FITC标记的6号染色体开放阅读框146抗体-抗体-抗体-生物在线
FITC标记的6号染色体开放阅读框146抗体

FITC标记的6号染色体开放阅读框146抗体

商家询价

产品名称: FITC标记的6号染色体开放阅读框146抗体

英文名称: Anti-C6orf146/FITC

产品编号: HZ-15223R-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-C6orf146/FITC Conjugated antibody

FITC标记的6号染色体开放阅读框146抗体

 

英文名称 Anti-C6orf146/FITC
中文名称 FITC标记的6号染色体开放阅读框146抗体
别    名 Chromosome 6 open reading frame 146; Hypothetical protein LOC222826; MGC43581; Uncharacterized protein C6orf146.   
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.
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C6orf146
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. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf146 gene product has been provisionally designated C6orf146 pending further characterization.

Similarity:
Belongs to the FAM217 family.

Database links:

Entrez Gene: 222826 Human

SwissProt: Q8IXS0 Human

SwissProt: Q9D9W6 Mouse

SwissProt: Q5XHY8 Rat



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。6号染色体q臂部分缺失与早期发病的肠癌有关,提示存在癌症易感位点。迟发性皮肤卟啉症通过HFE基因与6号染色体相关联,当HFE基因突变时,它使个体易于发展这种卟啉症。值得注意的是,与帕金森病相关的PARK2基因以及编码主要组织相容性复合蛋白的基因也位于第6染色体上,这些蛋白是免疫系统的关键分子组成部分并且决定了风湿病的易感性。Stutkle综合征、21羟化酶缺乏症和枫糖浆尿病也与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。C6ORF 146基因产物已暂时指定为C6ORF 146,有待进一步鉴定。