Anti-CBL antibody [YE323] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal CBL antibody. Carrier free. Suitable for ICC/IF, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
CBL2, RNF55, CBL, E3 ubiquitin-protein ligase CBL, Casitas B-lineage lymphoma proto-oncogene, Proto-oncogene c-Cbl, RING finger protein 55, RING-type E3 ubiquitin transferase CBL, Signal transduction protein CBL
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
This data was developed using ab32027, the same antibody clone in a different buffer formulation. Intracellular Flow Cytometry analysis of Jurkat (Human T cell leukemia T lymphocyte) cells labeling CBL with purified ab32027 at 1/30 dilution (10 μg/mL) (Red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
- WB
Unknown
Western blot - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
This data was developed using ab32027, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-CBL antibody [YE323] - C-terminal (<a href='/en-us/products/primary-antibodies/cbl-antibody-ye323-c-terminal-ab32027'>ab32027</a>) at 1/1000 dilution
Lane 1:
Raji (Human Burkitt's lymphoma B lymphocyte) whole cell lysate at 15 µg
Lane 2:
Rat testis lysate at 20 µg
Lane 3:
Rat thymus lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/2000 dilution
Predicted band size: 100 kDa
Observed band size: 110 kDa
false
- WB
Lab
Western blot - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
Lane 1 : Wild-type HAP1 whole cell lysate (20 μg)
Lane 2 : CBL knockout HAP1 whole cell lysate (20 μg)
Lane 3 : THP1 whole cell lysate (20 μg)
Lane 4 : Raji whole cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab32027 observed at 100 kDa. Red - loading control, ab9484, observed at 37 kDa.
Unpurified ab32027 was shown to specifically react with CBL in wild-type HAP1 cells as signal was lost in CBL knockout cells. Wild-type and CBL knockout samples were subjected to SDS-PAGE. ab32027 and ab9484 (Mouse anti-GAPDH loading control) were incubated overnight at 4°C at 1/5000 dilution and 1/20000 dilution respectively. Blots were developed 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 hour at room temperature before imaging.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab32027).
All lanes:
Western blot - Anti-CBL antibody [YE323] - C-terminal (<a href='/en-us/products/primary-antibodies/cbl-antibody-ye323-c-terminal-ab32027'>ab32027</a>)
Predicted band size: 100 kDa
false
- WB
Lab
Western blot - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
This data was developed using ab32027, the same antibody clone in a different buffer formulation.
Lanes 1-4 : Merged signal (red and green). Green - ab32027 observed at 110 kDa. Red - loading control ab8245 observed at 36 kDa.
ab32027 Anti-CBL antibody [YE323] - C-terminal was shown to specifically react with CBL in wild-type HEK293T cells. Loss of signal was observed when knockout cell line ab267245 (knockout cell lysate ab257200) was used. Wild-type and CBL knockout samples were subjected to SDS-PAGE. ab32027 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-CBL antibody [YE323] - C-terminal (<a href='/en-us/products/primary-antibodies/cbl-antibody-ye323-c-terminal-ab32027'>ab32027</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK293T cell lysate at 20 µg
Lane 2:
CBL knockout HEK293T cell lysate at 20 µg
Lane 2:
Western blot - Human CBL knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-cbl-knockout-hek-293t-cell-line-ab267245'>ab267245</a>)
Lane 3:
THP-1 cell lysate at 20 µg
Lane 4:
Raji cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/10000 dilution
Predicted band size: 100 kDa
Observed band size: 110 kDa
false
- WB
Lab
Western blot - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
This data was developed using the same antibody clone in a different buffer formulation (ab32027 ).
Western blot : Anti-CBL antibody [YE323] (ab32027) staining at 1/1000 dilution, shown in green; Mouse anti-CANX [CANX/1543] (ab238078) loading control staining at 1/20000 dilution, shown in magenta. In Western blot, ab32027 was shown to bind specifically to CBL. A band was observed at 105 kDa in wild-type HCT 116 cell lysates with no signal observed at this size in CBL knockout cell line. To generate this image, wild-type and CBL knockout HCT 116 cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.
All lanes:
Western blot - Anti-CBL antibody [YE323] - C-terminal (<a href='/en-us/products/primary-antibodies/cbl-antibody-ye323-c-terminal-ab32027'>ab32027</a>) at 1/1000 dilution
Lane 1:
Wild-type HCT 116 cell lysate at 20 µg
Lane 2:
CBL knockout HCT 116 cell lysate at 20 µg
Lane 2:
Western blot - Human CBL knockout HCT116 cell line (<a href='/en-us/products/cell-lines/human-cbl-knockout-hct116-cell-line-ab287255'>ab287255</a>)
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 105 kDa
false
- WB
Lab
Western blot - Anti-CBL antibody [YE323] - BSA and Azide free (AB236075)
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : 30 seconds
All lanes:
Western blot - Anti-CBL antibody [YE323] - C-terminal (<a href='/en-us/products/primary-antibodies/cbl-antibody-ye323-c-terminal-ab32027'>ab32027</a>) at 1/1000 dilution
Lane 1:
WEHI-231 (Mouse B cell lymphoma B lymphocyte) cell lysate at 10 µg
Lane 2:
F9 (Mouse embryonal carcinoma epithelial cell) cell lysate at 10 µg
Lane 3:
NIH/3T3 (Mouse embryonic fibroblast) cell lysate at 10 µg
Lane 4:
Mouse thymus lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 100 kDa
Observed band size: 110 kDa
false
Related conjugates and formulations (2)
-
Anti-CBL antibody [YE323] - C-terminal
-
578 PE
PE Anti-CBL antibody [YE323] - C-terminal
Reactivity data
Product details
ab236075 is the carrier-free version of ab32027.
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
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
The CBL protein acts as a negative regulator for several signaling pathways. It integrates into signaling complexes and modulates the activation of pathways by interacting with other proteins. CBL does not act alone; it commonly forms complexes with proteins such as Grb2 and p85 influencing downstream signaling influence in pathways. This regulation prevents excessive activation of signals that can lead to cellular proliferation or differentiation abnormally.
Pathways
CBL integrates into the ubiquitin-proteasome system and the Ras signaling pathway. Within these pathways CBL works to modulate cell surface receptors ensuring that signaling threshold is not surpassed. The importance of CBL in the Ras signaling pathway is highlighted by its interactions with proteins like Ras-GAP and SHP2. Through these interactions CBL controls the rate of signal transduction affecting cellular responses such as growth survival and motility.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
British journal of pharmacology 178:2246-2265 PubMed33085791
2021
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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