Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Knockout Tested Rabbit Recombinant Monoclonal NF2 / Merlin antibody. Carrier free. Suitable for WB and reacts with Human, Mouse samples.
View Alternative Names
SCH, NF2, Merlin, Moesin-ezrin-radixin-like protein, Neurofibromin-2, Schwannomerlin, Schwannomin
- WB
Unknown
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free (AB247805)
This data was developed using ab109244, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] (<a href='/en-us/products/primary-antibodies/nf2-merlin-antibody-epr25732-ab109244'>ab109244</a>) at 1/50000 dilution
Lane 1:
HeLa cell lysate at 10 µg
Lane 2:
MCF7 cell lysate at 10 µg
Lane 3:
Jurkat cell lysate at 10 µg
Lane 4:
PC3 cell lysate at 10 µg
Predicted band size: 70 kDa
false
- WB
Lab
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free (AB247805)
False colour image of Western blot : Anti-NF2 / Merlin antibody [EPR2573(2)] staining at 1/50000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab109244 was shown to bind specifically to NF2 / Merlin. A band was observed at 74 kDa in wild-type HepG2 cell lysates with no signal observed at this size in NF2 knockout cell line ab277859 (knockout cell lysate ab283826). To generate this image, wild-type and NF2 knockout HepG2 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 (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) at 1/20000 dilution.
All lanes:
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] (<a href='/en-us/products/primary-antibodies/nf2-merlin-antibody-epr25732-ab109244'>ab109244</a>) at 1/50000 dilution
Lane 1:
Wild-type HepG2 cell lysate at 20 µg
Lane 2:
NF2 knockout HepG2 cell lysate at 20 µg
Lane 2:
Western blot - Human NF2 (Merlin) knockout Hep G2 cell line (<a href='/en-us/products/cell-lines/human-nf2-merlin-knockout-hep-g2-cell-line-ab277859'>ab277859</a>)
Predicted band size: 70 kDa
Observed band size: 74 kDa
false
- WB
Lab
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free (AB247805)
This data was developed using ab109244, the same antibody clone in a different buffer formulation.
Lane 1 : Wild type HAP1 whole cell lysate (20 μg)
Lane 2 : NF2 knockout HAP1 whole cell lysate (20 μg)
Lanes 1 - 2 : Merged signal (red and green). Green - ab109244 observed at 70 kDa. Red - loading control, ab18058, observed at 130 kDa.
ab109244 was shown to specifically react with NF2 in wild type cells as signal was lost in NF2 knockout cells. Wild-type and NF2 knockout samples were subjected to SDS-PAGE. ab109244 and ab18058 (Mouse anti Vinculin loading control) were incubated overnight at 4°C at 50000 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-NF2 / Merlin antibody [EPR2573(2)] (<a href='/en-us/products/primary-antibodies/nf2-merlin-antibody-epr25732-ab109244'>ab109244</a>)
Predicted band size: 70 kDa
false
- WB
Lab
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free (AB247805)
This data was developed using the same antibody clone in a different buffer formulation (ab109244).
Lanes 1 - 2 : Merged signal (red and green). Green - ab109244 observed at 60 kDa. Red - loading control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37kDa.
ab109244 was shown to react with NF2 in wild-type HeLa cells in western blot with loss of signal observed in NF2 knockout cell line ab261796 (NF2 knockout cell lysate ab257179). Wild-type and NF2 knockout HeLa cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3% milk in TBS-T (0.1% Tween®) before incubation with ab109244 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4°C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated 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 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] (<a href='/en-us/products/primary-antibodies/nf2-merlin-antibody-epr25732-ab109244'>ab109244</a>) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
NF2 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human NF2 (Merlin) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-nf2-merlin-knockout-hela-cell-line-ab261796'>ab261796</a>)
Predicted band size: 70 kDa
Observed band size: 60 kDa
false
- WB
Supplier Data
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] - BSA and Azide free (AB247805)
False colour image of Western blot : Anti-NF2 / Merlin antibody [EPR2573(2)] staining at 1/50000 dilution, shown in green; Mouse anti-GAPDH antibody [6C5] (ab8245) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab109244 was shown to bind specifically to NF2 / Merlin. A band was observed at 73 kDa in wild-type A549 cell lysates with no signal observed at this size in NF2 knockout cell line. To generate this image, wild-type and NF2 knockout A549 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 (ab109244).
All lanes:
Western blot - Anti-NF2 / Merlin antibody [EPR2573(2)] (<a href='/en-us/products/primary-antibodies/nf2-merlin-antibody-epr25732-ab109244'>ab109244</a>) at 1/50000 dilution
Lane 1:
Wild-type A549 cell lysate at 20 µg
Lane 2:
NF2 knockout A549 cell lysate at 20 µg
Lane 3:
SH-SY5Y cell lysate at 20 µg
Predicted band size: 70 kDa
Observed band size: 73 kDa
false
Related conjugates and formulations (1)
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Anti-NF2 / Merlin antibody [EPR2573(2)]
Reactivity data
Product details
ab247805 is the carrier-free version of ab109244.
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
The NF2 protein functions to control cell proliferation differentiation and motility. It associates with the cytoskeleton acting as a bridge between cell surface proteins and the actin cytoskeleton. Merlin as part of the ERM (ezrin radixin moesin) family contributes to the assembly of protein complexes at the cell membrane. Through its interactions it plays a significant role in maintaining proper cell signaling and structural integrity.
Pathways
NF2 protein integrates into the Hippo signaling pathway which regulates organ size by controlling cell growth and apoptosis. Within this pathway Merlin interacts with members such as YAP1 and LATS1/2 moderating their activity to prevent over-proliferation of cells. NF2 also connects with the mTOR pathway which is critical for cell metabolism and growth further emphasizing its regulatory functions in cellular homeostasis.
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