Anti-PF4 antibody [EPR26306-65] - BSA and Azide free
- BOND RX™ Validated
- KO Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal PF4 antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, Flow Cyt (Intra), IP and reacts with Mouse samples.
View Alternative Names
Cxcl4, Scyb4, Pf4, Platelet factor 4, PF-4, C-X-C motif chemokine 4
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling PF4 with ab303494 at 1/5000 (0.09 ug/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining on megakaryocytes and platelets of mouse spleen (PMID : 11468158). The section was incubated with ab303494 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 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-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Mouse pancreas tissue labeling PF4 with ab303494 at 1/5000 (0.09 ug/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Negative control : No staining on mouse pancreas.The section was incubated with ab303494 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse splenocytes cells labelling PF4 with ab303494 at 1/50 (9.0 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing cytoplasmic and membranous staining in subsets of mouse splenocytes. The image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation.Flow cytometric analysis of 2% paraformaldehyde fixed 0.1% Tween-20 permeabilized Mouse blood cells cells labelling PF4 with ab303494 at 1/500 dilution (0.1ug)/ Right (Red) compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Cells were stained with anti-CD41 conjugated to Alexa Fluor® 647. Fixed with 2% PFA for 10 min followed by intracellularly staining with rabbit IgG or ab303494.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded ((A) Bone marrow tissue from wild-type C57BL/6JGpt mice (B) Bone marrow tissue from PF4 knockout mice labeling PF4 with ab303494 at 1/5000 dilution (0.11 µg/mL), followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Antigen retrieval was heat mediated with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins. Counterstain was hematoxylin. Positive staining on (A) Bone marrow tissue from wild-type C57BL/6JGpt mice and no staining on (B) Bone marrow tissue from PF4 knockout mice. The section was incubated with ab303494 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Pf4-KO homozygous mice (Strain ID : T011518).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded (A) Spleen tissue from wild-type C57BL/6JGpt mice (B) Spleen tissue from PF4 knockout mice labeling PF4 with ab303494 at 1/5000 dilution (0.11 µg/mL), followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Antigen retrieval was heat mediated with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 20 mins. Counterstain was hematoxylin. Positive staining on (A) Spleen tissue from wild-type C57BL/6JGpt mice and no staining on (B) Spleen tissue from PF4 knockout mice. The section was incubated with ab303494 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Pf4-KO homozygous mice (Strain ID : T011518).
- WB
Lab
Western blot - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (AB303495)
This data was developed using ab303494, the same antibody clone in a different buffer formulation. Loading control : Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa) Blocking/Diluting buffer and concentration : 5% NFDM/TBST The tissue samples were kindly provided by GemPharmatech. C57BL/6JGpt wildtype mice and Pf4-KO homozygous mice (Strain ID : T011518).
Lanes 1 - 8:
Western blot - Anti-PF4 antibody [EPR26306-65] (<a href='/en-us/products/primary-antibodies/pf4-antibody-epr26306-65-ab303494'>ab303494</a>) at 1/1000 dilution
Lanes 1 - 8:
Western blot - Anti-PF4 antibody [EPR26306-65] - BSA and Azide free (ab303495)
Lane 1:
Wild-type mouse spleen tissue lysate (male)
Lane 2:
PF4 knockout spleen tissue lysate (male)
Lane 3:
Wild-type mouse spleen tissue lysate (female)
Lane 4:
PF4 knockout spleen tissue lysate (female)
Lane 5:
Wild-type mouse bone marrow tissue lysate (male)
Lane 6:
PF4 knockout bone marrow tissue lysate (male)
Lane 7:
Wild-type mouse bone marrow tissue lysate (female)
Lane 8:
PF4 knockout bone marrow tissue lysate (female)
false
Exposure time: 38s
Related conjugates and formulations (1)
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Anti-PF4 antibody [EPR26306-65]
Reactivity data
Product details
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
PF4 plays an important role in modulating the immune response and coagulation processes. PF4 is not part of a stable protein complex but can interact dynamically with heparin on the surface of endothelial cells and glycosaminoglycans. It inhibits the action of heparin promoting clot formation and angiogenesis. PF4 also attracts and activates different types of leukocytes and can regulate inflammatory processes influencing how the immune system responds to injury.
Pathways
PF4 significantly interacts with both the coagulation and inflammation pathways. In the coagulation pathway PF4 acts to neutralize heparin-like molecules thereby enhancing thrombosis. It works closely with proteins such as thrombin and fibrinogen contributing to the blood clot cascade. Within the inflammatory pathway PF4's chemokine activity helps direct leukocytes to sites of tissue damage or infection linking it to cytokines and other chemokines that mediate immune responses.
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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'.
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