产品货号 :  mlR18813

英文名称 :  METTL15/METT5D1

中文名称 :  甲基样蛋白15抗体

别    名 :  Methyltransferase 5 domain containing 1; METT5D 1.  

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, Pig, Sheep,

产品应用 :  ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 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 :  46kDa

细胞定位 :  细胞核

性    状 :  Lyophilized or Liquid

浓    度 :  1mg/ml

免 疫 原 :  KLH conjugated synthetic peptide derived from human METTL15/METT5D1:321-407/407

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 :  METT5D1 is a 407 amino acid protein that is thought to function as an S-adenosyl-L-methionine-dependent methyltransferase. Existing as four alternatively spliced isoforms, METT5D1 belongs to the RsmH family and methyltransferase superfamily. The gene encoding METT5D1 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

Function:

Probable S-adenosyl-L-methionine-dependent methyltransferase.

Similarity:

Belongs to the methyltransferase superfamily. RsmH family.

SWISS:

A6NJ78

Gene ID:

196074

Important Note:

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.