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Anti-DTWD1抗体
描述:

Anti-DTWD1抗体Encoding more than 700 genes, chromosome 15 is made up of approximay 106 million base pairs and is about

  • 产品型号:
  • 厂商性质:生产厂家
  • 更新时间:2015-11-12
  • 访问量:38
产品介绍/ PRODUCT PRESENTATION

产品编号 yb-14436R
英文名称 Anti-DTWD1抗体
中文名称 DTWD1蛋白抗体
别    名 DTW domain containing 1; DTW domain-containing protein 1; Dtwd1; DTWD1_HUMAN; MDS009; x 009 protein.
 Anti-DTWD1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, Mouse, Rat, Pig, Cow, Horse, Sheep, 
产品应用 WB=1:100-500 ELISA=1:500-1000 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.
分 子 量 35kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human DTWD1
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 more than 700 genes, chromosome 15 is made up of approximay 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Similarity:
Belongs to the DTW family.

Gene ID:
56986

Database links:

Entrez Gene: 56986 Human

SwissProt: Q8N5C7 Human

Unigene: 127432 Human


 
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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