FITC标记的2号染色体开放阅读框16抗体
产品名称: FITC标记的2号染色体开放阅读框16抗体
英文名称: Anti-C2orf16/FITC
产品编号: HZ-15147R-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
上海沪震实业有限公司
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- 邮编 : 200612
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Rabbit Anti-C2orf16/FITC Conjugated antibody
FITC标记的2号染色体开放阅读框16抗体
英文名称 | Anti-C2orf16/FITC |
中文名称 | FITC标记的2号染色体开放阅读框16抗体 |
别 名 | Chromosome 2 open reading frame 16; DKFZp434G118; Uncharacterized protein C2orf16; CB016_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, |
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 | 224kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human C2orf16 |
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 癈 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癈. 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 癈. |
产品介绍 | background: C2orf16 (chromosome 2 open reading frame 16), also known as DKFZp434G118 or DKFZp781D2023, is a 1,984 amino acid protein encoded by a gene that maps to human chromosome 2p23.3. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes. Database links: UniProtKB/Swiss-Prot: Q68DN1.3 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
C2orf16(染色体2开放阅读框16),也称为DKFZp434G118或DKFZp781D2023,是由一个基因编码的1984年氨基酸蛋白,该基因与人染色体2p23.3作图。染色体2作为人类第二大染色体,约占人类基因组的8%,包含2.37亿个编码1400多个基因的碱基。许多遗传疾病与2号染色体上的基因有关。HARKQUIN是一种罕见的皮肤畸形,与ABCA12基因的突变有关。脂类代谢紊乱是与ABCG5和ABCG8相关的。ALSTR综合征是一种极为罕见的隐性遗传性疾病,与ALMS1基因突变有关。染色体2包含一个可能的残留第二着丝粒以及残留端粒,这证实了人类染色体2是由两个祖先染色体的古老融合形成的假说,这两个祖先染色体仍然存在于现代猿类中。