Anti-BACE1 antibody [EPR3956] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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(1 Publication)
Knockout Tested Rabbit Recombinant Monoclonal BACE1 antibody. Carrier free. Suitable for IP, WB and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
BACE, KIAA1149, BACE1, Beta-secretase 1, Aspartyl protease 2, Beta-site amyloid precursor protein cleaving enzyme 1, Memapsin-2, Membrane-associated aspartic protease 2, ASP2, Asp 2, Beta-site APP cleaving enzyme 1
- IP
Lab
Immunoprecipitation - Anti-BACE1 antibody [EPR3956] - BSA and Azide free (AB237595)
ab108394 (purified) at 1/40 immunoprecipitating BACE1 in human fetal brain whole tissue lysate.
Lane 1 (input) : human fetal brain whole tissue lysate (10µg)
Lane 2 (+) : ab108394 + human fetal brain whole tissue lysate (10µg).
Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab108394 in human fetal brain whole tissue lysate.
For western blotting, ab131366 VeriBlot for IP (HRP) was used as the secondary antibody (1/1500).
Blocking buffer and concentration : 5% NFDM/TBST.
Diluting buffer and concentration : 5% NFDM /TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab108394).
All lanes:
Immunoprecipitation - Anti-BACE1 antibody [EPR3956] (<a href='/en-us/products/primary-antibodies/bace1-antibody-epr3956-ab108394'>ab108394</a>)
Predicted band size: 39 kDa,56 kDa
Observed band size: 42 kDa,70 kDa
false
- WB
Lab
Western blot - Anti-BACE1 antibody [EPR3956] - BSA and Azide free (AB237595)
Lane 1 : Wild type HAP1 whole cell lysate (20 μg)
Lane 2 : BACE1 knockout HAP1 whole cell lysate (20 μg)
Lane 3 : SH-SY5Y whole cell lysate (20 μg)
Lane 4 : Human brain whole cell lysate (20 μg)
Lanes 1 - 4 : Merged signal (red and green). Green - ab108394 observed at 70 kDa. Red - loading control, ab9484, observed at 37 kDa.
ab108394 was shown to recognize BACE1 in wild type cells as signal was lost at the expected MW in BACE1 knockout cells. Additional cross-reactive bands were observed in the wild-type and knockout cells. Wild-type and BACE1 knockout samples were subjected to SDS-PAGE. ab108394 and ab9484 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1000 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 (ab108394).
All lanes:
Western blot - Anti-BACE1 antibody [EPR3956] (<a href='/en-us/products/primary-antibodies/bace1-antibody-epr3956-ab108394'>ab108394</a>)
Predicted band size: 56 kDa
false
- WB
Lab
Western blot - Anti-BACE1 antibody [EPR3956] - BSA and Azide free (AB237595)
False colour image of Western blot : Anti-BACE1 antibody [EPR3956] staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab108394 was shown to bind specifically to BACE1. A band was observed at 60/70 kDa in wild-type SH-SY5Y cell lysates with no signal observed at this size in Bace1 knockout cell line ab280078 (knockout cell lysate ab280137). To generate this image, wild-type and Bace1 knockout SH-SY5Y 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. This data was developed using the same antibody clone in a different buffer formulation (ab108394)
Lanes 1 - 3:
Western blot - Anti-BACE1 antibody [EPR3956] (<a href='/en-us/products/primary-antibodies/bace1-antibody-epr3956-ab108394'>ab108394</a>) at 1/1000 dilution
Lanes 1 - 3:
Western blot - Anti-BACE1 antibody [EPR3956] - BSA and Azide free (ab237595) at 1/1000 dilution
Lane 1:
Wild-type SH-SY5Y cell lysate at 20 µg
Lane 2:
Bace1 knockout SH-SY5Y cell lysate at 20 µg
Lane 2:
Western blot - Human BACE1 knockout SH-SY5Y cell line (<a href='/en-us/products/unavailable/human-bace1-knockout-sh-sy5y-cell-line-ab280078'>ab280078</a>)
Lane 2:
Western blot - Human BACE1 knockout SH-SY5Y cell lysate (ab280137)
Lane 3:
HAP1 cell lysate at 20 µg
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680R at 1/20000 dilution
Observed band size: 70 kDa,60 kDa
false
- WB
Lab
Western blot - Anti-BACE1 antibody [EPR3956] - BSA and Azide free (AB237595)
This data was developed using ab108394, the same antibody clone in a different buffer formulation.
Western blot : Anti-BACE1 antibody [EPR3956] (ab108394) staining at 1/1000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in magenta. In Western blot, ab108394 was shown to bind specifically to BACE1. A band was observed at 56 kDa in wild-type U-87 MG cell lysates with no signal observed at this size in BACE1 knockout cell line. To generate this image, wild-type and BACE1 knockout U-87 MG cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % 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-BACE1 antibody [EPR3956] (<a href='/en-us/products/primary-antibodies/bace1-antibody-epr3956-ab108394'>ab108394</a>) at 1/1000 dilution
Lane 1:
Wild-type U-87 MG cell lysate at 20 µg
Lane 2:
Western blot - Human BACE1 knockout U-87 MG cell line (ab306623)
Lane 2:
BACE1 knockout U-87 MG cell lysate at 20 µg
Lane 3:
Wild-type SH-SY5Y cell lysate at 20 µg
Lane 4:
BACE1 knockout SH-SY5Y <a href='/en-us/products/unavailable/human-bace1-knockout-sh-sy5y-cell-line-ab280078'>ab280078</a> cell lysate at 20 µg
Secondary
Lanes 1 - 4:
Goat anti-Rabbit IgG H&L 800CW at 1/20000 dilution
Lanes 1 - 4:
Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 56 kDa
false
Related conjugates and formulations (1)
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Anti-BACE1 antibody [EPR3956]
Reactivity data
Product details
ab237595 is the carrier-free version of ab108394.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
BACE1 initiates the amyloidogenic pathway of APP processing which involves amyloid-beta generation. BACE1 doesn't function alone but acts as part of a complex that aids in protein substrate recognition and processing. Its activity contributes to physiological processes like myelination and axonal guidance indicating its importance beyond amyloid production.
Pathways
BACE1 is integral to the amyloidogenic pathway which is important in Alzheimer's disease development. It interacts with proteins such as presenilin 1 a part of the gamma-secretase complex that further processes the amyloid-beta precursor. Furthermore BACE1 links to synaptic functions and neural signaling pathways highlighting its multifaceted roles.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Frontiers in behavioral neuroscience 17:1172091 PubMed37273278
2023
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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