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Anti-C15orf41抗体
描述:

Anti-C15orf41抗体Encoding more than 700 genes, chromosome 15 is made up of approximay 106 million base pairs and is about 3% of the human genome.

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  • 厂商性质:生产厂家
  • 更新时间:2015-11-02
  • 访问量:235
产品介绍/ PRODUCT PRESENTATION

产品编号 bsyb9619R
英文名称 Anti-C15orf41抗体
中文名称 15号染色体开放阅读框41抗体
别    名 Chromosome 15 open reading frame 41; CO041_HUMAN; HH114; Hypothetical protein LOC84529; Protein HH114; Uncharacterized protein C15orf41.
 Anti-C15orf41抗体 
说 明 书 0.2ml  
研究领域 细胞生物  免疫学  神经生物学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Dog, Pig, Horse, Rabbit, 
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 32kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human C15orf41
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. The C15orf41 gene product has been provisionally designated C15orf41 pending further characterization.

 
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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