: 130 kDa
false
Related conjugates and formulations (1)
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Anti-ABL1 antibody [EPR23406-32] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ABL1 functions by regulating key processes like cell cycle progression actin dynamics and cell adhesion. ABL1 participates as part of larger protein complexes that modulate cellular movement and gene transcription. When activated it phosphorylates a range of substrates that leads to various cellular outcomes. ABL1 operates in the cytoplasm and nucleus influencing both cytoskeletal rearrangement and DNA repair which highlights its critical function in maintaining cellular integrity and response to damage.
Pathways
ABL1 interacts in both the mitogenic and apoptotic pathways including involvement in the MAPK and PI3K/AKT pathways. ABL1 interfaces with proteins like CRK and GRB2 in these pathways integrating signals that determine cell fate decisions. Through its kinase activity ABL1 mediates signaling cascades that impact cellular growth and survival responding dynamically to internal and external cues.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com