Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal G3BP antibody. Carrier free. Suitable for IHC-P, IP, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
G3BP, G3BP1, Ras GTPase-activating protein-binding protein 1, G3BP-1, ATP-dependent DNA helicase VIII, GAP SH3 domain-binding protein 1, hDH VIII
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Immunocytochemistry/ Immunofluorescence analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling G3BP with purified ab181150 at 1/500 dilution (0.7 μg/ml). Cells were fixed in 4% Paraformaldehyde and permeabilized with 0.1% tritonX-100. Cells were counterstained with ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1/200 (2.5 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) was used as the secondary antibody at 1/1000 (2 μg/ml) dilution. DAPI (blue) was used as nuclear counterstain. PBS instead of the primary antibody was used as the secondary antibody only control.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Immunohistochemical analysis of paraffin-embedded Human colon tissue staining G3BP using ab181150 (unpurified) at 1/100 dilution, and prediluted HRP Polymer for Rabbit IgG as a secondary antibody with Hematoxylin counterstain.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Immunofluorescent analysis of 4% paraformaldehyde fixed 293 cells staining G3BP using ab181150 (unpurified) at 1/100 dilution, and Alexa Fluor®555 stained Goat anti Rabbit IgG at 1/200 dilution as a secondary antibody (red). Dapi counterstain (blue)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Intracellular Flow Cytometry analysis of HeLa (Human cervix adenocarcinoma epithelial cell) cells labeling G3BP with purified ab181150 at 1/30 dilution (10μg/ml) (red). Cells were fixed with 4% Paraformaldehyde and permeabilised with 90% Methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1/2000. Isotype control - Rabbit monoclonal IgG (Black). Unlabeled control - Cell without incubation with primary antibody and secondary antibody (Blue).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
- IP
Supplier Data
Immunoprecipitation - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Western blot analysis of G3BP in immunoprecipitation pellets from Ramos cell lysate, using ab181151 (unpurified) at a 1/50 dilution. Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated was used as a secondary antibody at 1/1000 dilution.
All lanes:
Immunoprecipitation - Anti-G3BP antibody [EPR13986(B)] (<a href='/en-us/products/primary-antibodies/g3bp-antibody-epr13986b-ab181150'>ab181150</a>) at 1/50 dilution
All lanes:
Immunoprecipitate from Ramos cell lysate using <a href='/en-us/products/primary-antibodies/g3bp-antibody-epr13986b-ab181150'>ab181150</a>
Secondary
All lanes:
Peroxidase conjugated Goat anti-Rabbit IgG (H+L) at 1/1000 dilution
Predicted band size: 52 kDa
false
- IP
Unknown
Immunoprecipitation - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
ab181150 (purified) at 1/20 dilution (2ug) immunoprecipitating G3BP in Ramos whole cell lysate. Ramos (Human Burkitt's lymphoma B lymphocyte) whole cell lysate 10ug
Lane 2 (+) : ab181150 & Ramos whole cell lysate
Lane 3 (-) : Rabbit monoclonal IgG (ab172730) instead of ab181150 in Ramos whole cell lysate
For western blotting, VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/1000 dilution.
Blocking and diluting buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
All lanes:
Immunoprecipitation - Anti-G3BP antibody [EPR13986(B)] (<a href='/en-us/products/primary-antibodies/g3bp-antibody-epr13986b-ab181150'>ab181150</a>)
Predicted band size: 52 kDa
false
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Rat kidney tissue sections labeling G3BP with purified ab181150 at 1/50 dilution (6.86 μg/ml). Heat mediated antigen retrieval was performed using Citrate buffer, pH6.0. ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control : PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-G3BP antibody [EPR13986(B)] - BSA and Azide free (AB240247)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse kidney tissue sections labeling G3BP with purified ab181150 at 1/50 dilution (6.86 μg/ml). Heat mediated antigen retrieval was performed using Citrate buffer, pH6.0. ImmunoHistoProbe one step HRP Polymer (ready to use) was used as the secondary antibody. Negative control : PBS instead of the primary antibody. Hematoxylin was used as a counterstain.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab181150).
Related conjugates and formulations (10)
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Anti-G3BP antibody [EPR13986(B)]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-G3BP antibody [EPR13986(B)]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-G3BP antibody [EPR13986(B)]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-G3BP antibody [EPR13986(B)]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-G3BP antibody [EPR13986(B)]
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578 PE
PE Anti-G3BP antibody [EPR13986(B)]
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660 APC
APC Anti-G3BP antibody [EPR13986(B)]
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HRP Anti-G3BP antibody [EPR13986(B)]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-G3BP antibody [EPR13986(B)]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-G3BP antibody [EPR13986(B)]
Reactivity data
Product details
ab240247 is the carrier-free version of ab181150.
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
Product protocols
- Visit the General protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Journal of cellular and molecular medicine 26:5078-5094 PubMed36071546
2022
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