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FAM49B蛋白抗体价格

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  • 南京森贝伽生物科技有限公司
  • 2014-03-27 11:42:51
  • 南京市
  • 南京
  • 1274

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【简单介绍】

FAM49B蛋白抗体由南京森贝伽长期现货供应,我司为您提供该产品的规格、价格、说明书等,公司产品种类齐全,生产的抗体每个流程都执行严格的检测标准,如需了解更多均可与我司销售人员,我们将竭诚为您服务。

【详细说明】

FAM49B蛋白抗体是我司为您提供的高品质抗体,公司生产的每一个抗体都经过严格检测和稳定性测试,保证了结果的准确性、敏感性、特异性。公司产品质量有保证,*,为广大客户提供完善的售前、售中、售后服务,公司生产的产品也已获得广大客户的信赖。南京森贝伽生物科技有限公司为服务更多科研工作者的需要公司现经营抗体、ELISA试剂盒、标准品、染色液、染色试剂盒、培养基等多种科研产品,如有需要可与我司销售人员。
英文名称 FAM49B
中文名称 FAM49B蛋白抗体
别    名 BM 009; FA49B_HUMAN; Fam49b; Family with sequence similarity 49, member B; L1; Protein FAM49B.    
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, 
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.
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human FAM49B
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
FAM49B蛋白抗体保存条件 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
FAM49B蛋白抗体产品介绍 background:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM49B gene product has been provisionally designated FAM49B pending further characterization.

Similarity:
Belongs to the FAM49 family.

Database links:

Entrez Gene: 51571 Human

SwissProt: Q9NUQ9 Human

Unigene: 126941 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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