Anti-INPP5E/FITC Conjugated抗体
产品名称： Anti-INPP5E/FITC Conjugated抗体
英文名称： Anti-INPP5E/FITC
产品编号： YB--4487R-FITC
产品价格： null
产品产地： 中国/美国
品牌商标： Ybscience
更新时间： 2023-08-17T10:29:50
使用范围： 科研使用
上海钰博生物科技有限公司
- 联系人 : 陈环环
- 地址 : 上海市沪闵路6088号龙之梦大厦8楼806室
- 邮编 : 200612
- 所在区域 : 上海
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- 传真 : 021-60514606
- 邮箱 : shybio@126.com
Anti-INPP5E/FITC Conjugated抗体
| 产品编号 | YB-4487R-FITC |
| 英文名称 | Anti-INPP5E/FITC |
| 中文名称 | FITC标记的聚磷酸肌醇磷酸酶5E抗体 |
| 别 名 | Inositol polyphosphate-5-phosphatase E; Inositol polyphosphate 5 phosphatase E; 72 kDa inositol polyphosphate 5-phosphatase; Phosphatidylinositol 4,5-bisphosphate 5-phosphatase; INP5E_HUMAN; Phosphatidylinositol polyphosphate 5-phosphatase type IV. |
| 规格价格 | 100ul/2980元 购买 大包装/询价 |
| 说 明 书 | 100ul |
| 研究领域 | 细胞生物 发育生物学 神经生物学 信号转导 激酶和磷酸酶 |
| 抗体来源 | Rabbit |
| 克隆类型 | Polyclonal |
| 交叉反应 | Human, Mouse, Rat, Dog, Rabbit, |
| 产品应用 | ICC=1:50-200 IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 70kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human INPP5E |
| 亚 型 | IgG |
| 纯化方法 | affinity purified by Protein A |
| 储 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
| 保存条件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 产品介绍 | background: Converts phosphatidylinositol 3,4,5-trisphosphate (PtdIns 3,4,5-P3) to PtdIns-P2. Specific for lipid substrates,inactive towards water soluble inositol phosphates. DISEASE: Mental retardation, truncal obesity, retinal dystrophy, and micropenis (MORMS) [MIM:610156]: An autosomal recessive disorder characterized by moderate mental retardation, truncal obesity, congenital non-progressive retinal dystrophy, and micropenis in males. The phenotype is similar to Bardet-Biedl syndrome and Cohen syndrome Distinguishing features are the age of onset, the non-progressive nature of the visual impairment, lack of dysmorphic facies, skin or gingival infection, microcephaly, mottled retina, polydactyly, and testicular anomalies. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the inositol 1,4,5-trisphosphate 5-phosphatase type IV family. Database links: Entrez Gene: 22876 Human Entrez Gene: 101490 Mouse Entrez Gene: 309008 Rat Omim: 609389 Human SwissProt: Q9Y2H2 Human SwissProt: Q8CDA1 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |