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.