FITC标记的7号染色体开放阅读框42抗体
产品名称： FITC标记的7号染色体开放阅读框42抗体
英文名称： Anti-C7orf42/FITC
产品编号： HZ-15266R-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： ICC=1:50-200 IF=1:50-200
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Rabbit Anti-C7orf42/FITC Conjugated antibody
FITC标记的7号染色体开放阅读框42抗体
| 英文名称 | Anti-C7orf42/FITC |
| 中文名称 | FITC标记的7号染色体开放阅读框42抗体 |
| 别 名 | C7orf42; TM248_HUMAN; Chromosome 7 open reading frame 42; FLJ10099; FLJ13090; Hypothetical protein LOC55069; UPF0458 protein C7orf42. |
| 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, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, |
| 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 | 35kDa |
| 性 状 | Lyophilized or Liquid |
| 浓 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human C7orf42 |
| 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 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. The C7orf42 gene product has been provisionally designated C7orf42 pending further characterization. Subcellular Location: Membrane; Multi-pass membrane protein (Potential). Similarity: Belongs to the TMEM248 family. Database links: UniProtKB/Swiss-Prot: Q9NWD8.1 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
染色体7与成骨不全、Pendred综合征、Lissencephaly、瓜氨酸血症和Shwachman-Diamond综合征有关。第7号染色体q臂部分缺失与威廉姆斯-贝伦综合征有关，这种症状的特征是轻度智力低下、与陌生人异常的舒适和友好以及外表苗条。在包括急性髓细胞白血病和骨髓增生异常在内的许多髓系疾病中，也能看到7号染色体q臂部分缺失。C7ORF42基因产物已暂时指定为C7OF42，有待进一步鉴定。