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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
细胞色素 P450 还原酶单克隆抗体(兔源)
- 抗体英文名:
Cytochrome P450 reductase Antibody, mAb, Rabbit
- 靶点:
细胞色素 P450 还原酶
- 浓度:
0.5mg/mL(常规浓度,以官方说明书为准)
- 应用范围:
Western Blot、免疫细胞化学 / 免疫荧光 (ICC/IF)、免疫组化 (IHC)、免疫沉淀 (IP)
- 宿主:
兔(Rabbit)
- 适应物种:
人、小鼠、大鼠
- 保质期:
- 20℃可稳定保存 半 年
- 抗原来源:
人细胞色素 P450 还原酶来源合成肽
- 级别:
科研级
- 库存:
现货
- 供应商:
上海经科化学科技有限公司
- 标记物:
无(Unconjugated)
- 克隆性:
单克隆(Monoclonal)
- 保存条件:
-20℃,可稳定保存 半 年
- 形态:
液体(Liquid)
- 亚型:
Rabbit IgG
- 免疫原:
人细胞色素 P450 还原酶来源合成肽
- 规格:
50μl/100μl
| 规格: | 50μl | 产品价格: | ¥1200.0 |
|---|---|---|---|
| 规格: | 100μl | 产品价格: | ¥2200.0 |
| Specificity | This product is specific to Cytochrome P450 reductase |
| Host Species | Rabbit |
| Immunogen | A synthesized peptide derived from human Cytochrome P450 reductase |
| Species Reactivity | Human; Mouse; Rat |
| Conjugate | Unconjugated |
| Form | Liquid |
| Storage Buffer | Supplied in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol. |
| Storage Instructions | Store at -20°C. This product is stable for 1 year upon receipt, when handled and stored as instructed. |
| Purification | Affinity-chromatography |
| Isotype | Rabbit IgG |
| Clonality | Monoclonal |
| Target Background | This enzyme is required for electron transfer from NADP to cytochrome P450 in microsomes. It can also provide electron transfer to heme oxygenase and cytochrome B5. |
| Synonyms | CPR; CYPOR; P450R; por; |
Cytochrome P450 reductase 抗体、细胞色素 P450 还原酶抗体、POR 抗体、兔源 Cytochrome P450 reductase 抗体、单克隆 Cytochrome P450 reductase 抗体、抗 Cytochrome P450 reductase 抗体、药物代谢相关抗体、氧化还原相关抗体、WB 抗体、IHC 抗体、IF 抗体、ELISA 抗体
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文献和实验Cytochrome P450 Reconstitution Systems
adenine dinucleotide phosphate-cytochrome P450 reductase in the membranes of phospholipid vesicles. However, our studies have suggested that the conditions for reconstitution of activities vary depending on the P450 enzymes used. For example
Nanoscale-Engineered Cytochrome P450 System with a Branch Structure
Most of the bacterial cytochrome P450 s require two kinds of electron transfer proteins, ferredoxin and ferredoxin reductase, and thus P450 s do not show catalytic activity by themselves. A microbial transglutaminase-mediated site-specific
Isolation and Purification of Constitutive Forms of Microsomal Cytochrome P450
from microsomes through the use of proteases were not successful, resulting merely in the solubilization of a number of other microsomal proteins. The breakthrough event was the solubrlizatron of rabbit liver microsomal cytochrome P450 using the ionic detergent
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