6号染色体开放阅读框211抗体elisa实验|0.1ml/100μg 0.2ml/200μg|BJ-3999-上海邦景实业有限公司

6号染色体开放阅读框211抗体elisa实验

参考价：面议

供货周期：

现货

品牌：

GenWay

规格：

0.1ml/100μg 0.2ml/200μg

货号：

BJ-3999

CAS号：

产品详情

6号染色体开放阅读框211抗体英文名称 Anti-C6orf211

中文名称 6号染色体开放阅读框211抗体

别名 C6orf211; CF211_HUMAN; chromosome 6 open reading frame 211; UPF0364 protein C6orf211.

浓度 1mg/1ml

规格 0.2ml/200μg

抗体来源 Rabbit

6号染色体开放阅读框211抗体克隆类型 polyclonal

交叉反应 Human

产品类型一抗

研究领域细胞生物免疫学

蛋白分子量 predicted molecular weight: 51kDa

性状 Lyophilized or Liquid

免疫原 KLH conjugated synthetic peptide derived from human C6orf211

亚型 IgG

纯化方法 affinity purified by Protein A

储存液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4

产品应用 WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500

（石蜡切片需做抗原修复）

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

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.

Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

产品介绍 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 6号染色体开放阅读框211抗体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 C6orf211 gene product has been provisionally designated C6orf211 pending further characterization.

Similarity : Belongs to the UPF0364 family.

Database links : UniProtKB/Swiss-Prot: Q9H993.1