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您当前的位置:首页 > 抗体 > FAM61B蛋白抗体

FAM61B蛋白抗体

  • 产品货号:mlR11001-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品货号 :  mlR11001

英文名称 :  FAM61B

中文名称 :  FAM61B蛋白抗体

    :  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.  

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 :  WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 Flow-Cyt=1μg/Test 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.

:  42kDa

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human FAM61B:251-350/385

    :  IgG

纯化方法 :  affinity purified by Protein A

:  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  :  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.

SWISS:

Q9BX40

Gene ID:

149986

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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