Pig Von Willebrand Factor (vWF) Peptide (OVA)
442€ (100 µg)
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name
Pig Von Willebrand Factor (vWF) Peptide (OVA)
category
Proteins and Peptides
provider
Abbexa
reference
abx651837
tested applications
WB, SDS-PAGE
Description
Von Willebrand Factor (vWF) Peptide (OVA) is a protein from Pig.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Proteins and Peptides |
| Immunogen Target | Von Willebrand Factor (vWF) |
| Origin | Pig |
| Conjugation | OVA |
| Observed MW | Molecular Weight: Calculated MW: 2026.4 Da Concentration: Prior to lyophilization: 200 µg/ml |
| Expression | Synthetic |
| Purity | > 97% |
| Size 1 | 100 µg |
| Size 2 | 200 µg |
| Size 3 | 500 µg |
| Size 4 | 1 mg |
| Size 5 | 5 mg |
| Form | Lyophilized To keep the original salt concentration, we recommend reconstituting to the original concentration prior to lyophilization (see Concentration) in ddH2O. If a lower concentration is required, dilute in PBS, pH 7.4. If a higher concentration is required, the product can be reconstituted directly in PBS, pH 7.4, though please note that this will change the overall salt concentration. The stock concentration should be between 0.1-1.0 mg/ml. Do not vortex. |
| Tested Applications | WB, SDS-PAGE |
| Buffer | Prior to lyophilization: PBS, pH 7.4, containing 0.01% Sarcosyl, 1 mM DTT, 5% Trehalose and Proclin-300. |
| Availability | Shipped within 5-15 working days. |
| Storage | Store at 2-8 °C for up to one month. Store at -80 °C for up to one year. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q28833 |
| Background | Protein vWF |
| Status | RUO |
| Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
Related Products
von Willebrand Factor (vWF) Antibody
vWF Antibody is a Rabbit Polyclonal antibody against vWF. The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008].
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