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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Lyophilized from a solution in 20 mM Tris-HCl pH 8.0, 100 mM NaCl,1mM EDTA, 4%trehalose,2134% mannitol.
- 保质期:
1 year
- 英文名:
Recombinant PEDV S1/Spike glycoprotein 1 Protein, N-His
- 库存:
999
- 供应商:
abinscience
- 规格:
50ug

| Product name | Recombinant PEDV S1/Spike glycoprotein 1 Protein, N-His |
|---|---|
| Catalog No. | VK564032 |
| Form | Lyophilized |
| Storage buffer | Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol. |
| Purity | >90% as determined by SDS-PAGE. |
| Applications | ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress |
| Endotoxin level | Please contact with the lab for this information. |
| Expression system | E. coli |
| Accession | Q91AV1 |
| Protein length | Cys26-His734 |
| Nature | Recombinant |
| Predicted molecular weight | 80.05 kDa |
| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. |
| Alternative Names | Spike glycoprotein, S glycoprotein, E2, Peplomer protein, S, S1, Spike glycoprotein 1 (strain CV777) |
| Species | Porcine epidemic diarrhea virus (strain CV777) (PEDV) |
| Note | For research use only. |
Abinscience, founded in 2023 and located in the innovation technology center in Strasbourg, France, is the core research reagent brand of ProteoGenix. Focusing on the development and production of life science research reagents, Abinscience takes "Empowering Bioscience Discovery" as its vision, and is committed to providing high-quality and innovative biological reagent products and technical solutions for global researchers.
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文献和实验Characterization of the Dengue Virus Envelope Glycoprotein Expressed in Pichia pastoris
The full-length and truncated forms of recombinant envelope (E) glycoprotein from Dengue virus type 1, Singapore strain S275/90 were expressed in the yeast, Pichia pastoris , using a secretory vector. A truncated form of the E protein
. The secreted recombinant GST-F2 /F1 protein was further analysed using glycosidases. Our results showed that the GST-F2 /F1 protein were sensitive to peptide: N -glycosidase F (PNGase F) treatment, but not to Endoglycosidase H (EndoH) treatment. This indicates
Metabolic engineering of mammalian cells for optimized glycosylation is usually done to improve activity and the pharmacokinetic features of glycoprotein therapeutics. The field is mainly focused around engineering of N -glycans
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