VWF
Description
von Willebrand factor
Also known as
F8VWF, VWD
Species
Homo sapiens
Entrez ID
7450
MGC ID
GU014837
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Log in to manage alertsPlasmids containing this gene, or a homologous gene.
| ID | Plasmid | Gene/Insert | PI |
|---|---|---|---|
| 53419 | VWF-bio-His | VWF (Homo sapiens) | Wright |
| 59577 | ReaLiSM A1-43-GPIba+2cys | VWF A1-linker-GPIba (Homo sapiens) | Springer |
| 59580 | ReaLiSM A1-26link-GPIba+2cys | VWF A1-linker-GPIba (Homo sapiens) | Springer |
| 59581 | ReaLiSM A1-Hinge-GPIba+2cys | VWF A1-linker-GPIba (Homo sapiens) | Springer |
| 64847 | pRSET-XS-VWF | Venus_VWF A2 domain aa 1594-1670_Cerulean_TEV_7X His (Homo sapiens) | Neelamegham |
| 64856 | pRSET-A2-77p-Venus | VWF A2 domain aa 1594-1670_TEV_Venus_7X His (Homo sapiens) | Neelamegham |
| 124794 | pcDNA3.1-WT-VWF | VWF (Homo sapiens) | Neelamegham |
| 124823 | pcDNA3.1-deltaA1-VWF | VWF without A1 domain (Homo sapiens) | Neelamegham |
| 124824 | pcDNA3.1-deltaA1-Lock-VWF | VWF without A1 domain and Lock A2 domain (Homo sapiens) | Neelamegham |
| 124825 | pcDNA3.1-deltaA1-D1498A-VWF | VWF without A1 domain and D1498A mutation A2 domain (Homo sapiens) | Neelamegham |
| 124826 | pcDNA3.1-deltaA1-R1597W-VWF | VWF without A1 domain and R1597W mutation A2 domain (Homo sapiens) | Neelamegham |
| 124827 | pCS-CG-WT-Cer-VWF | VWF with cyan fluorescent protein fusion between D'D3 and A1 domains (Homo sapiens) | Neelamegham |
| 124828 | pCS-CG-Lock-Cer-VWF | VWF with cyan fluorescent protein fusion between D'D3 and A1 domains and Lock A2 domain (Homo sapiens) | Neelamegham |