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Read our guarantee »Products:Cardiovascular >> Blood >> Serum Proteins
Anti-Von Willebrand Factor antibody [F8/86]
See all Von Willebrand Factor products (23) ...
Mouse monoclonal [F8/86] to Von Willebrand Factor
This antibody reacts with Von Willebrand Factor in endothelial cells. It also reacts with megakaryocytes in human bone marrow. Please note this antibody has been cited as worked in Rabbit in PMID 18387175 but due to customer concerns regarding this we have changed it to predicted species.
IHC-P, IHC-Frmore details
Reacts with
Human
Predicted to work with
Rabbit
Von Willebrand Factor isolated from human plasma.
Liquid
Store at +4°C.
Preservative: 0.05% Sodium Azide
Constituents: 1% BSA, Tissue culture supernatant
Tissue culture supernatant
Monoclonal
F8/86
IgG1
kappa
Stem Cells >> Endothelial Progenitors >> Endothelial Markers
Cancer >> Invasion/microenvironment >> Angiogenesis >> Angiogenic growth factors
Cardiovascular >> Blood >> Coagulation >> Regulatory
Cardiovascular >> Blood >> Coagulation >> Extrinsic
Cardiovascular >> Blood >> Platelets
Cardiovascular >> Blood >> Serum Proteins
Immunohistochemistry (Formalin-fixed paraffin-embedded sections) - Von Willebrand Factor antibody [F8/86] (ab778)
(enlarge)
Our Abpromise guarantee covers the use of ab778 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: 1/15 - 1/30.Perform enzymatic antigen retrieval before commencing with IHC staining protocol.
IHC-Fr: 1/15 - 1/30.(ABC method. We suggest an incubation period of 60 minutes at room temperature.)
Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet-surface receptor complex GPIb-IX-V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma.
Plasma.
Defects in VWF are the cause of von Willebrand disease (VWD) [MIM:277480]. VWD defines a group of hemorrhagic disorders in which the von Willebrand factor is either quantitatively or qualitatively abnormal resulting in altered platelet function. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII and impaired platelet adhesion. Type I von Willebrand disease is the most common form and is characterized by partial quantitative plasmatic deficiency of an otherwise structurally and functionally normal Willebrand factor; type II is associated with a qualitative deficiency and functional anomalies of the Willebrand factor; type III is the most severe form and is characterized by total or near-total absence of Willebrand factor in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII.
Contains 1 CTCK (C-terminal cystine knot-like) domain.
Contains 4 TIL (trypsin inhibitory-like) domains.
Contains 3 VWFA domains.
Contains 3 VWFC domains.
Contains 4 VWFD domains.
The von Willebrand antigen 2 is required for multimerization of vWF and for its targeting to storage granules.
All cysteine residues are involved in intrachain or interchain disulfide bonds.
N- and O-glycosylated.
Secreted. Secreted > extracellular space > extracellular matrix. Localized to storage granules.
Target information above from: UniProt accessionP04275
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunohistochemistry (Formalin-fixed paraffin-embedded sections) - Von Willebrand Factor antibody [F8/86] (ab778)
![Immunohistochemistry (Formalin-fixed paraffin-embedded sections) - Von Willebrand Factor antibody [F8/86] (ab778)](/ps/datasheet/Images/0/ab778/ab778_1.jpg)
Formalin fixed paraffin embedded human tonsil stained with Von Willebrand Factor using ABC and AEC chromogen.
This product has been referenced in:
See all 3 publications for this product
Publishing research using ab778? Please let us know so that we can cite the reference in this datasheet
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
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