Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal UNC5B antibody. Carrier free. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat, Transfected cell lysate - Mouse samples.
View Alternative Names
Unc5h2, Unc5b, Netrin receptor UNC5B, Protein unc-5 homolog 2, Protein unc-5 homolog B
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using ab313565, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized Neuro-2a (mouse neuroblastoma neuroblast) cells labelling UNC5B with ab313565 at 1/50 (10.56 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing membranous staining in Neuro-2a cells.Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using ab313565, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Neuro-2a (mouse neuroblastoma neuroblast) cells labelling UNC5B with ab313565 at 1/50 dilution (1 ug)/Red (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, ab150081) at 1/5000 dilution was used as the secondary antibody.
- WB
Supplier Data
Western blot - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using ab313565, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : Daudi, Raji(PMID : 12655055), HL-60 (PMID : 12655055, PMID : 25171009).
In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution.
All lanes:
Western blot - Anti-UNC5B antibody [EPR26173-186] (<a href='/en-us/products/primary-antibodies/unc5b-antibody-epr26173-186-ab313565'>ab313565</a>) at 1/1000 dilution
Lane 1:
Human brain tissue lysate at 20 µg
Lane 2:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Daudi (human Burkitts lymphoma lymphoblast) whole cell lysate at 20 µg
Lane 4:
HL-60 (human Acute Promyelocytic Leukemia promyeloblast) whole cell lysate at 20 µg
Lane 5:
Raji (human Burkitts lymphoma B lymphocyte) whole cell 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 1/100000 dilution
Observed band size: 50 kDa,65 kDa,130 kDa
false
Exposure time: 26s
- WB
Lab
Western blot - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab313565).
Western blot : Anti-UNC5B antibody [EPR26173-186] ab313565 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH ab8245 loading control staining at 1/20000 dilution, shown in magenta. A band was observed at 120, 50 kDa in Wild-type U-87 MG cell lysates with a truncated product observed at 100 kDa in CRISPR-Cas9 Edited cell line. To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc 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 800CW and Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-UNC5B antibody [EPR26173-186] (<a href='/en-us/products/primary-antibodies/unc5b-antibody-epr26173-186-ab313565'>ab313565</a>) at 1/1000 dilution
Lane 1:
Wild-type U-87 MG (UNBOILED) whole cell lysate at 20 µg
Lane 2:
UNC5B knockout U-87 MG (UNBOILED) whole cell lysate at 20 µg
Lane 3:
SH-SY5Y (UNBOILED) whole cell lysate at 20 µg
Lane 4:
U-2 OS (UNBOILED) whole cell lysate at 20 µg
Lane 5:
Daudi (UNBOILED) whole cell lysate at 20 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 104 kDa
Observed band size: 120 kDa,50 kDa
false
- WB
Supplier Data
Western blot - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using ab313565, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds
All lanes:
Western blot - Anti-UNC5B antibody [EPR26173-186] (<a href='/en-us/products/primary-antibodies/unc5b-antibody-epr26173-186-ab313565'>ab313565</a>) at 1/1000 dilution
Lane 1:
Mouse spinal cord tissue lysate at 20 µg
Lane 2:
Mouse brain tissue lysate at 20 µg
Lane 3:
bEnd.3 (mouse brain endothelial cell) while cell lysate at 20 µg
Lane 4:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 5:
Rat brain tissue lysate at 20 µg
Lane 6:
C6 (rat glial tumor glial cell) whole cell 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 1/100000 dilution
Observed band size: 50 kDa,65 kDa,130 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-UNC5B antibody [EPR26173-186] - BSA and Azide free (AB313566)
This data was developed using ab313565, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST This antibody has no cross reaction with mouse UNC5A, UNC5C and UNC5D. In Western blot, anti-His antibody (ab213204) staining at 1/5000 dilution. Exposure time : 3 seconds
All lanes:
Western blot - Anti-UNC5B antibody [EPR26173-186] (<a href='/en-us/products/primary-antibodies/unc5b-antibody-epr26173-186-ab313565'>ab313565</a>) at 1/1000 dilution
Lane 1:
293T transfected with a mouse UNC5A expression vector containi a His tag whole cell lysate at 40 µg
Lane 2:
293T transfected with a mouse UNC5B vector containi a His tag whole cell lysate at 2 µg
Lane 3:
293T transfected with a mouse UNC5C vector containi a His tag whole cell lysate at 10 µg
Lane 4:
293T transfected with a mouse UNC5D vector containi a His tag whole cell 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 1/100000 dilution
Observed band size: 130 kDa
false
Exposure time: 3s
Related conjugates and formulations (1)
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Anti-UNC5B antibody [EPR26173-186]
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.
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 conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Scientists understand UNC5B to mediate the anti-angiogenic effects within tissues. It is an essential component of the signaling pathways that govern apoptosis in response to cellular conditions. UNC5B forms part of a larger receptor complex with Netrin-1 which influences cellular directionality and guidance by affecting cytoskeletal dynamics.
Pathways
The UNC5B receptor prominently participates in the Netrin signaling pathway. Within this pathway UNC5B interacts with other proteins such as DCC (deleted in colorectal cancer) that are involved in axonal guidance and neuronal navigation. It also plays a part in the apoptotic signaling pathways which are important for regulating cell survival and programmed cell death.
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