Anti-Von Willebrand Factor抗体[F8/86] (ab778)
概述
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产品名称Anti-Von Willebrand Factor抗体[F8/86]
参阅全部 Von Willebrand Factor 一抗 -
描述小鼠单克隆抗体[F8/86] to Von Willebrand Factor
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宿主Mouse
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经测试应用适用于: IHC-P, IHC-Frmore details
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种属反应性与反应: Human
预测可用于: Rabbit
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免疫原
Von Willebrand Factor isolated from human plasma.
性能
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形式Liquid
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存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C or -80°C. Avoid freeze / thaw cycle.
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存储溶液Preservative: 0.05% Sodium azide
Constituents: Tissue culture supernatant, 1% BSA -
纯度Tissue culture supernatant
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克隆单克隆
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克隆编号F8/86
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同种型IgG1
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轻链类型kappa
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研究领域
相关产品
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Compatible Secondaries
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Isotype control
应用
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.
| 应用 | Ab评论 | 说明 |
|---|---|---|
| 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. |
靶标
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功能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.
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组织特异性Plasma.
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疾病相关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.
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序列相似性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. -
结构域The von Willebrand antigen 2 is required for multimerization of vWF and for its targeting to storage granules.
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翻译后修饰All cysteine residues are involved in intrachain or interchain disulfide bonds.
N- and O-glycosylated. -
细胞定位Secreted. Secreted > extracellular space > extracellular matrix. Localized to storage granules.
- Information by UniProt
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数据库链接
- Entrez Gene: 7450 Human
- Omim: 613160 Human
- SwissProt: P04275 Human
- Unigene: 440848 Human
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别名
- Coagulation factor VIII antibody
- Coagulation factor VIII VWF antibody
- F8VWF antibody
see all
图片
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![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Von Willebrand Factor antibody [F8/86] (ab778)](https://www.abcam.cn/ps/products/0/ab778/Images/ab778_1.jpg)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Von Willebrand Factor antibody [F8/86] (ab778)Formalin fixed paraffin embedded human tonsil stained with Von Willebrand Factor using ABC and AEC chromogen.
文献
This product has been referenced in:
- Zhang W et al. Cell-free therapy based on adipose tissue stem cell-derived exosomes promotes wound healing via the PI3K/Akt signaling pathway. Exp Cell Res 370:333-342 (2018). Read more (PubMed: 29964051) »
- Chen JH et al. Protective effects of atorvastatin on cerebral vessel autoregulation in an experimental rabbit model of subarachnoid hemorrhage. Mol Med Rep 17:1651-1659 (2018). Read more (PubMed: 29257200) »
