Anti-MALT1/MLT antibody [EPR24445-129] - BSA and Azide free
- KO Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal MALT1/MLT antibody. Carrier free. Suitable for IP, WB and reacts with Human, Mouse samples.
View Alternative Names
MLT, MALT1, Mucosa-associated lymphoid tissue lymphoma translocation protein 1, MALT lymphoma-associated translocation, Paracaspase
- IP
Supplier Data
Immunoprecipitation - Anti-MALT1/MLT antibody [EPR24445-129] - BSA and Azide free (AB283590)
This data was developed using ab283573, the same antibody clone in a different buffer formulation.
MALT1/MLT was immunoprecipitated from 0.35 mg Ramos (human Burkitt's lymphoma B lymphocyte), whole cell lysate 10 ug with ab283573 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab283573 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Ramos (human Burkitt's lymphoma B lymphocyte), whole cell lysate 10 ug
Lane 2 : ab283573 IP in Ramos whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab283573 in Ramos whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 minutes
All lanes:
Immunoprecipitation - Anti-MALT1/MLT antibody [EPR24445-129] (<a href='/en-us/products/primary-antibodies/malt1-mlt-antibody-epr24445-129-ab283573'>ab283573</a>)
Predicted band size: 92 kDa
Observed band size: 92 kDa
false
- WB
Lab
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] - BSA and Azide free (AB283590)
This data was developed using ab283573, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
ab283573 Anti-MALT1/MLT antibody [EPR24445-129] was shown to specifically react with MALT1/MLT in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab264930 (knockout cell lysate ab257149) was used. Wild-type and MALT1/MLT knockout samples were subjected to SDS-PAGE.
Exposure time : 37 seconds
All lanes:
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] (<a href='/en-us/products/primary-antibodies/malt1-mlt-antibody-epr24445-129-ab283573'>ab283573</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
MALT1/MLT knockout Hela whole cell lysate at 20 µg
Lane 3:
Ramos (human Burkitt's 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 1/20000 dilution
Predicted band size: 92 kDa
Observed band size: 92 kDa
false
- WB
Lab
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] - BSA and Azide free (AB283590)
This data was developed using ab283573, the same antibody clone in a different buffer formulation.
Western blot : Rabbit Monoclonal[EPR24445-129] to MALT1/MLT ab283573 staining at 1/1000 dilution, shown in green; Mouse anti GAPDH (ab8245) loading control staining at 1/20,000 dilution, shown in magenta. A band was observed at kDa in Wild-type HCT 116 ab288559 cell lysates with no signal observed at this size in MALT1 knockout HCT 116 ab286597 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 & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] (<a href='/en-us/products/primary-antibodies/malt1-mlt-antibody-epr24445-129-ab283573'>ab283573</a>) at 1/1000 dilution
Lane 1:
Wild-type HCT 116 ab288559 at 20 µg
Lane 2:
Western blot - Human MALT1 knockout HCT116 cell line (<a href='/en-us/products/cell-lines/human-malt1-knockout-hct116-cell-line-ab286597'>ab286597</a>) at 20 µg
Lane 3:
HeLa at 20 µg
Lane 4:
Ramos at 20 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 92 kDa
Observed band size: 95 kDa
false
- WB
Lab
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] - BSA and Azide free (AB283590)
This data was developed using ab283573, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Exposure time : Lane 1 : 26 seconds ; Lane 2 : 70 seconds
All lanes:
Western blot - Anti-MALT1/MLT antibody [EPR24445-129] (<a href='/en-us/products/primary-antibodies/malt1-mlt-antibody-epr24445-129-ab283573'>ab283573</a>) at 1/1000 dilution
Lane 1:
Mouse thymus tissue lysate at 20 µg
Lane 2:
A20 (mouse reticum sarcoma B lymphocyte) whole cell lysate at 20 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 1/20000 dilution
Predicted band size: 92 kDa
Observed band size: 92 kDa
false
Related conjugates and formulations (1)
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Anti-MALT1/MLT antibody [EPR24445-129]
Reactivity data
Product details
ab283590 is the carrier-free version of ab283573.
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
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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