联系电话

18321282235

ac米兰app上线/ PRODUCTS PLAY

我的位置:首页  >  ac米兰app上线  >  抗体  >  ac米兰app苹果   >  Anti-CC12ORF61抗体
Anti-CC12ORF61抗体
描述:

Anti-CC12ORF61抗体Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome.

  • 产品型号:
  • 厂商性质:生产厂家
  • 更新时间:2015-11-02
  • 访问量:194
产品介绍/ PRODUCT PRESENTATION

产品编号 yb-9953R
英文名称 Anti-CC12ORF61抗体
中文名称 12号染色体开放阅读框61抗体
别    名 C12orf61; CL061_HUMAN; Putative uncharacterized protein C12orf61.
Anti-CC12ORF61抗体   
说 明 书 0.2ml  
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 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (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.
分 子 量 13kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human C12ORF61
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.

PubMed PubMed
产品介绍 background:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf61 gene product has been provisionally designated C12orf61 pending further characterization.

Database links:
UniProtKB/Swiss-Prot: Q8N7H1.1

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

留言询价/ MESSAGE INQUIRY

留言框

  • 产品:

  • 您的单位:

  • 您的姓名:

  • 联系电话:

  • 常用邮箱:

  • 省份:

  • 详细地址:

  • 补充说明:

  • 验证码:

    请输入计算结果(填写阿拉伯数字),如:三加四=7
扫码加微信
021-60514606

地址:上海市沪闵路6088号龙之梦大厦8楼806室

服务热线
18321282235

扫码加微信

Baidu
map