FITC标记的IQCE蛋白抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的IQCE蛋白抗体

FITC标记的IQCE蛋白抗体

商家询价

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。