Anti-GPVI antibody [EPR25283-14] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GPVI antibody. Carrier free. Suitable for IHC-P, IP, Flow Cyt, WB, IHC-Fr and reacts with Mouse samples.
View Alternative Names
Platelet glycoprotein VI, GPVI, Glycoprotein 5, Gp6
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling GPVI with ab289964 at 1/500 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Negative control : no staining on mouse cerebrum PMID 10961879). The section was incubated with ab289964 at 4°C overnight. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0).
- Flow Cyt
Lab
Flow Cytometry - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of Mouse blood cells cells labelling GPVI with ab289964 at 1/500 dilution (0.1μg)(Right) compared with a Rabbit monoclonal IgG (ab172730) isotype control (Left). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) was used as secondary antibody at 1/2000 dilution. Cells were stained with rabbit IgG or ab289964. Then stained with anti-CD41 conjμgated to APC. Gated on viable cells.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling GPVI with ab289964 at 1/500 dilution followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Cytoplasmic staining on megakaryocytes and platelets of mouse spleen. The section was incubated with ab289964 at 4°C overnight. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0).
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh) tissue labeling GPVI with ab289964 at 1/100 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Negative control (PMID : 10961879). No staining on mouse cerebellum is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh) tissue labeling GPVI with ab289964 at 1/100 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Positive staining in megakaryocytes of mouse spleen is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IP
Lab
Immunoprecipitation - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using ab289964, the same antibody clone in a different buffer formulation.
GPVI was immunoprecipitated from Mouse platelet lysate with ab289964 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289964 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Mouse platelet lysate 10 μg
Lane 2 : ab289964 IP in Mouse platelet lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289964 in mouse platelet lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 15 seconds
The expression profile/ molecμlar weight observed is consistent with what has been described in the literature (PMID : 23112346, PMID : 9295288).
All lanes:
Immunoprecipitation - Anti-GPVI antibody [EPR25283-14] (<a href='/en-us/products/primary-antibodies/gpvi-antibody-epr25283-14-ab289964'>ab289964</a>)
Predicted band size: 37 kDa
Observed band size: 58 kDa
false
- WB
Lab
Western blot - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using 289964, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : �23112346, PMID : �16014566 ).
114 seconds
Exposure time :
All lanes:
Western blot - Anti-GPVI antibody [EPR25283-14] (<a href='/en-us/products/primary-antibodies/gpvi-antibody-epr25283-14-ab289964'>ab289964</a>) at 1/1000 dilution
Lane 1:
Mouse platelet treated with PNGase F lysate at 20 µg
Lane 2:
Mouse platelet lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 37 kDa
Observed band size: 34 kDa,58 kDa
false
- WB
Lab
Western blot - Anti-GPVI antibody [EPR25283-14] - BSA and Azide free (AB289987)
This data was developed using 289964, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 23112346, 16014566).
Negative control : cerebellum. (PMID : 10961879).
Exposure time : 70 seconds.
All lanes:
Western blot - Anti-GPVI antibody [EPR25283-14] (<a href='/en-us/products/primary-antibodies/gpvi-antibody-epr25283-14-ab289964'>ab289964</a>) at 1/1000 dilution
Lane 1:
Mouse platelet lysate at 20 µg
Lane 2:
Mouse cerebellum tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 37 kDa
Observed band size: 58 kDa
false
Related conjugates and formulations (1)
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Anti-GPVI antibody [EPR25283-14]
Reactivity data
Product details
ab289987 is the carrier-free version of ab289964.
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
The target participates in the formation of platelet activation complexes. GPVI partners with the Fc receptor γ-chain to transmit activation signals upon collagen binding. This process results in platelet shape change granule secretion and aggregation which are all critical steps for clot formation. By interacting with collagen GPVI ensures that platelets can effectively respond to vascular damage particularly in arterial vessels where high shear forces prevail.
Pathways
The glycoprotein VI contributes significantly to the immune and coagulation pathways. It activates the enzyme Syk kinase following collagen binding which further triggers the downstream signaling pathways like the MAPK pathway leading to platelet activation. GPVI works closely with other receptors like integrin α2β1 and the glycoprotein Ib/V/IX complex reinforcing platelet-collagen interactions and stabilizing the platelet plug formation during thrombus growth.
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