Mouse Recombinant Monoclonal BRAF mutated V600E antibody. Carrier free. Suitable for WB, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
WB | IHC-P | |
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Human | Tested | Tested |
Mouse | Predicted | Predicted |
Chicken | Predicted | Predicted |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Chicken | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Chicken | Dilution info - | Notes - |
Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway (PubMed:21441910, PubMed:29433126). Phosphorylates PFKFB2 (PubMed:36402789). May play a role in the postsynaptic responses of hippocampal neurons (PubMed:1508179).
BRAF1, RAFB1, BRAF, Serine/threonine-protein kinase B-raf, Proto-oncogene B-Raf, p94, v-Raf murine sarcoma viral oncogene homolog B1
Mouse Recombinant Monoclonal BRAF mutated V600E antibody. Carrier free. Suitable for WB, IHC-P and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
The VE1 monoclonal is a sensitive antibody that detects mutated, constitutively active BRAF protein where glutamic acid is present at codon 600 instead of valine (V600E) (PubMed IDs: 21638088, 23657789).
Please be aware that non-specific nuclear staining has been reported with this antibody (PubMed IDs: 23763264, 23589031, 24838325).
ab324341 is the carrier free version of Anti-BRAF (mutated V600E) antibody [VE1] ab228461.
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.
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.
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
BRAF (mutated V600E) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Human melanoma using mouse Anti-BRAF (mutated V600E) antibody
This data was developed using Anti-BRAF (mutated V600E) antibody [VE1] ab228461, the same antibody clone in a different buffer formulation.
V600E BRAF immunohistochemistry staining of human melanoma using mouse anti-V600E BRAF antibody
Immunohistochemical analysis of formalin-fixed paraffin-embedded human melanoma tissue (carrying mutant BRAF V600E) labelling BRAF (mutated V600E) with Anti-BRAF (mutated V600E) antibody [VE1] ab228461 at 1/100 dilution. The section was pre-treated using heat-mediated antigen retrieval method with sodium citrate buffer (pH6 epitope retrieval solution 1) for 20mins. The section was then incubated with Anti-BRAF (mutated V600E) antibody [VE1] ab228461 at 1/100 dilution at room temperature and detected using a Leica BOND™ Polymer refine kit.
BRAF (mutated V600E) Western blot staining using mouse Anti-BRAF (mutated V600E) antibody
False colour image of Western blot: Anti-BRAF (mutated V600E) antibody [VE1] staining at 1/1000 dilution, shown in green; Rabbit Anti-GAPDH antibody [EPR16891] (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, Anti-BRAF (mutated V600E) antibody [VE1] ab228461 was shown to bind specifically to mutant BRAF V600E. 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-Mouse IgG H&L (IRDye® 800CW) preabsorbed and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed at 1/20000 dilution.
This image was generated in-house using a previous batch, manufactured using hybridoma production method.
All lanes: Western blot - Anti-BRAF (mutated V600E) antibody [VE1] (Anti-BRAF (mutated V600E) antibody [VE1] ab228461) at 1/1000 dilution
Lane 1: HCT 116 cell lysate (wildtype BRAF) at 20 µg
Lane 2: SW480 cell lysate (wildtype BRAF) at 20 µg
Lane 3: Caco-2 cell lysate (wildtype BRAF) at 20 µg
Lane 4: HT-29 cell lysate (mutant BRAF V600E) at 20 µg
Lane 5: A375 cell lysate (mutant BRAF V600E) at 20 µg
Lanes 1 - 5: Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed at 1/20000 dilution
Lanes 1 - 5: Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed at 1/20000 dilution
Performed under reducing conditions.
Predicted band size: 84 kDa
Observed band size: 85 kDa, 36 kDa
BRAF (mutated V600E) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of A375 cells using mouse Anti-BRAF (mutated V600E) antibody
This data was developed using Anti-BRAF (mutated V600E) antibody [VE1] ab228461, the same antibody clone in a different buffer formulation.
V600E BRAF immunohistochemistry staining of A375 cells using mouse anti-V600E BRAF antibody
IHC image of BRAF (mutated V600E) staining in a section of formalin-fixed paraffin-embedded A375 cell line (carrying mutant BRAF V600E) performed on a Leica BOND™ system using the standard protocol. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6 epitope retrieval solution 1) for 20mins. The section was then incubated with Anti-BRAF (mutated V600E) antibody [VE1] ab228461 at 5ug/ml for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.
This image was generated in-house using a previous batch manufactured using hybridoma production method.
BRAF (mutated V600E) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Caco-2 cell line using mouse Anti-BRAF (mutated V600E) antibody
This data was developed using Anti-BRAF (mutated V600E) antibody [VE1] ab228461, the same antibody clone in a different buffer formulation.
Negative control cell line image: IHC image of BRAF (mutated V600E) staining in a section of formalin-fixed paraffin-embedded Caco-2 cell line performed on a Leica BOND™ system using the standard protocol. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20mins. The section was then incubated with Anti-BRAF (mutated V600E) antibody [VE1] ab228461, 5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.
This image was generated in-house using a previous batch, manufactured using hybridoma production method.
BRAF (mutated V600E) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) staining of Human melanoma using mouse Anti-BRAF (mutated V600E) antibody
This data was developed using Anti-BRAF (mutated V600E) antibody [VE1] ab228461, the same antibody clone in a different buffer formulation.
V600E BRAF immunohistochemistry staining of human melanoma using mouse anti-V600E BRAF antibody
Immunohistochemical analysis of formalin fixed paraffin embedded human melanoma labelling BRAF (mutated V600E) with Anti-BRAF (mutated V600E) antibody [VE1] ab228461 at 1/600 dilution. The immunostaining was performed on a Ventana DISCOVERY ULTRA (Roche Tissue Diagnostics) instrument with an OptiView DAB IHC Detection Kit. Heat mediated antigen retrieval was conducted for 32 mins at 100°C with ULTRA cell conditioning solution (CC1, pH 8.5). Anti-BRAF (mutated V600E) antibody [VE1] ab228461 anti-BRAF (mutated V600E) antibody [VE1] was incubated at 37°C for 16 mins. Sections were counterstained with Hematoxylin II. Image inset shows absence of staining in secondary antibody only control.
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