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- C927
- 2025年12月22日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
蛋白表达区间:Arg28-Asn763
- 保质期：
See instructions
- 英文名：
标签:C-6His
- 库存：
表达系统:Human Cells
- 供应商：
上海经科化学科技有限公司
- 规格：
10ug/50ug/500ug/1mg
| 规格： | 10ug | 产品价格： | ￥1440.0 |
|---|---|---|---|
| 规格： | 50ug | 产品价格： | ￥4320.0 |
| 规格： | 500ug | 产品价格： | ￥19600.0 |
| 规格： | 1mg | 产品价格： | ￥28000.0 |
- The product is shipped on dry ice/polar packs.
- Upon receipt, store it immediately at the temperature listed below.
- Store at ≤-70°C, stable for 6 months after receipt.
- Store at ≤-70°C, stable for 3 months under sterile conditions after opening.
- Please minimize freeze-thaw cycles.
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文献和实验Vascular adhesion protein-1(VAP-1) is a copper amine oxidase with a topaquinone cofactor.VAP-1 is a type II integral membrane protein, but a soluble form of the enzyme is present in human serum, and its level increases in diabetes and some inflammatory liver diseases. VAP-1 catalyzes the oxidative deamination of small primary amines such as methylamine, benzylamine, and aminoAce-tone in a reaction that produces an aldehyde, ammonia, and H2O2. VAP-1 vascular expression is regulated at sites of inflammation through its release from intracellular granules in which the protein is stored. The adhesive function of VAP-1 has been demonstrated in studies showing that the protein is important for the adherence of certain lymphocyte subtypes to inflamed endothelial tissues. VAP-1 mediated adhesion is involved in the process of leukocyte extravasation, an important feature of inflammatory responses. VAP-1 is considered to be a therapeutic target for diabetes, oxidative stress, and inflammatory diseases.
Mutational Analysis of the Human Protein C Gene
The single gene for protein C is located at position q13–q14 on chromosome 2 (1 ). Two groups have described human genomic clones of protein C isolated from phage l charon libraries using cDNA for human protein C as hybridization probes
Production of Human Monoclonal Antibodies to Hepatitis C Virus and Their Characterization
Human monoclonal antibodies (hMAb) provide novel ways to probe the B-cell repertoire in health and disease. However, the development of hMAb technology has met with several difficulties owing to the instability of the cell lines, the low
Inducible microRNA-Mediated Knockdown of the Endogenous Human Lamin A/C Gene
inactivation both in vitro and in vivo. Here, the generation of a conditional RNAi cell line for microRNA (miRNA)-mediated downregulation of the endogenous lamin A/C gene is described. A tet-responsive transcription unit, encoding a designed miRNA against human
技术资料