FITC标记的IQCE蛋白抗体
产品名称: FITC标记的IQCE蛋白抗体
英文名称: Anti-IQCE/FITC
产品编号: HZ-9018R-FITC
产品价格: null
产品产地: 中国/上海
品牌商标: HZbscience
更新时间: 2023-08-17T10:24:20
使用范围: IF=1:50-200
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Rabbit Anti-IQCE/FITC Conjugated antibody
FITC标记的IQCE蛋白抗体
产品编号 | bs-9018R-FITC |
英文名称 | Anti-IQCE/FITC |
中文名称 | FITC标记的IQCE蛋白抗体 |
别 名 | IQ domain-containing protein E; IQ motif containing E; IQCE; IQCE_HUMAN. |
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 免疫学 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, Dog, Cow, Rabbit, Sheep, |
产品应用 | IF=1:50-200 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 77kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human IQCE |
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: Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. Similarity: Contains 2 IQ domains. Database links: Entrez Gene: 23288 Human Entrez Gene: 74239 Mouse Entrez Gene: 304318 Rat SwissProt: Q6IPM2 Human SwissProt: Q6PCQ0 Mouse Unigene: 520627 Human Unigene: 179704 Mouse Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
7号染色体长约158个碱基,编码超过1000个基因,约占人类基因组的5%。第7号染色体与成骨不全、潘德红综合征、Lissencephaly、瓜氨酸血症和SuWakman钻石综合征有关。第7号染色体Q臂的缺失与威廉姆斯Bururn综合征有关,该症状以轻度智力迟钝、异常的舒适和对陌生人的友好和小精灵的外表为特征。7号染色体Q臂部分的缺失也见于许多髓系疾病中,包括急性髓性白血病和骨髓增生异常症。