FITC标记的6号染色体开放阅读框81抗体
产品名称: FITC标记的6号染色体开放阅读框81抗体
英文名称: Anti-C6orf81/FITC
产品编号: HZ-15254R-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-C6orf81/FITC Conjugated antibody
FITC标记的6号染色体开放阅读框81抗体
英文名称 | Anti-C6orf81/FITC |
中文名称 | FITC标记的6号染色体开放阅读框81抗体 |
别 名 | Chromosome 6 open reading frame 81; FLJ25390; Hypothetical protein LOC221481; Uncharacterized protein C6orf81;ARM12_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, Pig, Cow, 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 | 39kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human C6orf81 |
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: Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf81 gene product has been provisionally designated C6orf81 pending further characterization. Similarity: Contains 3 ARM repeats. Database links: UniProtKB/Swiss-Prot: Q5T9G4.1 Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |
在人类基因组的近6%中,6号染色体包含1亿7000万个碱基对序列中大约1200个基因。Stutkle综合征、21羟化酶缺乏症和槭树糖浆尿病与6号染色体上的基因有关。在6号染色体Q臂上发现了双相情感障碍易感基因位点。C6OFF1基因产物已初步设计