Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal MAG/GMA antibody. Carrier free. Suitable for ICC/IF, IP, WB, IHC-Fr, IHC-P and reacts with Rat, Human, Mouse samples. Cited in 1 publication.
View Alternative Names
GMA, MAG, Myelin-associated glycoprotein, Siglec-4a
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human sciatic nerve tissue labeling MAG/GMA with ab277524 at 1/5000 dilution (0.1008 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on human sciatic nerve. The section was incubated with ab277524 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling MAG/GMA with ab277524 at 1/5000 dilution (0.1008 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on human cerebrum.The section was incubated with ab277524 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse hippocampus tissue labeling MAG/GMA with ab277524 at 1/2000 dilution (0.252 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on mouse hippocampus. (PMID : 25523827)The section was incubated with ab277524 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat cerebellum tissue labeling MAG/GMA with ab277524 at 1/500 dilution (1.008 ug/ml) followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat cerebellum is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized rat primary neural/glia cell cells labelling MAG/GMA with ab277524 at 1/50 dilution (10.08 ug/ml), followed by ab150080 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in rat primary oligodendroglia cells. Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection. Anti-Myelin Basic Protein rat monoclonal antibody was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab277241 at 1/50 dilution, followed by ab150157 at 1/1000 dilution.
-ve control 2 : Anti-Myelin Basic Protein rat monoclonal antibody, followed by ab150080 at 1/1000 dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse liver tissue labeling MAG/GMA with ab277524 at 1/100 dilution (5.04 ug/ml) followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Negative control : No staining on mouse liver (PMID2432614) is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat liver tissue labeling MAG/GMA with ab277524 at 1/100 dilution (5.04 ug/ml) followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Negative control : No staining on rat liver (PMID2432614) is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat hippocampus tissue labeling MAG/GMA with ab277524 at 1/2000 (0.252 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on rat hippocampus. (PMID : 17705198, 27000654 )The section was incubated with ab277524 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse cerebellum tissue labeling MAG/GMA with ab277524 at 1/500 dilution (1.008 ug/ml) followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse cerebellum is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- WB
Lab
Western blot - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
MAG is a glycoprotein. The molecular weight observed is consistent with what has been described in the literature (PMID : 1716323).
Negative control : Liver (PMID : 2432614).
Exposure time : 26 seconds.
All lanes:
Western blot - Anti-MAG/GMA antibody [EPR24276-125] (<a href='/en-us/products/primary-antibodies/mag-gma-antibody-epr24276-125-ab277524'>ab277524</a>) at 1/1000 dilution
Lane 1:
Human cerebellum tissue lysate at 20 µg
Lane 2:
Human liver tissue lysate at 20 µg
Secondary
All lanes:
VeriBlot for IP secondary antibody(HRP)(<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/1000 dilution
Predicted band size: 69 kDa
Observed band size: 100 kDa
false
- WB
Lab
Western blot - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
MAG is a glycoprotein. The molecular weight observed is consistent with what has been described in the literature (PMID : 1716323).
Negative control : Liver (PMID : 2432614).
Exposure time : 126 seconds.
All lanes:
Western blot - Anti-MAG/GMA antibody [EPR24276-125] (<a href='/en-us/products/primary-antibodies/mag-gma-antibody-epr24276-125-ab277524'>ab277524</a>) at 1/1000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Mouse cerebellum tissue lysate at 20 µg
Lane 3:
Mouse liver tissue lysate at 20 µg
Lane 4:
Rat cerebellum tissue lysate at 20 µg
Lane 5:
Rat liver tissue 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
Predicted band size: 69 kDa
Observed band size: 100 kDa
false
- IP
Supplier Data
Immunoprecipitation - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
MAG/GMA was immunoprecipitated from 0.35 mg human cerebellum tissue lysate with ab277524 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab277524 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Human cerebellum tissue lysate 10 ug
Lane 2 : ab277524 IP in Human cerebellum tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab277524 in Human cerebellum tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 23 seconds.
All lanes:
Immunoprecipitation - Anti-MAG/GMA antibody [EPR24276-125] (<a href='/en-us/products/primary-antibodies/mag-gma-antibody-epr24276-125-ab277524'>ab277524</a>)
Predicted band size: 69 kDa
Observed band size: 100 kDa
false
- IP
Supplier Data
Immunoprecipitation - Anti-MAG/GMA antibody [EPR24276-125] - BSA and Azide free (AB277535)
This data was developed using ab277524, the same antibody clone in a different buffer formulation.
MAG/GMA was immunoprecipitated from 0.35 mg mouse brain tissue lysate with ab277524 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab277524 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse brain tissue lysate 10 ug
Lane 2 : ab277524 IP in Mouse brain tissue lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab277524 in Mouse brain tissue lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 23 seconds.
All lanes:
Immunoprecipitation - Anti-MAG/GMA antibody [EPR24276-125] (<a href='/en-us/products/primary-antibodies/mag-gma-antibody-epr24276-125-ab277524'>ab277524</a>)
Predicted band size: 69 kDa
Observed band size: 100 kDa
false
Reactivity data
Product details
ab277535 is the carrier-free version of ab277524.
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
This protein acts as an adhesion molecule that contributes to the myelination process. It exists as part of a molecular complex that interacts with other oligodendrocyte and Schwann cell proteins. This interaction is important for nerve regeneration and the expansion of the myelin sheath during development and repair. MAG also assists in signaling between axons and glial cells improving cellular communication and myelin integrity.
Pathways
MAG significantly impacts pathways such as the Nogo receptor which is associated with inhibiting axonal growth and regeneration. MAG interacts with the NOGO protein and other members of the Nogo receptor signaling pathway where it functions to regulate neuronal growth and regeneration. Furthermore MAG's interplay with NOGO receptor components contributes to limiting excessive sprouting of axons balancing growth and stability of the nervous system.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Antioxidants (Basel, Switzerland) 14: PubMed40563324
2025
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'.
For licensing inquiries, please contact partnerships@abcam.com