Anti-Mad2L1 antibody [EPR9853(B)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal Mad2L1 antibody. Carrier free. Suitable for WB and reacts with Human samples.
View Alternative Names
MAD2, MAD2L1, Mitotic spindle assembly checkpoint protein MAD2A, HsMAD2, Mitotic arrest deficient 2-like protein 1, MAD2-like protein 1
- WB
Unknown
Western blot - Anti-Mad2L1 antibody [EPR9853(B)] - BSA and Azide free (AB248948)
This data was developed using ab150371, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-Mad2L1 antibody [EPR9853(B)] (<a href='/en-us/products/primary-antibodies/mad2l1-antibody-epr9853b-ab150371'>ab150371</a>) at 1/10000 dilution
Lane 1:
293T cell lysates at 10 µg
Lane 2:
Jurkat cell lysates at 10 µg
Lane 3:
Raji cell lysates at 10 µg
Lane 4:
A431 cell lysates at 10 µg
Predicted band size: 24 kDa
false
- WB
Lab
Western blot - Anti-Mad2L1 antibody [EPR9853(B)] - BSA and Azide free (AB248948)
This data was developed using ab150371, the same antibody clone in a different buffer formulation.
Lanes 1 - 4 : Merged signal (red and green). Green - ab150371 observed at 24 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab150371 was shown to specifically react with in wild-type HAP1 cells as signal was lost in MAD2L1 knockout cells. Wild-type and MAD2L1 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% NF Milk. ab150371 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/10000 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.
All lanes:
Western blot - Anti-Mad2L1 antibody [EPR9853(B)] (<a href='/en-us/products/primary-antibodies/mad2l1-antibody-epr9853b-ab150371'>ab150371</a>) at 1/10000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
MAD2L1 knockout HAP1 whole cell lysate at 20 µg
Lane 3:
HeLa whole cell lysate at 20 µg
Lane 4:
A431 whole cell lysate at 20 µg
Predicted band size: 24 kDa
Observed band size: 24 kDa
false
Reactivity data
Product details
ab248948 is the carrier-free version of ab150371.
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
Mad2L1 serves as an essential component of the mitotic checkpoint complex. It forms a complex with other proteins such as Mad1 BubR1 and Cdc20 inhibiting the anaphase-promoting complex/cyclosome (APC/C). This interaction prevents the premature separation of sister chromatids by blocking the degradation of securin and cyclin B. These actions ensure that cells do not progress to anaphase until all chromosomes are correctly attached to the mitotic spindle.
Pathways
Mad2L1 interacts with proteins that regulate the spindle assembly checkpoint pathway and the cell cycle. It holds particular prominence within the mitotic spindle assembly checkpoint where it regulates progression from metaphase to anaphase through its interaction with proteins like Cdc20 and BubR1. Mad2L1 also plays a role in the DNA damage response cycle highlighting its importance in maintaining genomic stability.
Product protocols
- Visit the General 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