Human Von Willebrand Factor ELISA Kit (ab223864)
製品の概要
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製品名Human Von Willebrand Factor ELISA Kit
Von Willebrand Factor キット 製品一覧 -
検出方法Colorimetric
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再現性
Intra-Assay（同時再現性） サンプル N 平均値 SD CV% Serum 3 3.4% Inter-Assay（日差再現性） サンプル N 平均値 SD CV% Serum 5 6.4% -
サンプルの種類Serum, Heparin Plasma, EDTA Plasma, Citrate Plasma
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アッセイタイプSandwich (quantitative)
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検出感度0.079 ng/ml
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検出範囲0.469 ng/ml - 30 ng/ml
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添加回収試験
特定サンプルでの回収試験 サンプルの種類 平均 % 測定範囲 Serum 101 94% - 107% Cell culture media 88 80% - 95% Heparin Plasma 95 89% - 102% EDTA Plasma 92 86% - 97% Citrate Plasma 98 83% - 118% -
全工程の試験時間1h 30m
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ステップOne step assay
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種交差性交差種: Human, Rhesus monkey
非交差種: Mouse, Rat, Cow -
製品の概要
Human Von Willebrand Factor SimpleStep ELISA® kit (ab189571) has been re-developed with new capture and detector antibodies. This new kit has the same name but a different product number (ab223864). We have identified new recombinant monoclonal antibodies to use in the SimpleStep ELISA platform that provide a higher sensitivity when quantifying Von Willebrand Factor in human serum, plasma and cell culture supernatant samples.
Von Willebrand Factor in vitro SimpleStep ELISA® (Enzyme-Linked Immunosorbent Assay) kit is designed for the quantitative measurement of Von Willebrand Factor protein in human serum, plasma and cell culture supernatant samples.
The SimpleStep ELISA® employs an affinity tag labeled capture antibody and a reporter conjugated detector antibody which immunocapture the sample analyte in solution. This entire complex (capture antibody/analyte/detector antibody) is in turn immobilized via immunoaffinity of an anti-tag antibody coating the well. To perform the assay, samples or standards are added to the wells, followed by the antibody mix. After incubation, the wells are washed to remove unbound material. TMB substrate is added and during incubation is catalyzed by HRP, generating blue coloration. This reaction is then stopped by addition of Stop Solution completing any color change from blue to yellow. Signal is generated proportionally to the amount of bound analyte and the intensity is measured at 450 nm. Optionally, instead of the endpoint reading, development of TMB can be recorded kinetically at 600 nm.
Von Willebrand Factor is critical 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. Von Willebrand Factor 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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アプリケーション適用あり: Sandwich ELISAmore details
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試験プラットフォームMicroplate (12 x 8 well strips)
製品の特性
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保存方法Store at +4°C. Please refer to protocols.
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内容 1 x 96 tests 10X Wash Buffer PT (ab206977) 1 x 20ml Antibody Diluent 5BI 1 x 6ml Human Von Willabrand Factor Capture Antibody Lyophilized 1 vial Human Von Willabrand Factor Detector Antibody 10X 1 x 600µl Human Von Willabrand Factor Lyophilized Recombinant Protein 2 vials Plate Seals 1 unit Sample Diluent NS 1 x 50ml SimpleStep Pre-Coated 96-Well Microplate (ab206978) 1 unit Stop Solution 1 x 12ml TMB Development Solution 1 x 12ml -
研究分野
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機能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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組織特異性Plasma.
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関連疾患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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配列類似性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. -
ドメインThe von Willebrand antigen 2 is required for multimerization of vWF and for its targeting to storage granules.
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翻訳後修飾All cysteine residues are involved in intrachain or interchain disulfide bonds.
N- and O-glycosylated. -
細胞内局在Secreted. Secreted > extracellular space > extracellular matrix. Localized to storage granules.
- Information by UniProt
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別名
- Coagulation factor VIII
- Coagulation factor VIII VWF
- F8VWF
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参照データベース
- Entrez Gene: 7450 Human
- Omim: 613160 Human
- SwissProt: P04275 Human
- Unigene: 440848 Human
関連製品
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Alternative Versions
アプリケーション
Our Abpromise guarantee covers the use of ab223864 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| アプリケーション | Abreviews | 特記事項 |
|---|---|---|
| Sandwich ELISA | Use at an assay dependent concentration. |
画像
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Example of human Von Willebrand Factor standard curve in Sample Diluent NSBackground-subtracted data values (mean +/- SD) are graphed.
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Interpolated concentrations of native Von Willebrand Factor in human serum and plasma samplesThe concentrations of Von Willebrand Factor were measured in duplicates, interpolated from the Von Willebrand Factor standard curves and corrected for sample dilution. Undiluted samples are as follows: serum 1:500, plasma (citrate) 1:500, plasma (heparin) 1:500, and plasma (EDTA) 1:500. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean Von Willebrand Factor concentration was determined to be 4.226 µg/mL in neat serum, 2.793 µg/mL in neat plasma (citrate), 1.774 µg/mL in neat plasma (heparin), and 2.819 µg/mL in neat plasma (EDTA).
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Serum from ten individual healthy human female donors was measured in duplicateInterpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean Von Willebrand Factor concentration was determined to be 5.280 µg/mL with a range of 2.088 – 11.35 µg/mL.
プロトコール
参考文献
ab223864 has not yet been referenced specifically in any publications.
