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Anti-FAM108C1抗体

参  考  价:面议
具体成交价以合同协议为准

产品型号0.1ml/0.2ml

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所在地上海市

更新时间:2015-11-16 12:13:34浏览次数:312次

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Anti-FAM108C1抗体FAM108C1 is a 329 amino acid protein that exists as two alternatively spliced isoforms.

产品编号 yb-14692R
英文名称Anti-FAM108C1抗体
中文名称 FAM108C1蛋白抗体
别    名 abhydrolase domain containing 17C; Abhydrolase domain containing protein FAM108C1; Abhydrolase domain-containing protein FAM108C1; AB17C_HUMAN; FAM108C1; Family with sequence similarity 108 member C1.
Anti-FAM108C1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, Chicken, Pig, Cow, 
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 36kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM108C1
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:
FAM108C1 is a 329 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding FAM108C1 maps to human chromosome 15, which encodes more than 700 genes and is made up of approximay 106 million base pairs. 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 AB hydrolase superfamily. FAM108 family.

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