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货号: bs-11001R-HRP 基本售价: 2980.0 元 规格: 100ul
产品信息
- 产品编号
 - bs-11001R-HRP
 
- 英文名称
 - Anti-FAM61B/HRP
 
- 中文名称
 - 辣根过氧化物酶标记的FAM61B蛋白抗体
 
- 别 名
 - Protein FAM61B; Putative uncharacterized protein C20orf40; LSM14 homolog B (SCD6, S. cerevisiae); bA11M20.3; C20orf40; Chromosome 20 open reading frame 40; Family with sequence similarity 61 member B; LSM13; LSM14 homolog B; LSM14B SCD6 homolog B (S. cerevisiae); MGC61931; Protein LSM14 homolog B; RNA associated protein 55B; LS14B_HUMAN; LSM14B; bA11M20.3; C20orf40; FAM61B; FT005; LSM13; RAP55B.
 
- 规格价格
 - 100ul/2980元购买 大包装/询价
 
- 说 明 书
 - 100ul
 
- 研究领域
 - 细胞生物 免疫学 表观遗传学
 
- 抗体来源
 - Rabbit
 
- 克隆类型
 - Polyclonal
 
- 交叉反应
 - Human, Mouse, Rat, Dog, Cow,
 
- 产品应用
 - WB=1:50-200 ELISA=1:100-1000 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user. 
- 分 子 量
 - 42kDa
 
- 性 状
 - Lyophilized or Liquid
 
- 浓 度
 - 1mg/ml
 
- 免 疫 原
 - KLH conjugated synthetic peptide derived from human FAM61B
 
- 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.
 
- 产品介绍
 - background:
Sm and Sm-like (LSm) proteins form donut-shaped, ubiquitously expressed heptameric complexes that are involved in various steps of RNA metabolism, including RNA-protein interactions and structural changes that are required during ribosomal subunit assembly. LSm14B, also known as C20orf40, FAM61B or LSM13, is a 385 amino acid protein that exists as multiple alternatively spliced isoforms and may play a role in RNA-related events. The gene encoding LSm14B maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
Function:
May play a role in control of mRNA translation (By similarity).
Subunit:
Component of a ribonucleoprotein (RNP) complex (By similarity).
Similarity:
Belongs to the LSM14 family.
Contains 1 DFDF domain.
Database links:
UniProtKB/Swiss-Prot: Q9BX40.1
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

