- 询价
- 博湖
- 0.47-30ng/ml
- 进口、国产
- BHE97257
- 2025年07月11日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
上海博湖
- 检测范围：
0.47-30ng/ml
- 检测方法：
Sandwich ELISA, Double Antibody
- 应用：
0.281ng/ml
- 样本：
INTX
- 规格：
96T
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文献和实验N-Linked Glycan Characterization of Heterologous Proteins
-linked glycosylation site, a His-tagged Kringle 3 domain of human plasminogen (K3), was used to identify combinations of optimal leader/catalytic domain(s) to recreate human N-glycan processing in the Pichia system. In this chapter we describe detailed
The Use of TAGZyme for the Efficient Removal of N-Terminal His-Tags
is unwanted or may represent a disadvantage for the projected use of the protein, like in clinical, functional or structural studies. For N-terminal tags, the TAGZyme system represents an ideal approach for fast and accurate tag removal. TAGZyme is based
Fabrication of a Human Recombinant Collagen-Based Corneal Substitute Using Carbodiimide Chemistry
Human recombinant collagen can be cross-linked with a variety of chemical cross-linking agents. Cross-linking methods can be tuned to confer collagen-based scaffolds with specific physical properties, improved antigenicity and thermal
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