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Anti-CCDC93抗体
描述:

Anti-CCDC93抗体The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of

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  • 厂商性质:生产厂家
  • 更新时间:2015-10-30
  • 访问量:122
产品介绍/ PRODUCT PRESENTATION

产品编号 yb-8143R
英文名称 Anti-CCDC93抗体
中文名称 卷曲螺旋结构域蛋白93抗体
别    名 CCDC 93; Coiled-coil domain containing 93; FLJ10996; FLJ25197; MGC13033; CCD93_HUMAN.
 Anti-CCDC93抗体
说 明 书 0.1ml  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, Mouse, Rat, Dog, Pig, Cow, Sheep, 
产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=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.
分 子 量 73kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from Hu CCDC93
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.
 
PubMed PubMed
产品介绍 background:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximay 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.

Similarity:
Belongs to the CCDC93 family.

Database links:
UniProtKB/Swiss-Prot: Q567U6.2
 
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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